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Artículos de revistas sobre el tema "Mus domesticus"

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Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 7 de febrero de 2022

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1

Baptista, Luciane Pansardi Cabreira. "Variabilidade na produção de embriões Mus domesticus domesticus". Acta Scientiae Veterinariae 32, n.º 3 (27 de junio de 2018): 253. http://dx.doi.org/10.22456/1679-9216.16909.

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2

Forejt, Jiří, Soňa Gregorová y Petr Jansa. "Three new t-haplotypes of Mus musculus reveal structural similarities to t-haplotypes of Mus domesticus". Genetical Research 51, n.º 2 (abril de 1988): 111–19. http://dx.doi.org/10.1017/s0016672300024125.

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SummaryThree new t-haplotypes, tp 4, tp 12 and tp 14, were isolated from M. musculus male mice captured in Central and East Bohemia, Czechoslovakia, about 400 km from the zone of hybridization between M. musculus and M. domesticus species. Complementation tests have shown that all three new t-haplotypes belong to tw 73 group. When compared with 5 t-haplotypes from M. domesticus they displayed the same pattern of BamHI restriction fragments with H-2 class I genes, and they also shared the t-specific 5·2 kb TaqI fragment of the alpha globin pseudogene. However, they differed from M. domesticus t-haplotypes at the D17Leh443 locus since they all displayed a 10·5 kb MspI fragment, labelled by the Tu443 probe, not found in wild type-chromosomes or in M. domesticus t-haplotypes. A hypothesis is proposed that t-haplotypes in M. domesticus originated by a single successful introgression from a parental species during speciation.

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3

Greene-Till, Rhonda, Yingping Zhao y Stephen C. Hardies. "Gene flow of unique sequences between Mus musculus domesticus and Mus spretus". Mammalian Genome 11, n.º 3 (marzo de 2000): 225–30. http://dx.doi.org/10.1007/s003350010041.

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4

Narayanswami, Sandya, Norman A. Doggett, Lynn M. Clark, Carl E. Hildebrand, Heinz-Ulrich Weier y Barbara A. Hamkalo. "Cytological and molecular characterization of centromeres in Mus domesticus and Mus spretus". Mammalian Genome 2, n.º 3 (1992): 186–94. http://dx.doi.org/10.1007/bf00302876.

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5

Zhao, Yingping, Lorrie P. Daggett y Stephen C. Hardies. "Mus spretus LINE-1s in the Mus musculus domesticus Inbred Strain C57BL/6J Are From Two Different Mus spretus LINE-1 Subfamilies". Genetics 142, n.º 2 (1 de febrero de 1996): 549–55. http://dx.doi.org/10.1093/genetics/142.2.549.

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Abstract A LINE-1 element, L1C105, was found in the Mus musculus domesticus inbred strain, C57BL/6J. Upon sequencing, this element was found to belong to a M. spretus LINE-1 subfamily originating within the last 0.2 million years. This is the second spretus-specific LINE-1 subfamily found to be represented in C57BL/6J. Although it is unclear how these M. spretus LINE-1s transferred from M. spretus to M. m. domesticus, it is now clear that at least two different spretus LINE-1 sequences have recently transferred. The limited divergence between the C57BL/6J spretus-like LINE-1s and their closest spretus ancestors suggests that the transfer did not involve an exceptionally long lineage of sequential transpositions.

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6

Dubin, R. A. "Functional comparison of the Mus musculus molossinus and Mus musculus domesticus Sry genes". Molecular Endocrinology 9, n.º 12 (1 de diciembre de 1995): 1645–54. http://dx.doi.org/10.1210/me.9.12.1645.

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7

Dubin, R. A., P. Coward, Y. F. Lau y H. Ostrer. "Functional comparison of the Mus musculus molossinus and Mus musculus domesticus Sry genes." Molecular Endocrinology 9, n.º 12 (diciembre de 1995): 1645–54. http://dx.doi.org/10.1210/mend.9.12.8614401.

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8

Bustos-Obregón, Eduardo y Christopher Olivares. "Boron as Testicular Toxicant in Mice (Mus domesticus)". International Journal of Morphology 30, n.º 3 (septiembre de 2012): 1106–14. http://dx.doi.org/10.4067/s0717-95022012000300057.

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9

Nishioka, Yutaka. "Two types of mouse (Mus musculus domesticus) Y chromosomes in Quebec". Genome 35, n.º 3 (1 de junio de 1992): 534–37. http://dx.doi.org/10.1139/g92-078.

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A Y chromosomal repetitive sequence identified two types of Y chromosomes in mice (Mus musculus domesticus) caught near Ste. Anne de Bellevue, Quebec. One type is apparently identical to the Y chromosome found in Maryland, Delaware, and California, whereas the other type is similar, but not identical, to the Y chromosome present in M.m. poschiavinus, an Alpine race of M.m. domesticus. These findings suggest that the domesticus Y chromosome is highly polymorphic and thus useful for elucidating the relationships among American and European house mouse populations.Key words: mouse Y chromosome, polymorphism, Mus musculus domesticus, repetitive sequence, Quebec.

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10

Orth, Annie, Theophilus Adama, Waheedud Din y François Bonhomme. "Hybridation naturelle entre deux sous-espèces de souris domestique, Mus musculus domesticus et Mus musculus castaneus, près du lac Casitas (Californie)". Genome 41, n.º 1 (1 de febrero de 1998): 104–10. http://dx.doi.org/10.1139/g97-109.

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The house mouse Mus musculus is a polytypic species, distributed worldwide, with three main subspecies: M. m. musculus in the North-East of Eurasia, M. m. castaneus in South-East Asia, and M. m. domesticus in Europe, the Near-East, and Africa. This last subspecies may also be found in Australia and the Americas, where it was brought by European colonization. Previous studies, however, have shown the presence of specific antiviral determinants of Asian origin in a mouse population at Lake Casitas, California. In this study, an analysis of the variability at 35 enzyme loci demonstrates the hybrid nature of this Californian population intermediate between M. m. castaneus and M. m. musculus. Restriction fragment length polymorphisms of two fragments of the mitochondrial DNA also confirm unambiguously the presence of two types of matrilines in comparable frequencies in our sample. Nevertheless, the study of a subspecies-specific Y chromosome microdeletion in the Zfy2 gene reveals only theM. m. domesticus haplotype at Lake Casitas, a phenomenon comparable with the one observed in other hybrid zones of the M. musculus complex. These findings testify once more that genetic exchanges between subspecies inside the broader M. musculus gene pool are still possible.

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11

Searle, Jeremy B., Paul M. Jamieson, İslam Gündüz, Mark I. Stevens, Eleanor P. Jones, Chrissen E. C. Gemmill y Carolyn M. King. "The diverse origins of New Zealand house mice". Proceedings of the Royal Society B: Biological Sciences 276, n.º 1655 (30 de septiembre de 2008): 209–17. http://dx.doi.org/10.1098/rspb.2008.0959.

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Molecular markers and morphological characters can help infer the colonization history of organisms. A combination of mitochondrial (mt) d -loop DNA sequences, nuclear DNA data, external measurements and skull characteristics shows that house mice ( Mus musculus ) in New Zealand and its outlying islands are descended from very diverse sources. The predominant genome is Mus musculus domesticus (from western Europe), but Mus musculus musculus (from central Europe) and Mus musculus castaneus (from southern Asia) are also represented genetically. These subspecies have hybridized to produce combinations of musculus and domesticus nuclear DNA coupled with domesticus mtDNA, and castaneus or musculus mtDNA with domesticus nuclear DNA. The majority of the mice with domesticus mtDNA that we sampled had d -loop sequences identical to two haplotypes common in Britain. This is consistent with long-term British–New Zealand cultural linkages. The origins of the castaneus mtDNA sequences widespread in New Zealand are less easy to identify.

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12

Soini, Helena A., Donald Wiesler, Sachiko Koyama, Christophe Féron, Claude Baudoin y Milos V. Novotny. "Comparison of Urinary Scents of Two Related Mouse Species, Mus spicilegus and Mus domesticus". Journal of Chemical Ecology 35, n.º 5 (24 de abril de 2009): 580–89. http://dx.doi.org/10.1007/s10886-009-9628-2.

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13

Vanlerberghe, F., B. Dod, P. Boursot, M. Bellis y F. Bonhomme. "Absence of Y-chromosome introgression across the hybrid zone between Mus musculus domesticus and Mus musculus musculus". Genetical Research 48, n.º 3 (diciembre de 1986): 191–97. http://dx.doi.org/10.1017/s0016672300025003.

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SummaryA cloned Y-specific sequence (Bishop et al. 1985) was used as a diagnostic probe to distinguish between Mus musculus domesticus and Mus musculus musculusY-chromosomes. Analysis of the RFLPs obtained with genomic DNA isolated from wild mice caught along the contact zone between M. m. domesticus and M. m. musculus in Bulgaria and Denmark showed that the Y-chromosome flow between the two semi-species is very limited. The degree of Y-chromosome penetration was compared with that of seven diagnostic autosomal loci and the mitochondrial DNA. Breeding experiments showed that the lack of Y-chromosome introgression from one semispecies to the other was not due to a major hybrid breakdown. The results suggest that the disruption of differentiated co-adapted gene systems could play a role in limiting Y-introgression.

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14

Tucker, P. K., B. K. Lee y E. M. Eicher. "Y chromosome evolution in the subgenus Mus (genus Mus)." Genetics 122, n.º 1 (1 de mayo de 1989): 169–79. http://dx.doi.org/10.1093/genetics/122.1.169.

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Abstract A 305 base pair DNA sequence isolated from the Y chromosome of the inbred mouse strain C57BL/10 was used to investigate the pattern and tempo of evolution of Y chromosome DNA sequences for five species in the subgenus Mus, including Mus spretus, Mus hortulanus, Mus abbotti, Mus musculus and Mus domesticus. Variation in hybridization patterns between species was characterized by differences in fragment lengths of both intensely and faintly hybridizing fragments, whereas variation in hybridization patterns within species was characterized primarily by differences in fragment lengths of faintly hybridizing fragments. Phylogenetic analyses were conducted based on fragment size variation within and among species. Phylogenetic relationships inferred from these analyses partly agree with the phylogenetic relationships obtained from biochemical and mitochondrial DNA data. We conclude that a set of DNA sequences common to the Y chromosomes of a closely related group of species in the subgenus Mus has evolved rapidly as reflected by sequence divergence and sequence amplification.

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15

SAGE, RICHARD D., ELLEN M. PRAGER, HERBERT TICHY y ALLAN C. WILSON. "Mitochondrial DNA variation in house mice, Mus domesticus (Rutty)". Biological Journal of the Linnean Society 41, n.º 1-3 (septiembre de 1990): 105–23. http://dx.doi.org/10.1111/j.1095-8312.1990.tb00824.x.

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16

Capanna, E. y R. Castiglia. "Chromosomes and speciation in Mus musculus domesticus". Cytogenetic and Genome Research 105, n.º 2-4 (2004): 375–84. http://dx.doi.org/10.1159/000078210.

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17

Walker, Curt y John A. Byers. "Heritability of locomotor play in house mice, Mus domesticus". Animal Behaviour 42, n.º 6 (diciembre de 1991): 891–97. http://dx.doi.org/10.1016/s0003-3472(05)80141-1.

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18

Foo, Colin, Julianne Farrell, Annika Boxell, Ian Robertson y Una M. Ryan. "Novel Cryptosporidium Genotype in Wild Australian Mice (Mus domesticus)". Applied and Environmental Microbiology 73, n.º 23 (5 de octubre de 2007): 7693–96. http://dx.doi.org/10.1128/aem.00848-07.

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ABSTRACT A total of 250 mouse fecal specimens collected from crop farms in Queensland, Australia, were screened for the presence of Cryptosporidium spp. using PCR. Of these, 19 positives were detected and characterized at a number of loci, including the 18S rRNA gene, the acetyl coenzyme A gene, and the actin gene. Sequence and phylogenetic analyses identified two genotypes: mouse genotype I and a novel genotype (mouse genotype II), which is likely to be a valid species. Cryptosporidium parvum, which is zoonotic, was not detected. The results of the study indicate that wild Australian mice that are not in close contact with livestock are probably not an important reservoir of Cryptosporidium infection for humans and other animals.

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19

Hurst, Jane L. "Mating in free-living wild House mice (Mus domesticus)". Journal of Zoology 210, n.º 4 (20 de agosto de 2009): 623–28. http://dx.doi.org/10.1111/j.1469-7998.1986.tb03663.x.

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20

Pouliquen, Odile, Michelle Leishman y Trevor D. Redhead. "Effects of radio collars on wild mice, Mus domesticus". Canadian Journal of Zoology 68, n.º 7 (1 de julio de 1990): 1607–9. http://dx.doi.org/10.1139/z90-239.

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Experiments were conducted in the laboratory and in the field to test the effects of radio collars (1.7–1.9 g) on wild house mice (Mus domesticus). There was a decrease in the activity of the collared animals in the laboratory immediately after collar attachment. There were no adverse effects on social interactions in the laboratory, nor on survival for 4–5 days in the field. Provided that the collar is well adjusted, there should be no need to keep wild animals captive for more than 1 h after collar attachment. These results are consistent with those of other researchers on the effect of transmitters on some species of small mammals.

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21

MCCARTHY, M. "Oxytocin inhibits infanticide in female house mice (Mus domesticus)". Hormones and Behavior 24, n.º 3 (septiembre de 1990): 365–75. http://dx.doi.org/10.1016/0018-506x(90)90015-p.

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22

Chen, Q. C., D. Cain y P. H. Jen. "Sound pressure transformation at the pinna of Mus domesticus." Journal of Experimental Biology 198, n.º 9 (1 de septiembre de 1995): 2007–23. http://dx.doi.org/10.1242/jeb.198.9.2007.

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Sound pressure transformation properties at the pinna of laboratory mice Mus domesticus were studied by measuring the sound pressure level of a continuous tone at a series of frequencies at the tympanic membrane as a function of the position of a sound source under free-field stimulation conditions. The spectral transformation, the interaural spectral difference, the isopressure contours and the interaural pressure difference contours were plotted. Sound pressure transformation functions showed some prominent spectral notches throughout the frequency range tested (10-80 kHz). However, the notch frequency did not appear to be systematically related to sound direction. The study of interaural pressure difference demonstrated that, when delivered from some angles within the ipsilateral frontal hemisphere, the sound pressure at the tympanic membrane of certain frequencies may be lower than that determined at the corresponding contralateral angles. For each sound frequency tested, there was an angle (the acoustic axis) within the ipsilateral frontal hemisphere from which the delivered sound reached a maximal pressure level at the tympanic membrane. However, the acoustic axis often changed to a new angle after removal of the ipsilateral pinna. In addition, sound delivered from the acoustic axis did not always generate a maximal pressure transformation. The isopressure contours determined within 2-5 dB of the maximal pressure were circumscribed, and their contained angular areas were found to decrease with increasing sound frequency. The 2 dB maximal pressure area may appear at more than one angular area for some test frequencies. Removal of the ipsilateral pinna or modification of pinna posture expanded isopressure contours irregularly and split the 2 dB maximal pressure area into several parts. The sound pressure difference determined between the angles of maximal and minimal sound pressure (the maximal directionality) increased with sound frequency regardless of pinna posture. Acoustic gain of the pinna at the acoustic axis reached 6-12 dB, depending upon sound frequency. However, the pinna gain was not always maximal at the acoustic axis for a given frequency.

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23

Gregorova, S., P. Divina, R. Storchova, Z. Trachtulec, V. Fotopulosova, K. L. Svenson, L. R. Donahue, B. Paigen y J. Forejt. "Mouse consomic strains: Exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies". Genome Research 18, n.º 3 (6 de febrero de 2008): 509–15. http://dx.doi.org/10.1101/gr.7160508.

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24

Bishop, C. E., P. Boursot, B. Baron, F. Bonhomme y D. Hatat. "Most classical Mus musculus domesticus laboratory mouse strains carry a Mus musculus musculus Y chromosome". Nature 315, n.º 6014 (mayo de 1985): 70–72. http://dx.doi.org/10.1038/315070a0.

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25

Blank, R. D., G. R. Campbell y P. D′Eustachio. "POSSIBLE DERIVATION OF THE LABORATORY MOUSE GENOME FROM MULTIPLE WILD MUS SPECIES". Genetics 114, n.º 4 (1 de diciembre de 1986): 1257–69. http://dx.doi.org/10.1093/genetics/114.4.1257.

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ABSTRACT Laboratory strains of mice are thought to be derived from wild populations of Mus domesticus. Many instances of non-domesticus genetic information fixed in these strains have been described, however, and the amount of strain-to-strain genetic variation exceeds that found in wild domesticus populations. In order to estimate the extent of the non-domesticus contribution to laboratory mouse genomes, and to determine whether it could account for observed variation, we have used computer simulations to investigate the properties of genetically marked chromosomal segments and the distribution of residual allogenicity at various times during inbreeding. A locus or chromosomal segment is allogenic if it is unfixed within a lineage at a given time. The odds of fixation of a foreign chromosome segment are predicted to be an exponentially decreasing function of its length. The median segment length is predicted to be 17 centimorgans. Available data for markers of chromosomes 1, 9 and 12 in recombinant inbred strain sets conform to these predictions. Together, the results suggest that introgression of non-domesticus chromosomes and segregation of residual allogenicity are sufficient to account for the genetic diversity observed among inbred mouse strains and substrains.

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26

Osuna, Alexander Nivia. "Sobrevivência in vitro de blastocistos Mus domesticus domesticus vitrificados em macro ou microvolume de crioprotetor". Acta Scientiae Veterinariae 36, n.º 3 (30 de marzo de 2018): 333. http://dx.doi.org/10.22456/1679-9216.17324.

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27

Dickman, C. R. "Predation and Habitat Shift in the House Mouse, Mus Domesticus". Ecology 73, n.º 1 (febrero de 1992): 313–22. http://dx.doi.org/10.2307/1938742.

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28

Palanza, P. y S. Parmigiani. "Male and female infanticide in Swiss albino mice (Mus domesticus)". Ethology Ecology & Evolution 2, n.º 3 (septiembre de 1990): 319–20. http://dx.doi.org/10.1080/08927014.1990.9525457.

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29

Kronenberger, J. P. y J. Médioni. "Food neophobia in wild and laboratory mice (Mus musculus domesticus)". Behavioural Processes 11, n.º 1 (junio de 1985): 53–59. http://dx.doi.org/10.1016/0376-6357(85)90102-0.

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30

Novotny, M., S. Harvey y B. Jemiolo. "Chemistry of male dominance in the house mouse,Mus domesticus". Experientia 46, n.º 1 (enero de 1990): 109–13. http://dx.doi.org/10.1007/bf01955433.

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31

Orth, Annie, Khalid Belkhir, Janice Britton-Davidian, Pierre Boursot, Touria Benazzou y François Bonhomme. "Hybridation naturelle entre deux espèces sympatriques de souris Mus musculus domesticus L. et Mus spretus Lataste". Comptes Rendus Biologies 325, n.º 2 (febrero de 2002): 89–97. http://dx.doi.org/10.1016/s1631-0691(02)01413-0.

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32

Le Roy, Isabelle, Pierre L. Roubertoux, Laure Jamot, Fatima Maarouf, Sylvie Tordjman, Stéphane Mortaud, Caroline Blanchard, Benoit Martin, Pascale-Valérie Guillot y Vincent Duquenne. "Neuronal and behavioral differences between Mus musculus domesticus (C57BL/6JBy) and Mus musculus castaneus (CAST/Ei)". Behavioural Brain Research 95, n.º 1 (septiembre de 1998): 135–42. http://dx.doi.org/10.1016/s0166-4328(97)00218-0.

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33

Casavant, N. C., S. C. Hardies, F. D. Funk, M. B. Comer, M. H. Edgell y C. A. Hutchison. "Extensive movement of LINES ONE sequences in beta-globin loci of Mus caroli and Mus domesticus." Molecular and Cellular Biology 8, n.º 11 (noviembre de 1988): 4669–74. http://dx.doi.org/10.1128/mcb.8.11.4669.

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LINES ONE (L1) is a family of movable DNA sequences found in mammals. To measure the rate of their movement, we have compared the positions of L1 elements within homologous genetic loci that are separated by known divergence times. Two models that predict different outcomes of this analysis have been proposed for the behavior of L1 sequences. (i) Previous theoretical studies of concerted evolution in L1 have indicated that the majority of the 100,000 extant L1 elements may have inserted as recently as within the last 3 million years. (ii) Gene conversion has been proposed as an alternative to a history of prolific recent insertions. To distinguish between these two models, we cloned and characterized two embryonic beta-globin haplotypes from Mus caroli and compared them with those of M. domesticus. In 9 of 10 instances, we observed an L1 element to be present in one chromosome and absent at the same site in a homologous chromosome. This frequency is quantitatively consistent with the known rate of concerted evolution. Therefore, we conclude that gene conversion is not required for concerted evolution of the L1 family in the mouse. Furthermore, we show that the extensive movement of L1 sequences contributes to restriction fragment length polymorphism. L1 insertions may be the predominant cause of restriction fragment length polymorphisms in closely related haplotypes.

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34

Rikke, Brad A. y Stephen C. Hardies. "LINE-1 repetitive DNA probes for species-specific cloning from Mus spretus and Mus domesticus genomes". Genomics 11, n.º 4 (diciembre de 1991): 895–904. http://dx.doi.org/10.1016/0888-7543(91)90012-4.

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35

Casavant, N. C., S. C. Hardies, F. D. Funk, M. B. Comer, M. H. Edgell y C. A. Hutchison. "Extensive movement of LINES ONE sequences in beta-globin loci of Mus caroli and Mus domesticus". Molecular and Cellular Biology 8, n.º 11 (noviembre de 1988): 4669–74. http://dx.doi.org/10.1128/mcb.8.11.4669-4674.1988.

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LINES ONE (L1) is a family of movable DNA sequences found in mammals. To measure the rate of their movement, we have compared the positions of L1 elements within homologous genetic loci that are separated by known divergence times. Two models that predict different outcomes of this analysis have been proposed for the behavior of L1 sequences. (i) Previous theoretical studies of concerted evolution in L1 have indicated that the majority of the 100,000 extant L1 elements may have inserted as recently as within the last 3 million years. (ii) Gene conversion has been proposed as an alternative to a history of prolific recent insertions. To distinguish between these two models, we cloned and characterized two embryonic beta-globin haplotypes from Mus caroli and compared them with those of M. domesticus. In 9 of 10 instances, we observed an L1 element to be present in one chromosome and absent at the same site in a homologous chromosome. This frequency is quantitatively consistent with the known rate of concerted evolution. Therefore, we conclude that gene conversion is not required for concerted evolution of the L1 family in the mouse. Furthermore, we show that the extensive movement of L1 sequences contributes to restriction fragment length polymorphism. L1 insertions may be the predominant cause of restriction fragment length polymorphisms in closely related haplotypes.

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36

Assaf, Sabrina Silveira y José Luiz Rodrigues. "Vitrificação de embriões Mus domesticus domesticus contidos em volumes diferentes de 9,0 M de etileno glicol". Revista Brasileira de Ciência Veterinária 13, n.º 2 (2006): 131–36. http://dx.doi.org/10.4322/rbcv.2014.285.

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37

Rheaume, C., K. W. Barbour, J. Tseng-Crank y F. G. Berger. "Molecular genetics of androgen-inducible RP2 gene transcription in the mouse kidney." Molecular and Cellular Biology 9, n.º 2 (febrero de 1989): 477–83. http://dx.doi.org/10.1128/mcb.9.2.477.

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Androgen control of the RP2 gene in the mouse kidney has been modified during evolution. In inbred mice (Mus domesticus), the concentrations of mRNAs encoded by RP2 undergo a 10- to 12-fold induction in response to testosterone; in other Mus species (e.g., Mus hortulanus and Mus caroli), induction ranges from none to about two- to fourfold. In this communication, we show that androgens induced RP2 transcription in M. domesticus, although this induction may not have fully accounted for the increase in mRNA levels. Reduced mRNA inducibility in M. hortulanus and in several other species was associated with an absence of transcriptional induction. Analysis of an interspecies backcross population indicated that the difference in RP2 inducibility between M. domesticus and M. hortulanus was due to a single Mendelian locus tightly linked (0 of 47 recombinants) to RP2. The RP2 gene was found to contain at least two promoters, only one of which was highly sensitive to testosterone. These results indicate that induction of the RP2 mRNAs, as well as interspecies variations in RP2 inducibility, are primarily a consequence of effects on this promoter.

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38

Rheaume, C., K. W. Barbour, J. Tseng-Crank y F. G. Berger. "Molecular genetics of androgen-inducible RP2 gene transcription in the mouse kidney". Molecular and Cellular Biology 9, n.º 2 (febrero de 1989): 477–83. http://dx.doi.org/10.1128/mcb.9.2.477-483.1989.

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Androgen control of the RP2 gene in the mouse kidney has been modified during evolution. In inbred mice (Mus domesticus), the concentrations of mRNAs encoded by RP2 undergo a 10- to 12-fold induction in response to testosterone; in other Mus species (e.g., Mus hortulanus and Mus caroli), induction ranges from none to about two- to fourfold. In this communication, we show that androgens induced RP2 transcription in M. domesticus, although this induction may not have fully accounted for the increase in mRNA levels. Reduced mRNA inducibility in M. hortulanus and in several other species was associated with an absence of transcriptional induction. Analysis of an interspecies backcross population indicated that the difference in RP2 inducibility between M. domesticus and M. hortulanus was due to a single Mendelian locus tightly linked (0 of 47 recombinants) to RP2. The RP2 gene was found to contain at least two promoters, only one of which was highly sensitive to testosterone. These results indicate that induction of the RP2 mRNAs, as well as interspecies variations in RP2 inducibility, are primarily a consequence of effects on this promoter.

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39

González, Marisel, Raúl Fernández-Donoso y Soledad Berríos. "Apoptosis in Spermiogenesis of Multiple Robertsonian Heterozygotes of Mus musculus domesticus". International Journal of Medical and Surgical Sciences 2, n.º 4 (26 de octubre de 2018): 589–601. http://dx.doi.org/10.32457/ijmss.2015.035.

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Mus musculus domesticus is a species that is characterized by a diploid number of 40 chromosomes, all telocentrics (acrocentrics). In natural populations of Mus with high frequency Robertsonian chromosome translocations (RBs), a fusion at centromere-level between two autosomal telocentric, producing metacentric Rb chromosomes and a variety of natural subspecies with diploid chromosome numbers below 40. Rb chromosomes do not affect the viability of individuals but mainly fertility of Rb heterozygotes. In their meiosis the metacentric Rb and the homologous telocentrics form trivalents that have problems in synapsis and segregation. This paper presents a comparative analysis of spermatogenesis considering the stages of the epithelium and the number of germ cells loss by apoptosis comparing heterozygote males 2n=32, carriers 8 trivalents, and homozygotes 2n=40 and 2n=24. It was found that the number of spermatocytes in first prophase was similar in the different seminiferous epithelium stages in all the chromosome constitutions. In the 2n=32 heterozygotes a significant decreased number of spermatids was reflected in the proportion of spermatocytes and spermatids that was 1:1.7. In the homozygote males rare germ cell in apoptosis (positive for caspase 3) were observed, which were mainly concentrated in the XII stage of the seminiferous epithelium. In heterozygote spermatocytes apoptotic germ cell number was significantly higher than that registered in homozygote males, and generally correspond to spermatocytes in meiotic divisions. This selective removal of cells possibly carrying anomalies, either in chromosome alignment or segregation, is consistent with the smaller number of spermatids and the relative sub-fertility observed in 2n=32 Rb heterozygotes.

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SCHMID-HOLMES, SABINE, LEE C. DRICKAMER, AMI SESSIONS ROBINSON y LYNN L. GILLIE. "Burrows and Burrow-Cleaning Behavior of House Mice (Mus musculus domesticus)". American Midland Naturalist 146, n.º 1 (julio de 2001): 53–62. http://dx.doi.org/10.1674/0003-0031(2001)146[0053:babcbo]2.0.co;2.

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41

Elwood, Robert W., Dawn Masterson y Carol O'Neill. "Protecting pups in tests for infanticidal responsiveness in mice, Mus domesticus". Animal Behaviour 40, n.º 4 (octubre de 1990): 778–80. http://dx.doi.org/10.1016/s0003-3472(05)80708-0.

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42

TATTERSALL, F. H., F. NOWELL y R. H. SMITH. "A review of the endoparasites of wild House Mice Mus domesticus". Mammal Review 24, n.º 2 (junio de 1994): 61–71. http://dx.doi.org/10.1111/j.1365-2907.1994.tb00135.x.

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43

Baker, Ann Eileen Miller y Michael L. Petras. "The fate of Mus domesticus demes after destruction of their habitats". Biological Journal of the Linnean Society 29, n.º 2 (octubre de 1986): 81–88. http://dx.doi.org/10.1111/j.1095-8312.1986.tb01823.x.

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44

Coleman, Mark A., Theodore Garland, Catherine A. Marler, Stephen S. Newton, John G. Swallow y Patrick A. Carter. "Glucocorticoid Response to Forced Exercise in Laboratory House Mice (Mus domesticus)". Physiology & Behavior 63, n.º 2 (enero de 1998): 279–85. http://dx.doi.org/10.1016/s0031-9384(97)00441-1.

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45

KABOODVANDPOUR, Shahram y Luke K. P. LEUNG. "Managing crop damage caused by house mice (Mus domesticus) in Australia". Integrative Zoology 5, n.º 1 (marzo de 2010): 2–14. http://dx.doi.org/10.1111/j.1749-4877.2010.00188.x.

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46

Laviola, Giovanni y Enrico Alleva. "Sibling effects on the behavior of infant mouse litters (Mus domesticus)." Journal of Comparative Psychology 109, n.º 1 (1995): 68–75. http://dx.doi.org/10.1037/0735-7036.109.1.68.

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47

Mossman, Catherine A. y Lee C. Drickamer. "Odor preferences of female house mice (Mus domesticus) in seminatural enclosures." Journal of Comparative Psychology 110, n.º 2 (1996): 131–38. http://dx.doi.org/10.1037/0735-7036.110.2.131.

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48

Drickamer, Lee C., Frederick S. Vom Saal, Lisa M. Marriner y Catherine A. Mossman. "Anogenital distance and dominance status in male house mice (Mus domesticus)". Aggressive Behavior 21, n.º 4 (1995): 301–9. http://dx.doi.org/10.1002/1098-2337(1995)21:4<301::aid-ab2480210406>3.0.co;2-1.

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49

GRAY, SAMANTHA J. y JANE L. HURST. "Competitive behaviour in an island population of house mice,Mus domesticus". Animal Behaviour 56, n.º 5 (noviembre de 1998): 1291–99. http://dx.doi.org/10.1006/anbe.1998.0890.

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50

Twigg, LE y BJ Kay. "Effect of flooding on field populations of house mice (Mus domesticus)". Wildlife Research 19, n.º 2 (1992): 145. http://dx.doi.org/10.1071/wr9920145.

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