Dissertations / Theses on the topic 'Parthenogenesis'
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Park, Arum. "Parthenogenesis in Hesiod’s Theogony." Penn State University Press, 2014. http://hdl.handle.net/10150/622192.
Full textAbbas, Nasser. "Parthenogenesis in plants: putative functions of MCM genes." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964450941.
Full textGoudie, Frances. "The Evolutionary Genetics of Thelytokous Parthenogenesis in Eusocial Hymenoptera." Thesis, The University of Sydney, 2014. http://hdl.handle.net/2123/13632.
Full textLundmark, Magnus. "Evolution of asexuality in insects : Polyploidy, hybridization and geographical parthenogenesis." Doctoral thesis, Umeå : Department of Molecular Biology, Umeå University, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-980.
Full textKumati, Osama B. Mohamed. "Virus life cycle and the parthenogenesis of malignant catarrhal fever." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/38034/.
Full textGriffin, Clare Louise, and clare griffin@flinders edu au. "A comparison of the ecology and behaviour of parthenogenetic and sexual taxa of the Australian skink, Menetia greyii: implications for coexistence." Flinders University. School of Biological Sciences, 2006. http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20070202.132116.
Full textSpence, Jennifer M. "Repetitive DNA in aphids : its nature, chromosomal distribution and evolutionary significance." Thesis, University of Reading, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298517.
Full textLaw, Jennifer Heather. "The evolution of geographic parthenogenesis and the persistence of asexuality in Timema walking-sticks." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ61577.pdf.
Full textBall, Shelley L. "Evolutionary ecology and population genetics of tychoparthenogenesis in the mayfly, Stenonema femoratum (Ephemeroptera:Heptageniidae) /." free to MU campus, to others for purchase, 2000. http://wwwlib.umi.com/cr/mo/fullcit?p9988643.
Full textTrakalo, Joseph Mark. "The impact of obligate parthenogenesis on concerted evolution of the rDNA IGS in populations of Daphnia pulex." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ56375.pdf.
Full textMcGee, Rob. "Allelism and allele sequence divergence of LOP, the locus of parthenogenesis in the model apomict Hieracium praealtum (Asteraceae)." Thesis, University of Canterbury. School of Biological Sciences, 2013. http://hdl.handle.net/10092/8984.
Full textKuhn, Alexandre. "Origin and evolution of social hybridogenesis in Cataglyphis ants: Origine et évolution de l'hybridogenèse sociale chez les fourmis Cataglyphis." Doctoral thesis, Universite Libre de Bruxelles, 2019. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/287547.
Full textL’hybridation et l’introgression génétique jouent un rôle majeur dans l’adaptation et ladiversification des espèces. Chez les fourmis du désert du genre Cataglyphis, certaines espècesont évolué une stratégie de reproduction remarquable, appelée hybridogenèse sociale, reposantsur l’hybridation systématique entre deux lignées génétiquement distinctes. Les ouvrières nonreproductricessont issues de l’accouplement entre des partenaires de lignées distinctes ;enrevanche, les reines et les mâles sont produits de façon asexuée par parthénogenèse. Lesouvrières sont donc toutes des hybrides des deux lignées, alors que les individus reproducteurssont de pure-lignées. Bien que plusieurs études aient analysé les stratégies de reproduction desfourmis Cataglyphis, l’origine et le fonctionnement de l’hybridogenèse sociale au sein du genrerestent obscurs.Dans cette thèse, trois aspects associés au maintien de ce système ont premièrement étéétudiés en prenant la fourmi Cataglyphis mauritanica comme modèle. (i) La forte associationentre génotype et caste des femelles est lié à une forte influence génétique sur le déterminismede la caste. Néanmoins, une certaine plasticité phénotypique est maintenue dans les génomeshybrides et pure-lignée mais elle ne s’exprime pas en conditions naturelles. (ii) L’analysegénétique d’une population hybridogène de C. mauritanica montre que les deux lignées sontéquifréquentes. De plus, une dispersion limitée des reines ainsi que leur production parparthénogenèse mènent à la formation d’une mosaïque de patches clonaux. A l’inverse, lesmâles dispersent d’un patch à l’autre assurant les accouplements interlignées. (iii) Afin dedéterminer si les accouplements intralignées participent à la production des reines, des donnéesgénétiques ont été simulées sous différents taux de reproduction sexuée et asexuée. Les résultatsmontrent que la diversité génétique au sein de chaque lignée correspond à une faible fréquencede reproduction sexuée, bien que qu’un scénario avec 100% de clonalité ne puisse être écarté.Ensuite, l’origine évolutive de l’hybridogenèse sociale chez les Cataglyphis a étéanalysée. L’étude des systèmes reproducteurs de 11 espèces de Cataglyphis a permis ladécouverte de 5 nouveaux systèmes hybridogènes. Des analyses phylogénétiques, basées surces espèces et sur toutes les espèces de Cataglyphis pour lesquels le système reproducteur a étéprécédemment étudié, indiquent que ce système reproducteur aurait évolué plusieurs foisindépendamment au sein du genre Cataglyphis.En conclusion, les résultats de cette thèse soulignent les singularités d’un systèmehybridogène associé à la parthénogénèse des reines, qui a pu faciliter l’évolution répétée delignées dépendantes chez les fourmis Cataglyphis.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Hanson, Sara Jeanette. "The molecular evolution of reproduction in animals: insights from sexual and asexual rotifers." Diss., University of Iowa, 2013. https://ir.uiowa.edu/etd/1618.
Full textRey, Olivier. "Systèmes de reproduction et scénarios d’invasion chez la petite fourmi de feu, Wasmannia auropunctata." Electronic Thesis or Diss., Montpellier, SupAgro, 2011. http://www.theses.fr/2011NSAM0046.
Full textThe main goal of this thesis is to provide new insights on the evolutionary processes associated to biological invasions through the study of invasive and non-invasive populations of the little fire ant, W. auropunctata. This species is characterised by an eccentric breeding system polymorphism. In ancestral populations, queens and males reproduce following the classical sexual reproduction system of hymenopteran species (haplo-diploid). In some other populations, queens reproduce by parthenogenesis and the males are reproduced clonally through queens' eggs. These clonal queens and males nevertheless produce sterile workers sexually. Interestingly this clonal reproduction seems indirectly associated with the invasive success of populations. In this study, we first identified the mechanisms underlying the breeding system of clonal populations. Our results indicate that queens use automictic parthenogenesis associated with a drastic reduction of meiotic recombination rate, androgenesis and sexual reproduction for the production of queens, males, and sterile workers respectively. The fixation of parental genomes in the successive generations allows individuals from the same cohort to reproduce together avoiding inbreeding depression in their worker offspring. We also found that the change of breeding system from sexuality to clonality is associated with an adaptive change that allow workers from clonal populations to better tolerate the stressing temperatures of invaded areas better than workers from ancestral sexual populations. Finally, we used a developed mutlidisciplinary approach combining niche modelling, genetic analyses and laboratory experiments, and found that the above evolutionary changes occur within the native range in marginal habitats prior to long-distance dispersal events into localities that display similar environmental conditions
Taylor, Alison Sandra. "Human parthenogenesis : an investigation to determine whether human parthenogentic embryos can be used as an alternative model for embryo research." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244020.
Full textVandervoort, Carla Louise. "Geographic parthenogenesis: A case study of sexual and apomictic Erigeron strigosus Muhl. ex Willd. (prairie fleabane) in the southeastern United States." Diss., Connect to online resource, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1433499.
Full textPorciuncula, Patrícia Marafon. "Ativação partenogenética de oócitos bovinos jovens com ionomicina e 6-dimetilaminopurina associado ou não ao estrôncio." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/74/74131/tde-14112007-155048/.
Full textConsidering the possibility of the combination of different activating agents associated to the influence of oocyte ageing on embryo development, the purpose of this work to study the relationship between oocyte ageing and parthenogenetic activation. Bovine oocytes were in vitro maturated for 22 (young) and 28 h (aged). Next, both groups of oocytes were activated using the following treatments: ID3: ionomycin (5 µM for 5 min) + 6DMAP (2 mM for 3 h); ID6: ionomycin (5 µM for 5 min) + 6DMAP (2 mM for 6 h); IDS: ionomicyn + 6DMAP (2 mM) and strontium (20 mM; SrCl2) for 6 h and IDSS: ionomicyn + (6DMAP+Sr2+) for the first 3h, followed by incubation with Sr2+ alone for another 3 h. The control group was cultured in the absence of any activating agents (spontaneous activation). After activation, the oocytes were evaluated for: 1) activation rate (pronuclei formation at 12 hpa); 2) activity of maturation promoting factor (MPF) and mitogen activated protein kinase (MAPK) at 5 min, 3 h, 6 h and 10 hpa; 3) embryo development (cleavage rate at 48 h and blastocyst and hatching rates on days 7 and 9); 4) embryo quality (day 9 regarding total cell numbers, apoptosis and interferon-t expression). In general, young oocytes showed lower activation rates and higher MPF and MAPK activity when compared with aged oocytes. However, incubation of the oocytes with 6DMAP for 6 h allowed development rates similar to aged oocytes with a small decrease in total cell number, but without effects on other criteria of embryo quality. The data suggest a possible application of these results in such a way to contribute for timing flexibilization in NT experiments and production of good quality embryos.
Miyauchi, Tochimara Aparecida. "Aspectos biológicos do desenvolvimento pré- implantacional de embriões bovinos partenogenéticos ou fecundados in vitro." Universidade Jose do Rosario Vellano, 2012. http://tede2.unifenas.br:8080/jspui/handle/jspui/140.
Full textCoordenacao de Aperfeicoamento de Pessoal de Nïvel Superior
Parthenogenesis has been described as an alternative method to produce embryos for studies with embryonic cells, particularly in humans which have a restriction of fertilized embryos. Procedures used in parthenogenesis are also required to produce embryos by somatic cell nuclear transfer in domestic species. However, many biological, cellular and molecular aspects of parthenogenetic embryos are still unknown. This study aimed to compare the kinetics of development, apoptosis rate and gene expression of stress and celular metabolism in bovine parthenogenetic embryos and embryos fertilized in vitro. Oocytes (n = 1541) obtained from slaughterhouse ovaries were matured in vitro and submitted to parthenogenetic activation (4.62 µM ionomycin for 5 min followed by 2 mM 6-DMAP for 4 h) or in vitro fertilization (2 x 106 sperm/mL for 20h with semen from a single departure). 72h postactivation/fertilization (hpaf), embryos (8-cell) were frozen for subsequent analysis of gene expression and another part has been separated into groups of high or low potential of development: Part ≥ 8 - parthenogenetic embryos with 8 or more cells (high development potential); Part < 8 - embryos less than 8 cells (low development potential); ≥ 8 IVF - in vitro fertilized embryos with 8 or more cells; and IVF < 8 - embryos with less than 8 cells. Embryos were cultured in CR2aa medium with 2.5% BFS in 5% CO2, 5% O2, 90% N2 at 38.5° C and were evaluated rates of blastocyst 168hpaf (D7) and 196hpaf (D8). 8-cell embryos obtained after 72hpfa were analyzed for gene expression. D8 blastocysts were fixed and subsequently apoptotic index was analyzed by TUNEL. Data were compared by analysis of variance and means by Student Newman Keuls test. Gene expression was evaluated by REST® software. Values are shown as mean ± standard error. Embryos with 8 or more cells produced higher (P < 0.01) blastocysts rates in D7 and D8 compared to embryos with less than eight cells, showing its greatest development potential, regardless if they were parthenogenetic or fertilized. Embryos of Part ≥ 8 group had higher (P <0.05) blastocyst rate in D7 (63.6 ± 3.4%) than IVF ≥ 8 (45.3 ± 8.9%), but at D8 rate was similar (56.7 ± 3.0% and 44.2 ± 8.9% for Part ≥ 8 and IVF ≥ 8, respectively; P <0.05). There was no difference (P < 0.05) on blastocyst rates at D7 and D8 between embryos with less than 8 cells derived from parthenogenesis or fertilization. There was no difference in total cell number (92.0 ± 3.4, 102.30 ± 4.8), apoptotic cells (10.8 ± 1.22, 9.5 ± 1.07) and apoptotic index (11.4 ± 1.27, 9.8 ± 1.8) for parthenogenetic and IVF blastocysts, respectively. In 8-cell embryos analyzed, there was a subexpression of genes DNAJB1, HSPA1L, HSF1 and GLUT1 for Part in relation to FIV, while HSF2 was overexpressed in Part compared to FIV. In conclusion, bovine parthenogenetic embryos differ to embryos fertilized in vitro in hability of preimplantation development in vitro and gene expression, which may limit the use of parthenogenesis in studies of embryonic development.
A partenogênese tem sido descrita como um método alternativo para produzir embriões para estudos com células embrionárias, principalmente em humanos para os quais existe a restrição do uso de embriões fecundados. Procedimentos utilizados na partenogênese são também necessários para se produzir embriões por transferência nuclear com células somáticas nas espécies domésticas. Contudo, muitos aspectos biológicos, celulares e moleculares dos embriões partenogenéticos ainda são desconhecidos. Este estudo objetivou comparar a cinética do desenvolvimento, índice de apoptose e expressão de genes de estresse e metabolismo celular em embriões bovinos partenogenéticos e embriões fecundados in vitro. Oócitos (n=1541) obtidos de ovários de matadouro foram maturados in vitro e submetidos à ativação partenogenética (4,62 µM ionomicina por 5 min seguido de 2 mM 6-DMAP por 4h) ou fecundação in vitro (2 x 106 espermatozoides/ml por 20h, com sêmen de uma única partida). Com 72h pós-ativação/fecundação (hpaf) parte dos embriões (8 células) foram congelados para posterior análise da expressão gênica e outra parte foi separada em grupos de alto ou baixo potencial de desenvolvimento: Part≥8 - embriões partenogenéticos com 8 ou mais células (alto potencial de desenvolvimento); Part<8 - embriões com menos de 8 células (baixo potencial de desenvolvimento); FIV≥8 - embriões fecundados in vitro com 8 ou mais células; e FIV<8: embriões com menos de 8 células. Os embriões foram cultivados em meio CR2aa com 2,5% SFB em 5%CO2, 5%O2, 90% N2 a 38,5ºC e avaliadas as taxas de blastocistos com 168hpaf (D7) e 196hpaf (D8). Embriões com 8 células obtidos após 72hpfa foram analisados quanto à expressão gênica. Blastocistos em D8 foram fixados e posteriormente foram avaliados pela técnica de TUNEL o índice apoptótico. Os dados foram comparados por análise de variância e as médias por teste de Student Newman Keuls. A expressão gênica foi avaliada pelo software REST®. Os valores são mostrados como média±erro padrão. Embriões com 8 ou mais células produziram maiores (P<0,01) taxas de blastocistos no D7 e D8 do que os embriões com menos de oitos células mostrando seu maior potencial de desenvolvimento, independentemente se foram partenogenéticos ou fecundados. Embriões do grupo Part≥8 apresentaram maior (P<0,05) taxa de blastocistos no D7 (63,6±3,4%) que os FIV≥8 (45,3±8,9%), porém a taxa no D8 foi semelhante (56,7±3,0% e 44,2±8,9% para Part≥8 e FIV≥8, respectivamente; (P<0,05). Não houve diferença (P<0,05) quanto às taxas de blastocistos no D7 e D8 entre embriões com menos de 8 células oriundos da partenogênese ou fecundação. Não houve diferença quanto ao número total de células (92,0±3,4; 102,30±4,8), células apoptóticas (10,8±1,22; 9,5±1,07) e índice apoptótico (11,4±1,27; 9,8±1,8) nos blastocistos partenogenéticos e FIV, respectivamente. Nos embriões com 8 células analisados, houve subexpressão dos genes DNAJB1, HSPA1L, HSF1, GLUT1 nos Part em relação aos FIV, enquanto o HSF2 esteve sobrexpresso nos Part quando comparado aos FIV. Conclui-se que embriões partenogenéticos bovinos possuem diferenças se comparados aos embriões fecundados in vitro quanto à capacidade de desenvolvimento pré-implantacional in vitro e expressão gênica, o que pode limitar o uso da partenogênese em estudos sobre desenvolvimento embrionário.
Pearcy, Morgan. "Stratégies reproductrices chez la fourmi Cataglyphis cursor." Doctoral thesis, Universite Libre de Bruxelles, 2005. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210909.
Full textKin selection is, to date, the most widely accepted theory to justify the evolution of a sterile worker caste among social Hymenoptera. The Mediterranean ant Cataglyphis cursor represents an interesting biological model for several reasons, the most important of them being the ability for unmated workers to produce haploid (male) offspring, through arrhenotokous parthenogenesis, and diploid (female) offspring, through thelytokous parthenogenesis. Our genetic analyses, based on microsatellite loci developed for this purpose, revealed that queens selectively use sexual and asexual reproduction to produce workers and sexuals, respectively. Pedigree analyses allowed us to identify the cytological mechanism involved in thelytokous parthenogenesis and to estimate the proportion of worker-produced queens in the study population. Although C. cursor queens do not require mating to produce diploid offspring, they have retained sexual reproduction and mate multiply with up to 8 males. This suggests that sexual reproduction has important benefits for colony function, and we tested several hypotheses accounting for the evolution of polyandry. Eventually, we studied the effect of dispersal strategies on sex-ratio of the sexual brood. These results confirm the interest of investigating the reproductive strategies of social Hymenoptera to test the predictions of diverse theories in the field of evolutionary biology, and open new research perspectives in C. cursor and other ants of the Cataglyphis genera.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Rascado, Tatiana da Silva [UNESP]. "Produção de embriões por fecundação in vitro e ativação partenogenética visando o isolamento de células tronco embrionárias felinas." Universidade Estadual Paulista (UNESP), 2009. http://hdl.handle.net/11449/94582.
Full textFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
O objetivo deste estudo foi aprimorar os protocolos de produção in vitro de embriões e de ativação partenogenética visando o isolamento e o cultivo de células tronco embrionárias felinas. Os CCOs-I foram obtidos a partir de ovários de gatas adultas e maturados in vitro. No experimento I, os CCOS foram fecundados e os embriões cultivados nos meios SOFaa e FOC. Foram comparadas as taxas de clivagem e a produção de blastocistos. A análise estatística foi realizada por meio da análise de variância e a viabilidade embrionária foi avaliada por sondas fluorescentes (Hoechst e iodeto de propídio). Não houve diferenças significativas entre os meios de cultivo, os quais apresentaram taxas de clivagem de 50,5±9,47 e 63,75±5,9 (P>0,05) e de produção de blastocistos em relação ao total de oócitos fecundados de 18±5,07 e 33,2±3,71 (P>0,05) para FOC e SOF respectivamente. No experimento II, os CCOs maturos foram submetidos a três diferentes protocolos de ativação partenogenética: 1-ionomicina associada ao cicloheximide; 2-ionomicina associada ao roscovitine e 3-ionomicina associada ao estrôncio, os quais foram comparados entre si e ao controle quanto às taxas de ativação, clivagem e desenvolvimento embrionário, sendo cultivados em SOFaa por 72 horas após a ativação. Para tais avaliações, oócitos e embriões foram corados com Hoechst 33342 e examinados em microscópio invertido. Como análise estatística foi utilizado o teste qui-quadrado. Não houve diferença significativa entre os tratamentos quanto à taxa de oócitos ativados (69,9%, 76,6% e 64,6%, para tratamento 1, 2 e 3 respectivamente) (P>0,05) nem quanto às taxas de clivagem (46,6%, 46,73% e 32,32%, para tratamento 1, 2 e 3 respectivamente) (P>0,05), mas sim entre estes e o controle (36% e 12%, respectivamente, para taxa de oócitos ativados e taxas de clivagem) (P<0,05). Quanto ao desenvolvimento...
The objective of this study was to improve the existent protocols for in vitro embryos production and parthenogenetic activation in cats, aiming the isolation and culture of feline embryonic stem cells. COCs-I were collected from adult queens´s ovaries and matured in vitro. In the experiment I, COCs were fertilized and embryos cultured in two culture media, SOFaa and FOC. In both media the cleavage rate and blastocysts production were compared. Fluorescents probes (Hoechst and propidium iodide) were utilized to estimate embryo viability. The statistical analysis was realized through the ANOVA. No statistical difference was observed between culture media. The cleavage rates considering the total number of fertilized oocytes were 50.5±9.47 and 63.75±5.9 (P>0.05) for FOC and SOF medium respectively. Similarly, the blastocysts production rates were 18±5.07 and 33.2±3.71 (P>0.05) for FOC and SOF, respectively. In experiment II matured COCs were submitted to three parthenogenetic activation protocols: 1- ionomycin associated to cycloheximide; 2 – ionomycin associated to roscovitine; 3 – ionomycin associated to strontium. The treatments were compared among themselves and among them and the control concerning chromatin decondensation, cleavage and embryo development rates. The parthenogenetic embryos were then cultured in SOFaa during 72 hours. To estimate chromatin status and number of nuclei, oocytes and embryos were stained with Hoechst 33342 and examined under an inverted fluorescent microscope. As statistical analyses chi-square test was utilized. No statistical difference was observed among treatments concerning activated oocytes rates (69.9%, 76.6% e 64.6%, respectively, for treatment 1, 2 and 3) (P>0.05) neither cleavage rates (46.6%, 46.73% e 32.32%, respectively, for treatment 1, treatment 1, 2, 3) (P>0.05). However, statistical difference was observed among treatments and... (Complete abstract click electronic access below)
Mathias, Frank Furlong Jr. "A Plio-Pleistocene Record of Lacustrine Ostracodes from Butte Valley, California: Faunal Responses to Tectonic and Climatic Change." Kent State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=kent1404725598.
Full textSmith, Hilary April. "Evolution of Reproduction and Stress Tolerance in Brachionid Rotifers." Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/52145.
Full textBem, Tiago Henrique Camara De. "Efeito da pré-maturação sobre o desenvolvimento embrionário de oócitos submetidos à ativação partenogenética e transferência de núcleo." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/74/74131/tde-08092009-114443/.
Full textEmbryo production rates obtained from both IVF (30-40%) and NT (23%) are still below the expected values. Therefore, oocyte pre-maturation using cell cycle inhibitors is one of the alternatives which has been studied to increase the competence of oocytes used for IVP, as an attempt to optimize the success rates of these biotechniques. Neurotrophins are known to play several roles in the reproductive system. BDNF is an example of a neurotrophin that seems to be related to oocyte maturation. Therefore, the objective of this study was to improve techniques of pre-maturation and maturation of bovine oocytes submitted to parthenogenetic activation, aiming for its use on cloning by nuclear transfer. Bovine oocytes were submitted to maturation either in presence (IVM/BD) or absence (IVM) of BDNF or pre-matured with BLI and supplemented (BL/BD) or not (BL) with the neurotrophin. Groups were evaluated for maturation rates (metaphase II), activation (pro-nucleus formation) and embryo development (blastocyst formation rate and quality). There was no difference (P>0.05) in MII rate after the maturation with or without BDNF. However, pre-maturation in the supplemented group (BL/BD, n=73; 91.2%) resulted in higher MII rate (P<0.05) when compared with the nonsupplemented group (BL, n=66; 76.7%). Oocytes which were matured under the same conditions were also activated chemically for embryonic development analysis. Activation rates were different (P<0.05) from IVM/BD groups (n=30; 71.4%) and IVM (n=41; 91.1%). However, no difference were observed for development parameters. When the oocytes were prematured, cleavage rates in the supplemented group were superior (P<0.05) than non supplemented group (BL/BD: n=227; 65.2%) and (BL: n=187; 57.7%), but no difference was observed for other developmental parameters. Embryo quality was also evaluated and no difference was observed between treatments. Groups submitted to NT (IVM and BL/BD) differed regarding (P<0.05) the 1stPB extrusion (n=639; 63.5% and n=693; 69.5%, respectively) and fusion rate (n=345; 72.9% and n=397; 79.2%, respectively), but did not present differences for other evaluated parameters. Embryo quality was evaluated again and no differences were observed. After the embryos were transferred to recipient cows, groups IVM (n=3; 10.7%) and BL/BD (n=3; 11.5%) were capable of producing advanced gestations at similar rates (P>0.05). Based on these results, it may be concluded that supplementation of both maturation and pre-maturation does not impair embryonic development. Additionally, cloned embryos produced from blocked oocytes are able to establish advanced gestation in cattle.
Jackson, Heather Bird. "Distribution of chemistry and sexual fecundity in the lichenized-fungi, Xanthoparmelia cumberlandia and Xanthoparmelia coloradoensis on Boulder Mountain, Aquarius Plateau, UT." BYU ScholarsArchive, 2004. https://scholarsarchive.byu.edu/etd/206.
Full textRey, Olivier. "Systèmes de reproduction et scénarios d’invasion chez la petite fourmi de feu, Wasmannia auropunctata." Thesis, Montpellier, SupAgro, 2011. http://www.theses.fr/2011NSAM0046/document.
Full textThe main goal of this thesis is to provide new insights on the evolutionary processes associated to biological invasions through the study of invasive and non-invasive populations of the little fire ant, W. auropunctata. This species is characterised by an eccentric breeding system polymorphism. In ancestral populations, queens and males reproduce following the classical sexual reproduction system of hymenopteran species (haplo-diploid). In some other populations, queens reproduce by parthenogenesis and the males are reproduced clonally through queens' eggs. These clonal queens and males nevertheless produce sterile workers sexually. Interestingly this clonal reproduction seems indirectly associated with the invasive success of populations. In this study, we first identified the mechanisms underlying the breeding system of clonal populations. Our results indicate that queens use automictic parthenogenesis associated with a drastic reduction of meiotic recombination rate, androgenesis and sexual reproduction for the production of queens, males, and sterile workers respectively. The fixation of parental genomes in the successive generations allows individuals from the same cohort to reproduce together avoiding inbreeding depression in their worker offspring. We also found that the change of breeding system from sexuality to clonality is associated with an adaptive change that allow workers from clonal populations to better tolerate the stressing temperatures of invaded areas better than workers from ancestral sexual populations. Finally, we used a developed mutlidisciplinary approach combining niche modelling, genetic analyses and laboratory experiments, and found that the above evolutionary changes occur within the native range in marginal habitats prior to long-distance dispersal events into localities that display similar environmental conditions
Erdmann, Georgia. "Community structure, trophic ecology and reproductive mode of oribatid mites (Oribatida, Acari) in forest ecosystems." Thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2012. http://hdl.handle.net/11858/00-1735-0000-000C-B7E7-7.
Full textPhilipp, H. Schiffer [Verfasser], Einhard [Akademischer Betreuer] Schierenberg, and Guenter [Akademischer Betreuer] Plickert. "A genomic perspective on variations in the molecular toolkit for development and on the evolution of parthenogenesis in Nematoda / Schiffer Philipp H.. Gutachter: Einhard Schierenberg ; Guenter Plickert." Köln : Universitäts- und Stadtbibliothek Köln, 2015. http://d-nb.info/1069985821/34.
Full textRascado, Tatiana da Silva. "Produção de embriões por fecundação in vitro e ativação partenogenética visando o isolamento de células tronco embrionárias felinas /." Botucatu, 2009. http://hdl.handle.net/11449/94582.
Full textBanca: Maria Denise Lopes
Banca: Mayra Elena Ortiz D'Avila Assumpção
Resumo: O objetivo deste estudo foi aprimorar os protocolos de produção in vitro de embriões e de ativação partenogenética visando o isolamento e o cultivo de células tronco embrionárias felinas. Os CCOs-I foram obtidos a partir de ovários de gatas adultas e maturados in vitro. No experimento I, os CCOS foram fecundados e os embriões cultivados nos meios SOFaa e FOC. Foram comparadas as taxas de clivagem e a produção de blastocistos. A análise estatística foi realizada por meio da análise de variância e a viabilidade embrionária foi avaliada por sondas fluorescentes (Hoechst e iodeto de propídio). Não houve diferenças significativas entre os meios de cultivo, os quais apresentaram taxas de clivagem de 50,5±9,47 e 63,75±5,9 (P>0,05) e de produção de blastocistos em relação ao total de oócitos fecundados de 18±5,07 e 33,2±3,71 (P>0,05) para FOC e SOF respectivamente. No experimento II, os CCOs maturos foram submetidos a três diferentes protocolos de ativação partenogenética: 1-ionomicina associada ao cicloheximide; 2-ionomicina associada ao roscovitine e 3-ionomicina associada ao estrôncio, os quais foram comparados entre si e ao controle quanto às taxas de ativação, clivagem e desenvolvimento embrionário, sendo cultivados em SOFaa por 72 horas após a ativação. Para tais avaliações, oócitos e embriões foram corados com Hoechst 33342 e examinados em microscópio invertido. Como análise estatística foi utilizado o teste qui-quadrado. Não houve diferença significativa entre os tratamentos quanto à taxa de oócitos ativados (69,9%, 76,6% e 64,6%, para tratamento 1, 2 e 3 respectivamente) (P>0,05) nem quanto às taxas de clivagem (46,6%, 46,73% e 32,32%, para tratamento 1, 2 e 3 respectivamente) (P>0,05), mas sim entre estes e o controle (36% e 12%, respectivamente, para taxa de oócitos ativados e taxas de clivagem) (P<0,05). Quanto ao desenvolvimento... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: The objective of this study was to improve the existent protocols for in vitro embryos production and parthenogenetic activation in cats, aiming the isolation and culture of feline embryonic stem cells. COCs-I were collected from adult queens's ovaries and matured in vitro. In the experiment I, COCs were fertilized and embryos cultured in two culture media, SOFaa and FOC. In both media the cleavage rate and blastocysts production were compared. Fluorescents probes (Hoechst and propidium iodide) were utilized to estimate embryo viability. The statistical analysis was realized through the ANOVA. No statistical difference was observed between culture media. The cleavage rates considering the total number of fertilized oocytes were 50.5±9.47 and 63.75±5.9 (P>0.05) for FOC and SOF medium respectively. Similarly, the blastocysts production rates were 18±5.07 and 33.2±3.71 (P>0.05) for FOC and SOF, respectively. In experiment II matured COCs were submitted to three parthenogenetic activation protocols: 1- ionomycin associated to cycloheximide; 2 - ionomycin associated to roscovitine; 3 - ionomycin associated to strontium. The treatments were compared among themselves and among them and the control concerning chromatin decondensation, cleavage and embryo development rates. The parthenogenetic embryos were then cultured in SOFaa during 72 hours. To estimate chromatin status and number of nuclei, oocytes and embryos were stained with Hoechst 33342 and examined under an inverted fluorescent microscope. As statistical analyses chi-square test was utilized. No statistical difference was observed among treatments concerning activated oocytes rates (69.9%, 76.6% e 64.6%, respectively, for treatment 1, 2 and 3) (P>0.05) neither cleavage rates (46.6%, 46.73% e 32.32%, respectively, for treatment 1, treatment 1, 2, 3) (P>0.05). However, statistical difference was observed among treatments and... (Complete abstract click electronic access below)
Mestre
Vollmer, Alicia A. "Rare Parthenogenic Reproduction in a Common Reef Coral, Porites astreoides." Thesis, NSUWorks, 2018. https://nsuworks.nova.edu/occ_stuetd/464.
Full textDuke, Connor Raymond. "Optimization of Control Source and Error Sensor Locations in Free Field Active Noise Control." BYU ScholarsArchive, 2007. https://scholarsarchive.byu.edu/etd/1169.
Full textSherwood, David Alan. "A Simple Metabolic Switch May Activate Apomixis in Arabidopsis thaliana." DigitalCommons@USU, 2018. https://digitalcommons.usu.edu/etd/7409.
Full textNiciura, Simone Cristina Méo. "Interação núcleo-citoplasmática em embriões e expressão de genes "imprinted" em fetos bovinos produzidos in vivo, in vitro e partenogenéticos /." Jaboticabal : [s.n.], 2005. http://hdl.handle.net/11449/105949.
Full textBanca: Flávio Vieira Meirelles
Banca: Claudia Lima Verde Leal
Banca: Vera Fernanda Martins Hossepian de Lima
Banca: Gisele Zoccal Mingoti
Resumo: A maturação oocitária é marcada pela retomada da primeira divisão da meiose, com progressão do estádio de Vesícula Germinativa (GV) da Prófase I até a Metáfase II (MII), e inclui todos os eventos necessários para que o oócito expresse seu potencial máximo de desenvolvimento após a fecundação. Para avaliarmos a eficiência da maturação in vitro (MIV), utilizamos oócitos classificados em viáveis (graus I, II e III) e inviáveis (atrésico e desnudo), e acompanhamos a progressão nuclear e a distribuição dos grânulos corticais (GC) como indício de maturação citoplasmática, após MIV em TCM 199 com soro fetal bovino, hormônios, antibiótico e piruvato, por 24h em 5% de CO2 em ar. Maturação nuclear (78,4-87,8%) e citoplasmática (GC periféricos; 67,2-79,3%) foram semelhantes entre as diferentes classes de oócitos e apresentaramse como eventos independentes. Para o acompanhamento dos eventos desencadeados pelo espermatozóide, avaliamos a dinâmica nuclear e de microtúbulos, em intervalos de 2h, após fecundação in vitro (FIV), em meio TALP com heparina, PHE e sêmen preparado em gradiente de Percoll. Observamos que o estádio de MII foi predominante de 2 a 8h; MII e Anáfase/Telófase (A/T) predominaram às 10h; MII, A/T e estádio pronuclear (PN) de 14 a 16h; e PN a partir de 18h. A penetração do espermatozóide ocorreu após 4h da inseminação dos oócitos; a diferenciação dos PN 14 masculino e feminino pelo tamanho foi possível de 14 a 18h e a singamia ocorreu a partir de 24h. O período de 10h pode ser suficiente para que a FIV seja efetiva em oócitos bovinos, nas condições aqui descritas.
Abstract: We aimed to evaluate events involved in in vitro maturation, fertilization and development, and parthenogenetic activation of bovine oocytes assessed by nuclear-cytoplasmic interaction and gene expression. Oocyte morphological selection did not affect nuclear maturation (78.4-87.8%) and cytoplasmic cortical granule distribution (67.2-79.3%). Following nuclear and microtubular dynamics after fertilization (IVF), we observed sperm penetration 4h after insemination; male and female pronuclei differentiation by size from 14 to 18h; syngamy after 24h; and sufficient co-incubation of spermatozoa and oocytes for 10h. Pronuclear transfer to study the interaction between nucleus (N) and cytoplasm (C) in parthenogenetic embryos produced by ionomycin followed by strontium (S) or 6-DMAP (D) was assessed by cleavage, eight-cell, and blastocyst development rates: CSND (76.5, 36.4, and 6.8%) and CDNS (69.5, 25.0, and 4.9%). S cytoplasm promoted dominant effect on D nucleus. Higher rates of developmental arrest up to the eight-cell stage were observed by the combination of cytoplasm and nucleus produced by the two different activation treatments. We recovered parthenogenetic D fetuses on Day 35, which were small but normal in formation and in appearance of chorio-alantoic membranes. Genomic imprinting of IGF2 was observed, but XIST was maternally expressed in extra-embryonic tissues. In vitro culture promoted higher expression of IGF2 and H19 genes and also increased IGF2/IGF2r ratio in IVF embryos compared to in vivo produced ones.
Doutor
Niciura, Simone Cristina Méo [UNESP]. "Interação núcleo-citoplasmática em embriões e expressão de genes imprinted em fetos bovinos produzidos in vivo, in vitro e partenogenéticos." Universidade Estadual Paulista (UNESP), 2005. http://hdl.handle.net/11449/105949.
Full textFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
A maturação oocitária é marcada pela retomada da primeira divisão da meiose, com progressão do estádio de Vesícula Germinativa (GV) da Prófase I até a Metáfase II (MII), e inclui todos os eventos necessários para que o oócito expresse seu potencial máximo de desenvolvimento após a fecundação. Para avaliarmos a eficiência da maturação in vitro (MIV), utilizamos oócitos classificados em viáveis (graus I, II e III) e inviáveis (atrésico e desnudo), e acompanhamos a progressão nuclear e a distribuição dos grânulos corticais (GC) como indício de maturação citoplasmática, após MIV em TCM 199 com soro fetal bovino, hormônios, antibiótico e piruvato, por 24h em 5% de CO2 em ar. Maturação nuclear (78,4-87,8%) e citoplasmática (GC periféricos; 67,2-79,3%) foram semelhantes entre as diferentes classes de oócitos e apresentaramse como eventos independentes. Para o acompanhamento dos eventos desencadeados pelo espermatozóide, avaliamos a dinâmica nuclear e de microtúbulos, em intervalos de 2h, após fecundação in vitro (FIV), em meio TALP com heparina, PHE e sêmen preparado em gradiente de Percoll. Observamos que o estádio de MII foi predominante de 2 a 8h; MII e Anáfase/Telófase (A/T) predominaram às 10h; MII, A/T e estádio pronuclear (PN) de 14 a 16h; e PN a partir de 18h. A penetração do espermatozóide ocorreu após 4h da inseminação dos oócitos; a diferenciação dos PN 14 masculino e feminino pelo tamanho foi possível de 14 a 18h e a singamia ocorreu a partir de 24h. O período de 10h pode ser suficiente para que a FIV seja efetiva em oócitos bovinos, nas condições aqui descritas.
We aimed to evaluate events involved in in vitro maturation, fertilization and development, and parthenogenetic activation of bovine oocytes assessed by nuclear-cytoplasmic interaction and gene expression. Oocyte morphological selection did not affect nuclear maturation (78.4-87.8%) and cytoplasmic cortical granule distribution (67.2-79.3%). Following nuclear and microtubular dynamics after fertilization (IVF), we observed sperm penetration 4h after insemination; male and female pronuclei differentiation by size from 14 to 18h; syngamy after 24h; and sufficient co-incubation of spermatozoa and oocytes for 10h. Pronuclear transfer to study the interaction between nucleus (N) and cytoplasm (C) in parthenogenetic embryos produced by ionomycin followed by strontium (S) or 6-DMAP (D) was assessed by cleavage, eight-cell, and blastocyst development rates: CSND (76.5, 36.4, and 6.8%) and CDNS (69.5, 25.0, and 4.9%). S cytoplasm promoted dominant effect on D nucleus. Higher rates of developmental arrest up to the eight-cell stage were observed by the combination of cytoplasm and nucleus produced by the two different activation treatments. We recovered parthenogenetic D fetuses on Day 35, which were small but normal in formation and in appearance of chorio-alantoic membranes. Genomic imprinting of IGF2 was observed, but XIST was maternally expressed in extra-embryonic tissues. In vitro culture promoted higher expression of IGF2 and H19 genes and also increased IGF2/IGF2r ratio in IVF embryos compared to in vivo produced ones.
Lashermes, Philippe. "Gynogenese et androgenese in vivo chez le mais (zea mays l. ) : etudes genetique et physiologique, utilisation en selection." Clermont-Ferrand 2, 1987. http://www.theses.fr/1987CLF21058.
Full textTimmermans, Iris. "Stratégies de reproduction au sein du genre Cataglyphis (Hymenoptera :Formicidae): analyse comparative." Doctoral thesis, Universite Libre de Bruxelles, 2009. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210238.
Full textLes travaux réalisés dans le cadre de cette thèse de doctorat visent à déterminer si les stratégies reproductrices remarquables exploitées par C. cursor sont propres à l’espèce ou si elles ont évolué au sein de plusieurs espèces du genre. A cette fin, nos recherches s'articulent autour de 2 axes complémentaires. Premièrement, nous avons approfondi l'étude des stratégies reproductrices chez C. cursor en nous concentrant sur deux aspects. (i) Plusieurs hypothèses ont été proposées pour justifier l’évolution de la polyandrie chez les fourmis. Nos travaux ont testé et éliminé trois d’entre elles pour C. cursor :l’hypothèse de la limitation spermatique, celle des coûts des mâles diploïdes et celle selon laquelle une plus grande variabilité génétique des ouvrières améliorerait la division du travail. (ii) Nous avons mis en évidence l’existence d’un contrôle des reines dans le déterminisme de la caste chez cette espèce. Les reines ne produisent des œufs thélytoques qu’au début du printemps, lorsque les ouvrières élèvent les œufs en sexués. Plus tard dans la saison, les reines ne produisent plus que des œufs fertilisés qui se développeront en ouvrières.
Deuxièmement, à titre comparatif, nous avons analysé la structure socio-génétique de deux autres espèces de Cataglyphis :C. sabulosa et C. livida. Ces deux espèces sont monogynes et polyandres. Leurs ouvrières sont capables de pondre des œufs haploïdes mais seules les ouvrières de C. sabulosa ont produits des œufs diploïdes thélytoques. Aucune des reines des deux espèces n’utilisent la parthénogenèse thélytoque pour produire des femelles sexuées.
L’ensemble des résultats obtenus dans notre étude ont été replacés dans une perspective évolutive afin de préciser quand la polygynie, la polyandrie et la thélytoquie seraient apparues dans la phylogénie des Cataglyphis.
Doctorat en Sciences
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Mezzalira, Joana Claudia. "Efeito da heteroplasmia na densidade celular e desenvolvimento embrionário in vitro de embriões bovinos clonados por transferência nuclear de célula somática." Universidade do Estado de Santa Catarina, 2009. http://tede.udesc.br/handle/handle/892.
Full textCoordenação de Aperfeiçoamento de Pessoal de Nível Superior
In somatic cell nuclear transfer (SCNT), the type of the recipient cytoplast plays a key role on nuclear reprogramming. Distinct cytoplasts and karyoplasts and different activation protocols were used for bovine embryo cloning aiming to evaluate the effect of the type of cytoplast (oocyte and/or zygote) and the activation protocol (chemical, AQ, or spermatic, AE) on development of cloned blastocysts produced by handmade cloning (HMC). After 17 h of in vitro maturation (MIV), 2,946 oocytes were enucleated by manual bisection resulting in either MII cytoplasts (enucleated) or MII karyoplasts (non-enucleated). An additional group of 2,368 oocytes, in vitro-fertilized (FIV) for 6 h, were manually bisected and segregated in either FIV cytoplasts (enucleated) or FIV karyoplasts (non-enucleated). Cells from a primary culture previously established from a skin biopsy from an adult female bovine were used as nuclei donors (karyoplast CS). Structures were allocated to (a) control groups: FIV; parthenogenesis using zona-intact (PG c/) or zona-free oocytes (PG s/); and clones by SCNT; or (b) experimental groups: G1, FIV cytoplast + MII cytoplast + CS karyoplast; G2, MII cytoplast + FIV karyoplast; G3, FIV cytoplast + FIV karyoplast; G4, FIV cytoplast + FIV cytoplast + CS karyoplast; and G5, MII cytoplast + MII karyoplast. Following electrofusion, experimental groups G1 to G5 were allocated to sub-groups of either sperm-mediated (AE) or additional chemical (AQ) activation. The in vitro culture was carried out in the WOW (wellof- the-well) system. After 20 replications, cleavage (D2) and blastocyst (D7) rates were compared by the χ2 test, with values for total cell number and cell allocation in the blastocyst, determined by differential staining, being evaluated by ANOVA, with pairwise comparisons by the Tukey test, for P<0.05 (P<0.05). The only experimental group that yielded a blastocyst development similar to the FIV (27.0%) and SCNT (31.4%) control groups was the subgroup G1 AE (28.2%). This fact may be attributed to a more proper synchrony between the karyoplast and cytoplasts and/or to a more suitable activation process. Embryo development in subgroups G1 AQ (13.7%), G4 AQ (6.4%) and G4 AE (8.7%) was lower than in G1 AE, possibly due to a higher degree of asynchrony in the activation process or cell cycle. The lack of development in groups G2 and G3, irrespective of the activation protocol, was possibly due to the manipulation process during a highly sensible biological period. Likewise, the low cleavage (57.0%) and the lack of development in group G5 (spontaneous activation) in fact showed that the manipulation induced weak spontaneous oocyte activation. In general, total cell number and cell allocation were similar between groups with development to the blastocyst stage. In conclusion, the activation process appeared to be as important to embryo development as the type of cytoplast or karyoplast used for embryo reconstruction. The production of cloned bovine embryos using a more physiological activation process (AE) was proven as a viable procedure, with efficiency rates observed in subgroup G1 AE being similar to groups FIV or TNCS
Na clonagem por transferência nuclear com célula somática (TNCS), o tipo de citoplasto receptor desempenha papel chave na reprogramação nuclear. Distintos citoplastos e carioplastos e condições de ativação foram utilizadas na reconstrução de embriões bovinos com o objetivo de avaliar o efeito do tipo de citoplasto (oócito e/ou zigoto) e do método de ativação (química, AQ, ou espermática, AE) no desenvolvimento de blastocistos clonados produzidos pela técnica de clonagem manual (Handmade Cloning, HMC). Após 17 h de maturação in vitro (MIV), 2.946 oócitos foram enucleados por bissecção manual, resultando em hemi-oócitos enucleados (citoplastos MII) e não enucleados (carioplastos MII). Outros 2.368 oócitos submetidos a 6 h de fecundação in vitro (FIV) foram bisseccionados manualmente e segregados em hemi-zigotos enucleados (citoplastos FIV) e não enucleados (carioplastos FIV). Células de um cultivo celular estabelecido a partir da biópsia auricular de uma fêmea bovina adulta foram utilizadas como núcleos doadores (carioplasto CS). As estruturas foram dispostas em (a) grupos controle: FIV; partenogênese com oócitos com (PG c/) ou sem zona pelúcida (PG s/); e clone por TNCS; ou (b) grupos experimentais: G1, citoplasto FIV + citoplasto MII + carioplasto CS; G2, citoplasto MII + carioplasto FIV; G3, citoplasto FIV + carioplasto FIV; G4, citoplasto FIV + citoplasto FIV + carioplasto CS; e G5, citoplasto MII + carioplasto MII. Após a eletrofusão das estruturas, os grupos experimentais G1 a G45 foram divididos em subgrupos de AQ ou AE. O cultivo in vitro foi realizado pelo sistema WOW (well-of-the-well). Após 20 repetições, as taxas de clivagem (D2) e blastocisto (D7) foram comparadas pelos testes de χ2 e os valores para o número total de células e a alocação das linhagens celulares nos blastocistos, determinados por coloração diferencial, foram avaliados por análise de variância, com pareamento comparativo pelo teste de Tukey, para P<0,05. O único grupo experimental que apresentou desenvolvimento embrionário no D7 semelhante aos controles FIV (27,0%) e TNCS (31,4%) foi o subgrupo G1 AE (28,2%). Isso pode ser atribuído a uma melhor sincronia do ciclo celular entre citoplastos e/ou carioplasto e um mais adequado processo de ativação. O desenvolvimento embrionário nos grupos G1 AQ (13,7%), G4 AQ (6,4%) e G4 AE (8,7%) foi menor do que o G1 AE, possivelmente devido à assincronia do processo de ativação ou ciclo celular. O desenvolvimento embrionário nulo dos grupos G2 e G3, independente da ativação, possivelmente foi decorrente da manipulação das estruturas em um momento biologicamente sensível. Da mesma forma, a baixa clivagem (57,0%) e o desenvolvimento nulo no grupo G5 de ativação espontânea demonstraram de fato que a manipulação estimulou o processo de ativação embrionária de forma sub-limiar. Em geral, não houve diferença no número de células e alocação celular nos grupos onde houve desenvolvimento até o estádio de blastocisto. Conclui-se que o processo de ativação foi tão significativo para o desenvolvimento embrionário que o tipo de citoplasto e carioplasto usados na reconstrução embrionária. A produção de embriões clones com um método mais fisiológico de ativaçao (AE) mostrou-se como um procedimento viável, obtendo-se no grupo G1 AE a mesma eficiência observada na FIV ou na TNCS
Kremer, Natacha. "Évolution de la dépendance dans les symbioses à Wolbachia : étude du genre Asobara (Hymenoptera : braconidae)." Thesis, Lyon 1, 2009. http://www.theses.fr/2009LYO10141.
Full textAssociations between eukaryotes and micro-organisms are frequently observed in nature and range along the continuum between parasitism and mutualism. Numerous associations have already been well described; however the origin and the evolution of these associations are rarely studied. We focused on the intracellular bacterium Wolbachia, which induces very different phenotypic effects, ranging from facultative reproductive parasitism in Arthropods to obligatory mutualism in Nematodes. Here we studied the hymenopteran Asobara tabida, a rare species in which Wolbachia is necessary for oogenesis completion of its Arthropod host, in order to investigate the mechanisms underlying an evolutionarily recent transition. We first studied the variability of dependence to Wolbachia within the Asobara genus. Using various transcriptomic approaches, we next characterized molecular echanisms involved in dependence between A. tabida and Wolbachia, and highlighted processes implicated in programmed cell death, immunity (broad sense) and development. Finally, we examined to what extent Wolbachia impacts host physiology, by studying iron metabolism and global immunity in various symbiotic associations. These studies highlight that dependence is not always linked with the provision of a new function. It could rather reflect host compensatory mechanisms in response to physiological perturbations induced by the presence of symbiont. More generally, these results invite to consider the effects and the consequences of symbionts over the mechanisms allowing their persistence within populations
Hellemans, Simon. "Ecology and reproduction of neotropical soil-feeding termites from the Termes group." Doctoral thesis, Universite Libre de Bruxelles, 2019. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/286072.
Full textDoctorat en Sciences
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Defendini, Hélène. "Bases génétiques et conséquences évolutives de la perte de sexe dans le groupe des pucerons." Electronic Thesis or Diss., Rennes, Agrocampus Ouest, 2023. http://www.theses.fr/2023NSARA094.
Full textSexual reproduction is considered the ancestral reproductive mode of eukaryotes, yet it has been lost several times in many taxa. Understanding the mechanisms by which asexual lineages appear and persist over time remains a major challenge of evolutionary biology. During my PhD, I investigated the genetic basis as well as the evolutionary consequences of sex loss in aphids, a group that displays reproductive polymorphism. The ancestral reproductive mode of aphids is cyclical parthenogenesis (CP, an alternation of several parthenogenetic generations and one sexual generation), but obligate parthenogenesis (OP) is frequently observed in this group. Derived OP lineages are not able to produce sexual females though they often retain the ability to produce males. First, to characterize genomic regions involved in the transition from CP to OP reproductive mode, we used genome scan approaches on different aphid taxa that are more or less genetically related and exhibit variation in reproductive mode. We showed that the genetic basis of sex loss is different between the studied taxa, with no apparent convergence in gene content norfunctions. Thus, several independent genomic regions may be responsible for sex loss in aphids, suggesting that there are many paths that lead to asexuality in this group. Second, we studied the evolutionary consequences of the loss of sex on traits and genes essential for sexual reproduction. Since the males produced by OP lineages are unlikely to pass on their genes (because CP lineages are usually separated from OP ones), we tested the prediction that male traits should degenerate. Male production was indeed reduced in OP lineages, supposedly resulting from counter-selection, but male reproductive success was only slightly lower than in CP lineages, presumably due to the slow action of relaxed selection orunderestimation of reproductive opportunities. As OP lineages produce rare males and also do not produce sexual females, the gene expression of parthenogenetic females in these OP lineages is no longer constrained by that of other morphs. We thus predicted that the disappearance of sexual conflict (which arises when there are different morph-specific optima for a trait shared by different morphs) would result in shifts of gene expression. We therefore compared gene expression patterns of CP and OP lineages for different morphs in the pea aphid. We observed that gene expression in males from OP lineages tended towards the parthenogenetic female optimum, as predicted by theory. More surprisingly, males and parthenogenetic females of OP lineages consistently over-expressed genes typically expressed in the gonads of sexual morphs. These changes in gene expression in OP lineages may arise from the relaxation of selection or the repurposing of gene networks otherwise used in sexual lineages. This thesis illustrates the relevance of using species with polymorphic reproductive systems to understand the evolutionary history of sex loss and its consequences
Fisher, David Lockwood. "Comparative life history studies of sexual and parthenogenetic Liposcelis." Thesis, University of Reading, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.264839.
Full textPennarossa, G. "CENTROSOME BIOGENESIS AND ADAPTIVE RESPONSE IN MAMMAL PARTHENOGENETIC CELLS." Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/169555.
Full textAhmad, Ruhel [Verfasser], and Albrecht [Akademischer Betreuer] Müller. "Neurogenesis from parthenogenetic human embryonic stem cells / Ruhel Ahmad. Betreuer: Albrecht Müller." Würzburg : Universitätsbibliothek der Universität Würzburg, 2013. http://d-nb.info/1031379878/34.
Full textSamandar, eweis Dureen. "Asymmetric division in single cell nematode embryos outside the Caenorhabditis genus." Electronic Thesis or Diss., Université Paris sciences et lettres, 2021. http://www.theses.fr/2021UPSLS063.
Full textAsymmetric cell division is an essential process of development. The process and its regulation have been studied extensively in the Caenorhabditis elegans embryo. Asymmetric division of the single-cell embryo is a conserved process in nematode species, however, the cellular features leading up to division are surprisingly variable. During my PhD, I aimed to study these differences by using two non-C. elegans embryos: Diploscapter pachys and Pristionchus pacificus. D. pachys is the closest parthenogenetic relative to C. elegans. Since the polarity cue in C. elegans is brought by the sperm, how polarity is triggered in D. pachys remains unknown. My results show that the nucleus inhabits principally the hemisphere of the D. pachys embryo that will become the posterior pole. Moreover, in embryos where the nucleus is forced to one pole by centrifugation, it returns to its preferred pole. Although the embryo is polarized, cortical ruffling and actin cytoskeleton at both poles appear identical. Interestingly, the location of the meiotic spindle also correlates with the future posterior cell. In some oocytes, a slight actin enrichment along with unusual microtubule structures emanating from the meiotic spindle are observed at the future posterior pole. Overall, my main PhD project shows that polarity of the D. pachys embryo is attained during meiosis wherein the meiotic spindle could potentially be playing a role by a mechanism that may be present but suppressed in C. elegans. For P. pacificus, biolistic transgenesis has been shown recently successful. However, due to a lack of a stringent selection marker, the continuation of this project was unfeasible during my PhD. Altogether, the results of my PhD add to the understanding of non-C. elegans early embryogenesis and emphasizes on the importance of using these species for comparative studies
Sukumaran, Sandhya. "Genotoxic responses and population level effects of mutagen exposure in bisexual and parthenogenetic Artemia." Thesis, University of East Anglia, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.551144.
Full textKnebelsberger, Thomas. "Geographische Parthenogenese bei der Schabe Phyllodromica subaptera (Blattoptera, Blattellidae, Ectobiinae) und Revision des subaptera-Artenkomplexes." Diss., kostenfrei, 2008. http://edoc.ub.uni-muenchen.de/8966/.
Full textReichel, Katja. "Effets de la reproduction partiellement asexuée sur la dynamique des fréquences génotypiques en populations majoritairement diploïdes." Thesis, Rennes, Agrocampus Ouest, 2015. http://www.theses.fr/2015NSARC123/document.
Full textReproductive systems determine how genetic material is passed from one generation to the next, making them an important factor for evolution. Organisms that combine sexual and asexual/clonal reproduction are very widespread [… yet] the effects of their reproductive system on their evolution are still controversial and poorly understood.The aim of this thesis was to model the dynamics of genotype frequencies under combined sexual/clonal reproduction in dominantly diploid life cycles [. … A] state and time discrete Markov chain model served as the mathematical basis to describe [their] changes […] through time.The results demonstrate that partial clonality may indeed change the dynamics of genomic diversity compared to either exclusively sexual or exclusively clonal populations. […] Time has a crucial role in partially clonal populations and needs to be taken into account in any analysis of their genomic diversity.This thesis provides recommendations for data collection and a null hypothesis for the interpretation of population genetic/genomic data […]. Moreover, it includes new methods for the analysis of genotype-based population genetic Markov chain models. These results have a high potential relevance in several areas, ranging from basic research […] to applications in agriculture […], fisheries […] and nature conservation […]
Rosenberger, Martin Julien [Verfasser], Stefan [Akademischer Betreuer] Scheu, Mark [Akademischer Betreuer] Maraun, and Ulrich [Akademischer Betreuer] Brose. "Phylogeography in sexual and parthenogenetic European oribatida / Martin Julien Rosenberger. Gutachter: Stefan Scheu ; Mark Maraun ; Ulrich Brose. Betreuer: Stefan Scheu." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2011. http://d-nb.info/1043612831/34.
Full textWinger, Quinton A. "Expression of insulin-like growth factors (IGF) and their binding proteins (BP) in fertilized and parthenogenetic bovine embryos, regulators of early development." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq21055.pdf.
Full textBergmann, Paavo Karl [Verfasser], and Michael [Akademischer Betreuer] Heethoff. "Development and function of the genital organs in the parthenogenetic oribatid mite Archegozetes longisetosus Aoki 1965 / Paavo Karl Bergmann ; Betreuer: Michael Heethoff." Tübingen : Universitätsbibliothek Tübingen, 2015. http://d-nb.info/1163397261/34.
Full textCoutinho, Ana Rita Sousa. "Presença da Caspase-3 ativa e das proteínas de reparo de lesões do DNA em embriões suínos ativados partenogeneticamente com alta ou baixa capacidade de desenvolvimento." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/10/10131/tde-12122007-100619/.
Full textApoptosis is a highly conserved form of cell death that plays a major role in animal development and cellular homeostasis by acting as a quality control mechanism to remove cells that are damaged, nonfunctional, misplaced or supranumerary. This form of cell death plays a major role on preimplantation embryonic development since embryonic cells are often subject to DNA damage, triggering either DNA damage and repair mechanisms or apoptosis. Once initiated the apoptotic process leads to caspase activation and cleavage of cellular substrates. The aim of the present study was to quantify active Caspase-3 (+casp-3) and to determine the role of this pro-apoptotic enzyme on the development of preimplantation porcine embryos, as well as to investigate the presence and localization of DNA damage and repair proteins. Four experiments were conducted using slaughterhouse immature oocytes collected from pre-pubertal gilt ovaries and in vitro matured (IVM) for 44-46 h. Metaphase II (MII) oocytes were parthenogenetically activated (PA) using ionomycin and strontium chloride and cultured in PZM-3 at 38ºC, 5% CO2 in air and high humidity. In the first study embryos were distributed into 4 groups according to cleavage time and cell number: R4 - cleaved at 24 h with ≥4-cells at 48 h; R2 - cleaved at 24 h with 2-3 cells at 48 h; L4 - non-cleaved at 24 h with ≥4-cells at 48 h; L2 - non-cleaved at 24 h with 2-3 cells at 48 h. Group R embryos showed higher blastocyst rates R4-66.1 (174/263) and R2-59.6 (62/104) and more nuclei per blastocyst, R4-40.1 and R2-38.9, when compared to group L L4-15.4 (6/39) and L2-16.8 (13/77); L4-18.5 and L2-18.3 (Chi-square and Tukey-Kramer, P<0.05); however, there were no differences between R4 and R2 or L4 and L2. The second experiment used only early-(R) and late-cleaved embryos (L), classified at 24 h of IVC, fixed at D-2, D-4 and D-6 and then stained for +casp-3 immunofluorescence. In this embryos fixed at D-2, D-4 and D-6 were considered as sub-experiments conducted in different replicates. Active Caspase-3 cytoplasmic signal was detected in cultured embryos from D2 to D6 and nuclear signal was detected from D5 to D6. The relative amount of immunofluorescence signal for +casp-3 for groups R and L at D2, D4 and D6 of culture was 2.4 vs. 1.4; 1.1 vs. 1.0 and 1.1 vs. 1.2, respectively. A third experiment was conducted to evaluate the role of +casp-3 on porcine preimplantation embryos. In this study the Caspase inhibitor Z-DEVD-fmk (100 uM) was supplemented during maturation of porcine oocytes or embryo culture (D0 to D2 or D4 to D6). Addition of the caspase inhibitor during IVM or D4 to D6 of culture did not affect blastocyst rate. However, caspase inhibition from D0 to D2 increased development of porcine embryos to the blastocyst stage [55.1 (59/107) and 37.5 (39/104) for control and Z-DEVD-fmk, respectively; Chi-square, P<0.05). The last experiment investigated the presence of DNA damage and repair proteins γH2AX, 52BP1, NSB1, and Rad52 in early- and late-cleaved embryos by immunofluorescence. There was no 53BP1 signal in PA porcine embryos at beginning of IVC. Late-cleaved embryos showed higher γH2AX signal than early-cleaved embryos; however, there was no difference between NSB1 and Rad52 staining between these embryos. In conclusion, apoptosis and DNA damage and repair mechanisms play a role on development of porcine embryos. Active caspase-3 is present in porcine embryos throughout the preimplantation period and inhibition of this enzyme at early stages of in vitro culture can increase blastocyst rate of PA embryos. Moreover, late-cleaved embryos carry higher DNA damage than early-cleaved embryos. Therefore, the relationship between DNA repair mechanism and developmental potential of porcine embryos need to be further investigated.