Gotowe bibliografie tematyczne / Petunia Reproduction

Gotowa bibliografia na temat „Petunia Reproduction”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 30 stycznia 2023

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Artykuły w czasopismach na temat "Petunia Reproduction"

Clark, David G., Chris Dervinis, Francine Cuquel, Harry Klee, Jim Barrett i Terril Nell. "469 Multi-faceted Approaches to Genetic Engineering of Petunia × hybrida for Delayed Leaf Senescence". HortScience 35, nr 3 (czerwiec 2000): 474F—475. http://dx.doi.org/10.21273/hortsci.35.3.474f.

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In an effort to modify and study leaf senescence, we have produced several different transgenic petunia lines with altered leaf senescence phenotypes. Using two promoters from senescence-associated genes (sag12 & sag13) fused to the isopentenyl transferase (IPT) gene, which catalyzes the rate-limiting step of cytokinin production, we have produced transgenic petunia plants with delayed lower leaf senescence. We have observed that apparent “leaky” expression of IPT gives rise to plants with other morphological alterations such as increased branching habit and decreased root formation. Plants with delayed leaf senescence phenotypes were selected and bred to produce progeny that were evaluated in greenhouse experiments. Breeding characteristics, horticultural performance and reproduction of these plants will be discussed in terms of potential commercial benefits and limitations. Using the sag12 promoter to drive expression of the knotted (KN1) gene, we have also been able to engineer petunia plants with delayed lower leaf senescence. Initial progeny evaluations of sag12-KN1 petunias will also be discussed.

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Gubrium, E. K., D. G. Clark, H. J. Klee, T. A. Nell i J. E. Barrett. "Analysis of Horticultural Performance of Ethylene-insensitive Petunias and Tomatoes". HortScience 32, nr 3 (czerwiec 1997): 499D—499. http://dx.doi.org/10.21273/hortsci.32.3.499d.

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We are studying the horticultural performance of two model plant systems that carry a mutant gene that confers ethylene-insensitivity: Never Ripe tomatoes and petunia plants transformed with the mutant etr1-1 gene isolated from Arabidopsis thaliana. Having two model systems to compare side-by-side allows us to determine with greater certainty ethylene's role at different developmental stages. Presence of the mutant etr1-1 gene in transgenic petunias was determined using three techniques: PCR analysis, the seedling triple response assay (inhibition of stem elongation, radial swelling of stem and roots, and an exaggerated apical hook when grown in the dark and in the presence of ethylene), and the flower wilting response to pollination, which is known to be induced by ethylene. Flowers from ethylene-insensitive petunias took almost four times as long to wilt after pollination as wild-type plants. It is well known that fruit ripening in Never Ripe tomato is inhibited, and a similar delayed fruit ripening phenotype is observed in petunia plants transformed with etr1-1. In an effort to maintain ethylene-insensitive petunia plants by vegetative propagation, we observed that the rate of adventitious root formation was much lower with transgenic plants than in wild-type plants. In subsequent experiments on adventitious root formation in Never Ripe tomato, we observed the same result. Therefore, while ethylene-insensitive tomato and petunia plants appear phenotypically normal for many characters, other factors are altered by the presence of this mutation. The fact that these changes are present in two model systems helps to define the role of ethylene perception in plant growth and reproduction.

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Gubrium, Erika K., Donna J. Clevenger, David G. Clark, James E. Barrett i Terril A. Nell. "Reproduction and Horticultural Performance of Transgenic Ethylene-insensitive Petunias". Journal of the American Society for Horticultural Science 125, nr 3 (maj 2000): 277–81. http://dx.doi.org/10.21273/jashs.125.3.277.

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A series of experiments on ethylene-insensitive (EI) petunia plants (Petunia ×hybrida Hort. Vilm.-Andr.) generated in two genetic backgrounds were conducted to determine the involvement of ethylene in horticultural performance. Experiments examined various aspects of horticultural performance: days to flower, flower senescence after pollination and without pollination, fruit set and ripening, and adventitious root formation on vegetative stem cuttings. The development of EI plants was altered in several ways. Time from seed sowing to first flower anthesis was decreased by a week for EI plants grown at 26/21 °C. Flower senescence in nonpollinated and self-pollinated flowers was delayed in all EI plants compared to wild-type plants. Fruit set percentage on EI plants was slightly lower than on wild-type plants and fruit ripening on EI plants was delayed by up to 7 days. EI plants produced fewer commercially acceptable rooted cuttings than wild-type plants. There was a basic difference in the horticultural performance of the two EI lines examined due to a difference in the genetic backgrounds used to generate the lines. EI plants displayed better horticultural performance when grown with day/night temperatures of 26/21 °C than 30/24 °C. These results suggest that tissue-specific ethylene insensitivity as well as careful consideration of the genetic background used in transformation procedures and growth conditions of etr1-1 plants will be required to produce commercially viable transgenic floriculture crops. EI petunias provide an ideal model system for studying the role of ethylene in regulating various aspects of plant reproduction.

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Liu, H. Y., J. L. Sears, M. Bandla, A. M. Harness i B. Kulemeka. "First Report of Calibrachoa mottle virus Infecting Petunia". Plant Disease 87, nr 12 (grudzień 2003): 1538. http://dx.doi.org/10.1094/pdis.2003.87.12.1538a.

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Calibrachoa mottle virus (CbMV), a tentative carmovirus, was first isolated and reported by Liu et al. (1) from infected Calibrachoa plants. During the spring of 2003, petunia samples from Florida and California sent to testing services at Agdia, Inc (Elkhart IN) tested positive for CbMV by enzyme-linked immunosorbent assay (ELISA) and lateral flow immunoassay (ImmunoStrips). These samples also tested positive by carmovirus group-specific polymerase chain reaction (PCR) primers and by immunocapture PCR (2). RNA extracted from these samples with the RNeasy Plant Kit (Qiagen Inc., Valencia, CA) hybridized with a digoxigenin labeled probe derived from purified CbMV viral RNA. All plant samples that tested positive for CbMV were symptomless except one symptomatic sample that also tested positive for Tobacco mosaic virus. From samples that tested positive for CbMV only, mechanical inoculations were made to Chenopodium quinoa at a USDA-ARS greenhouse in Salinas, CA. Representative single, local lesions were used to inoculate additional C. quinoa plants. The resulting local lesions from these inoculations were freeze-dried and further used as virus inoculum (CbMV petunia). Similar inoculum was made with CbMV isolated from Calibrachoa plants (CbMV calibrachoa). Virus-free Petunia hybrida cultivars Surfinia ‘Baby Pink’ and Surfinia ‘Violet’ (Jackson and Perkins Inc., Somis, CA) were mechanically inoculated with CbMV petunia and CbMV calibrachoa. Four weeks postinoculation, all plants were tested using ELISA for the presence of CbMV. In greenhouse conditions, 14.3% of ‘Baby Pink’ plants were positive for CbMV petunia, whereas none were positive for CbMV calibrachoa. ‘Violet’ plants were 64.3 and 33.3% positive for CbMV petunia and CbMV calibrachoa, respectively. None of the positive plants expressed virus-like symptoms. Virus particles resembling those of CbMV were observed from infected petunia plants with transmission electron microscopy in leaf-dip preparations. To our knowledge, this is the first report of CbMV infecting petunia. Commercial reproduction of petunia plants and maintenance of genetic mother stock are usually by vegetative propagation. CbMV can be transmitted mechanically and is readily propagated along with its host. To produce healthy petunia plants, virus-free mother stock should be used, which requires regular screening of mother stock for CbMV. Reference: (1) H.-Y. Liu et al. Plant Dis. 87:167, 2003. (2) A. M. Harness et al. (Abstr.) Phytopathology 92:S34, 2002.

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Adebesin, Funmilayo, Joshua R. Widhalm, Benoît Boachon, François Lefèvre, Baptiste Pierman, Joseph H. Lynch, Iftekhar Alam i in. "Emission of volatile organic compounds from petunia flowers is facilitated by an ABC transporter". Science 356, nr 6345 (29.06.2017): 1386–88. http://dx.doi.org/10.1126/science.aan0826.

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Plants synthesize a diversity of volatile molecules that are important for reproduction and defense, serve as practical products for humans, and influence atmospheric chemistry and climate. Despite progress in deciphering plant volatile biosynthesis, their release from the cell has been poorly understood. The default assumption has been that volatiles passively diffuse out of cells. By characterization of aPetunia hybridaadenosine triphosphate–binding cassette (ABC) transporter, PhABCG1, we demonstrate that passage of volatiles across the plasma membrane relies on active transport.PhABCG1down-regulation by RNA interference results in decreased emission of volatiles, which accumulate to toxic levels in the plasma membrane. This study provides direct proof of a biologically mediated mechanism of volatile emission.

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Iftikhar, Junaid, Meiling Lyu, Zhuoyi Liu, Nasir Mehmood, Nigarish Munir, Mohamed A. A. Ahmed, Wajjiha Batool, Mehtab Muhammad Aslam, Yuan Yuan i Binghua Wu. "Sugar and Hormone Dynamics and the Expression Profiles of SUT/SUC and SWEET Sugar Transporters during Flower Development in Petunia axillaris". Plants 9, nr 12 (14.12.2020): 1770. http://dx.doi.org/10.3390/plants9121770.

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Flowering is the first committed step of plant sexual reproduction. While the developing flower is a strong sink requiring large quantity of sugars from photosynthetic source tissues, this process is under-temper-spatially controlled via hormone signaling pathway and nutrient availability. Sugar transporters SUT/SUC and SWEET mediate sugars movement across membranes and play a significant role in various physiological processes, including reproductive organ development. In Petunia axillaris, a model ornamental plant, 5 SUT/SUC and 36 SWEET genes are identified in the current version of the genome. Analysis of their gene structure and chromosomal locations reveal that SWEET family is moderately expanded. Most of the transporter genes are abundantly expressed in the flower than in other organs. During the five flower developmental stages, transcript levels of PaSUT1, PaSUT3, PaSWEET13c, PaSWEET9a, PaSWEET1d, PaSWEET5a and PaSWEET14a increase with the maturation of the flower and reach their maximum in the fully open flowers. PaSWEET9c, the nectar-specific PhNEC1 orthologous, is expressed in matured and fully opened flowers. Moreover, determination of sugar concentrations and phytohormone dynamics in flowers at the five developmental stages shows that glucose is the predominant form of sugar in young flowers at the early stage but depletes at the later stage, whereas sucrose accumulates only in maturated flowers prior to the corolla opening. On the other hand, GA3 content and to a less extent IAA and zeatin decreases with the flower development; however, JA, SA and ABA display a remarkable peak at mid- or later flower developmental stage.

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Jankovics, T., Y. Bai, G. M. Kovács, M. Bardin, P. C. Nicot, H. Toyoda, Y. Matsuda, R. E. Niks i L. Kiss. "Oidium neolycopersici: Intraspecific Variability Inferred from Amplified Fragment Length Polymorphism Analysis and Relationship with Closely Related Powdery Mildew Fungi Infecting Various Plant Species". Phytopathology® 98, nr 5 (maj 2008): 529–40. http://dx.doi.org/10.1094/phyto-98-5-0529.

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Previous works indicated a considerable variation in the pathogenicity, virulence, and host range of Oidium neolycopersici isolates causing tomato powdery mildew epidemics in many parts of the world. In this study, rDNA internal transcribed spacer (ITS) sequences, and amplified fragment length polymorphism (AFLP) patterns were analyzed in 17 O. neolycopersici samples collected in Europe, North America, and Japan, including those which overcame some of the tomato major resistance genes. The ITS sequences were identical in all 10 samples tested and were also identical to ITS sequences of eight previously studied O. neolycopersici specimens. The AFLP analysis revealed a high genetic diversity in O. neolycopersici and indicated that all 17 samples represented different genotypes. This might suggest the existence of either a yet unrevealed sexual reproduction or other genetic mechanisms that maintain a high genetic variability in O. neolycopersici. No clear correlation was found between the virulence and the AFLP patterns of the O. neolycopersici isolates studied. The relationship between O. neolycopersici and powdery mildew anamorphs infecting Aquilegia vulgaris, Chelidonium majus, Passiflora caerulea, and Sedum alboroseum was also investigated. These anamorphs are morphologically indistinguishable from and phylogenetically closely related to O. neolycopersici. The cross-inoculation tests and the analyses of ITS sequences and AFLP patterns jointly indicated that the powdery mildew anamorphs collected from the above mentioned plant species all represent distinct, but closely related species according to the phylogenetic species recognition. All these species were pathogenic only to their original host plant species, except O. neolycopersici which infected S. alboroseum, tobacco, petunia, and Arabidopsis thaliana, in addition to tomato, in cross-inoculation tests. This is the first genome-wide study that investigates the relationships among powdery mildews that are closely related based on ITS sequences and morphology. The results indicate that morphologically indistinguishable powdery mildews that differed in only one to five single nucleotide positions in their ITS region are to be considered as different taxa with distinct host ranges.

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Immink, R. G., D. J. Hannapel, S. Ferrario, M. Busscher, J. Franken, M. M. Lookeren Campagne i G. C. Angenent. "A petunia MADS box gene involved in the transition from vegetative to reproductive development". Development 126, nr 22 (15.11.1999): 5117–26. http://dx.doi.org/10.1242/dev.126.22.5117.

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We have identified a novel petunia MADS box gene, PETUNIA FLOWERING GENE (PFG), which is involved in the transition from vegetative to reproductive development. PFG is expressed in the entire plant except stamens, roots and seedlings. Highest expression levels of PFG are found in vegetative and inflorescence meristems. Inhibition of PFG expression in transgenic plants, using a cosuppression strategy, resulted in a unique nonflowering phenotype. Homozygous pfg cosuppression plants are blocked in the formation of inflorescences and maintain vegetative growth. In these mutants, the expression of both PFG and the MADS box gene FLORAL BINDING PROTEIN26 (FBP26), the putative petunia homolog of SQUAMOSA from Antirrhinum, are down-regulated. In hemizygous pfg cosuppression plants initially a few flowers are formed, after which the meristem reverts to the vegetative phase. This reverted phenotype suggests that PFG, besides being required for floral transition, is also required to maintain the reproductive identity after this transition. The position of PFG in the hierarchy of genes controlling floral meristem development was investigated using a double mutant of the floral meristem identity mutant aberrant leaf and flower (alf) and the pfg cosuppression mutant. This analysis revealed that the pfg cosuppression phenotype is epistatic to the alf mutant phenotype, indicating that PFG acts early in the transition to flowering. These results suggest that the petunia MADS box gene, PFG, functions as an inflorescence meristem identity gene required for the transition of the vegetative shoot apex to the reproductive phase and the maintenance of reproductive identity.

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Wittmann, D., R. Radtke, J. R. Cure i M. T. Schifino-Wittmann. "Coevolved reproductive strategies in the oligolectic bee Callonychium petuniae (Apoidea, Andrenidae) and three purple flowered Petunia species (Solanaceae) in southern Brazil". Journal of Zoological Systematics and Evolutionary Research 28, nr 3 (27.04.2009): 157–65. http://dx.doi.org/10.1111/j.1439-0469.1990.tb00373.x.

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Callaway, Tara D., i Anu Singh-Cundy. "HD-AGPs as Speciation Genes: Positive Selection on a Proline-Rich Domain in Non-Hybridizing Species of Petunia, Solanum, and Nicotiana". Plants 8, nr 7 (8.07.2019): 211. http://dx.doi.org/10.3390/plants8070211.

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Transmitting tissue-specific proteins (TTS proteins) are abundant in the extracellular matrix of Nicotiana pistils, and vital for optimal pollen tube growth and seed set. We have identified orthologs from several species in the Solanaceae, including Petunia axillaris axillaris and Petunia integrifolia. We refer to TTS proteins and their orthologs as histidine domain-arabinogalactan proteins (HD-APGs). HD-AGPs have distinctive domains, including a small histidine-rich region and a C-terminal PAC domain. Pairwise comparisons between HD-AGPs of 15 species belonging to Petunia, Nicotiana, and Solanum show that the his-domain and PAC domain are under purifying selection. In contrast, a proline-rich domain (HV2) is conserved among cross-hybridizing species, but variant in species-pairs that are reproductively isolated by post-pollination pre-fertilization reproductive barriers. In particular, variation in a tetrapeptide motif (XKPP) is systematically correlated with the presence of an interspecific reproductive barrier. Ka/Ks ratios are not informative at the infrageneric level, but the ratios reveal a clear signature of positive selection on two hypervariable domains (HV1 and HV2) when HD-AGPs from five solanaceous genera are compared. We propose that sequence divergence in the hypervariable domains of HD-AGPs reinforces sympatric speciation in incipient species that may have first diverged as a consequence of pollinator preferences or other ecological factors.

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Rozprawy doktorskie na temat "Petunia Reproduction"

Tan, Lor-Wai. "Biochemical aspects of self-incompatibility in Petunia hybrida". Title page, Contents and Summary only, 1988. http://web4.library.adelaide.edu.au/theses/09A/09at161.pdf.

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YeYing, Wang Ying. "Occurrence and Charactrisation of Superoxide Dismutases in the Female Reproductive Structures of Petunia". Thesis, University of Canterbury. Biological Sciences, 2006. http://hdl.handle.net/10092/1341.

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Superoxide Dismutase (SOD) activity in cell-free extracts prepared from healthy mature flowers of Petunia hybrida (variety 'Hurrah') was studied. The SOD activity in the crude extracts was stable for more than one month when stored at -20 oC. It was found that pH 7.8 is optimal for SOD activity. Different flower tissues of petunia (stigma, style and ovary) at various stages of development were extracted and analysed for SOD activity. SOD activity was found to be significantly highest in the ovary tissue of dehiscent petunia flowers. Three SOD isozymes were detected after crude extracts of the different female reproductive tissues of petunia flowers were analysed on a non-denaturing polyacrylamide gel electrophoresis system. Based on a difference in the sensitivity of the SOD isoforms to H2O2 and KCN, it is suggested that Mn-SOD, Fe-SOD and Cu/Zn-SOD were present in the crude extracts of the female reproductive tissues of petunia flowers. The response of the female reproductive parts of petunia flowers was also tested under water deficiency and high temperature (35 oC) stress. The SOD activity seemed to increase more in response to the high temperature than the water deficiency stress. Intense blue staining was observed from developing younger buds, and much lower formazan deposition was detected at the later stage. This indicates the lower O2- produced during later stages mainly due to increasing SOD synthesis. DEAE cellulose chromatography was successfully used to partially purify SOD from the ovaries of petunia flowers. The characteristics of the partially purified enzyme fraction were found to be very similar to those of the crude extracts.

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Moon, Bok Hee. "A study of the activity and characteristics of superoxide dismutase in the male reproductive parts of Petunia : a thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Plant Biotechnology in the School of Biological Sciences, University of Canterbury /". Thesis, University of Canterbury. Biological Sciences, 2006. http://hdl.handle.net/10092/1326.

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In the stamen (male reproductive tissue) of petunia 'Hurrah' flowers, the occurrence of SOD (superoxide dismutase) provided an effective anti-oxidative mechanism against superoxide production. Superoxide production and SOD activities at five developmental stages showed a positive correlation. The highest superoxide production and SOD activity in different parts of the stamen (anther, filament and pollen) were at stages with high metabolic activity: (i) during growing buds (in anthers and filaments) (ii) when flowers with predehiscent anthers were fully open (in pollen). In all parts of the stamen, SOD activity was the lowest at stage five (fully open flowers with dehiscent anthers), superoxide production was also lower at this stage with the exception of the pollen. The highest SOD activity was localized in anthers with the pollen, suggesting that the filaments only have a structural support function. SOD was examined on a native PAGE with regard to the isozymes present within the stamen of five developmental stages. Three isozymes, which were identified as Mn SOD, Fe SOD and Cu/Zn SOD by reactions with inhibitors, were commonly found at five developmental stages in crude extracts of anthers, filaments and pollen. The developmental stages with stronger isozyme bands on the native PAGE were consistent with the stages with higher SOD activities, and the Mn SOD and Fe SOD isozyme bands were more intense than Cu/Zn SOD bands, suggesting the activities of Mn SOD and Fe SOD in the crude extracts were much higher than Cu/Zn SOD. SOD from 1,000 stamens of dehiscent mature flowers was partially purified using ammonium sulphate fractionation and DEAE cellulose column chromatography. The purified bound fraction contained only one SOD isozyme on a native PAGE, which was shown to be a Mn SOD, as it is sensitive to neither hydrogen peroxide nor cyanide. The specific activity of the purified SOD was 66.5 U/mg and the yield of total activity was 3.0%. The progress of enzyme purification was monitored using SDS-PAGE and the bound fraction contained two major polypeptide bands. The purified enzyme activity was optimal in the range of neutral pH, but it was the highest at pH 7.8. Through incubation at various pH levels for 24 hours, favourable stability of the purified fraction was confirmed around a pH range of 7 to 8.5. The purified enzyme retained 87% of its initial activity at -20 ? after one month of storage, but at 4 ? only 38% of the initial activity remained after the same period of storage.

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Tan, Lor-Wai. "Biochemical aspects of self-incompatibility in Petunia hybrida". Thesis, 1988. http://hdl.handle.net/2440/110363.

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Wang, Ye Ying. "Occurrence and charactrisation [i.e. characterization] of superoxide dismutases in the female reproductive structures of Petunia : a thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Plant Biotechnology in the University of Canterbury /". 2006. http://library.canterbury.ac.nz/etd/adt-NZCU20070117.142330.

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Części książek na temat "Petunia Reproduction"

Jackson, J. F. "DNA Repair in Petunia hybrida Pollen". W Sexual Reproduction in Higher Plants, 81–86. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73271-3_13.

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Vallade, Jean. "Quantitative Data on Petunia Embryogenesis: Mitotic Activity and Characteristics of the Cell Cycles". W Sexual Reproduction in Higher Plants, 389–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73271-3_62.

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Sun, Penglin, Justin Stephen Williams, Shu Li i Teh-hui Kao. "S-RNase-Based Self-Incompatibility in Petunia: A Complex Non-Self Recognition System Between Pollen and Pistil". W Sexual Reproduction in Animals and Plants, 289–303. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54589-7_24.

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Van Tunen, A. J., M. Busscher, L. Columbo, J. Franken i G. C. Angenent. "Molecular control of floral organogenesis and plant reproduction in Petunia hybrida". W Molecular and Cellular Aspects of Plant Reproduction, 9–16. Cambridge University Press, 1994. http://dx.doi.org/10.1017/cbo9780511752339.002.

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Ferrant, V., J. Van Went i M. Kries. "Ovule cDNA clones of Petunia hybrida encoding proteins homologous to MAP and shaggy/zeste-white 3 protein kinases". W Molecular and Cellular Aspects of Plant Reproduction, 159–72. Cambridge University Press, 1994. http://dx.doi.org/10.1017/cbo9780511752339.009.

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