Cohesin component dynamics during meiotic prophase I in mammalian oocytes

被引:0
作者
Ignacio Prieto
Charles Tease
Nieves Pezzi
José M. Buesa
Sagrario Ortega
Leonor Kremer
Alicia Martínez
Carlos Martínez-A
Maj A. Hultén
José L. Barbero
机构
[1] Centro Nacional de Biotecnología/CSIC,Department of Immunology and Oncology
[2] UAM Campus de Cantoblanco,Department of Biological Sciences
[3] University of Warwick,undefined
[4] Centro Nacional de Investigaciones Oncológic,undefined
来源
Chromosome Research | 2004年 / 12卷
关键词
chromatid cohesion; chromosome segregation; dictyate; mammal; meiosis;
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摘要
Cohesins are chromosomal proteins that form complexes involved in the maintenance of sister chromatid cohesion during division of somatic and germ cells. Three meiosis-specific cohesin subunits have been reported in mammals, REC8, STAG3 and SMC1β; their expression in mouse spermatocytes has also been described. Here we studied the localization of different meiotic and mitotic cohesin components during prophase I in human and murine female germ cells. In normal and atretic human fetal oocytes, from leptotene to diplotene stages, REC8 and STAG3 colocalize in fibers. In murine oocytes, SMC1β, SMC3 and STAG3 are localized along fibers that correspond first to the chromosome axis and then to the synaptonemal complex in pachytene. Mitotic cohesin subunit RAD21 is also found in fibers that decorate the SC during prophase I in mouse oocytes, suggesting a role for this cohesin in mammalian sister chromatid cohesion in female meiosis. We observed that, unlike human oocytes, murine synaptonemal complex protein SYCP3 localizes to nucleoli throughout prophase I stages, and centromeres cluster in discrete locations from leptotene to dictyate. At difference from meiosis in male mice, the cohesin axis is progressively lost during the first week after birth in females with a parallel destruction of the axial elements at dictyate arrest, demonstrating sexual dimorphism in sister chromatid cohesion in meiosis.
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页码:197 / 213
页数:16
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