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Genetic Interactions Between the Meiosis-Specific Cohesin Components STAG3 REC8 and RAD21L

机译:减数分裂特异性黏附素成分STAG3REC8和RAD21L之间的遗传相互作用

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摘要

Cohesin is an essential structural component of chromosomes that ensures accurate chromosome segregation during mitosis and meiosis. Previous studies have shown that there are cohesin complexes specific to meiosis, required to mediate homologous chromosome pairing, synapsis, recombination, and segregation. Meiosis-specific cohesin complexes consist of two structural maintenance of chromosomes proteins (SMC1α/SMC1β and SMC3), an α-kleisin protein (RAD21, RAD21L, or REC8), and a stromal antigen protein (STAG1, 2, or 3). STAG3 is exclusively expressed during meiosis, and is the predominant STAG protein component of cohesin complexes in primary spermatocytes from mouse, interacting directly with each α-kleisin subunit. REC8 and RAD21L are also meiosis-specific cohesin components. Stag3 mutant spermatocytes arrest in early prophase (“zygotene-like” stage), displaying failed homolog synapsis and persistent DNA damage, as a result of unstable loading of cohesin onto the chromosome axes. Interestingly, Rec8, Rad21L double mutants resulted in an earlier “leptotene-like” arrest, accompanied by complete absence of STAG3 loading. To assess genetic interactions between STAG3 and α-kleisin subunits RAD21L and REC8, our lab generated Stag3, Rad21L, and Stag3, Rec8 double knockout mice, and compared them to the Rec8, Rad21L double mutant. These double mutants are phenotypically distinct from one another, and more severe than each single knockout mutant with regards to chromosome axis formation, cohesin loading, and sister chromatid cohesion. The Stag3, Rad21L, and Stag3, Rec8 double mutants both progress further into prophase I than the Rec8, Rad21L double mutant. Our genetic analysis demonstrates that cohesins containing STAG3 and REC8 are the main complex required for centromeric cohesion, and RAD21L cohesins are required for normal clustering of pericentromeric heterochromatin. Furthermore, the STAG3/REC8 and STAG3/RAD21L cohesins are the primary cohesins required for axis formation.
机译:粘着蛋白是染色体的重要结构组成部分,可确保有丝分裂和减数分裂过程中染色体的正确分离。先前的研究表明,介导同源染色体配对,突触,重组和分离所需的减数分裂特异的粘着蛋白复合物。减数分裂特异的粘着蛋白复合物由两个结构上的染色体蛋白(SMC1α/SMC1β和SMC3),一个α-kleisin蛋白(RAD21,RAD21L或REC8)和一个基质抗原蛋白(STAG1、2或3)组成。 STAG3仅在减数分裂过程中表达,并且是小鼠原代精母细胞黏附素复合物中STAG蛋白的主要成分,可直接与每个α-kleisin亚基相互作用。 REC8和RAD21L也是减数分裂特有的黏附素成分。 Stag3突变的精母细胞在早期(“合子样”阶段)停滞,显示出失败的同源突触和持续的DNA损伤,这是由于粘着蛋白在染色体轴上的不稳定加载所致。有趣的是,Rec8,Rad21L双突变体导致更早的“瘦素样”停滞,并伴有完全不存在STAG3的情况。为了评估STAG3与α-kleisin亚基RAD21L和REC8之间的遗传相互作用,我们的实验室产生了Stag3,Rad21L和Stag3,Rec8双敲除小鼠,并将它们与Rec8,Rad21L双突变体进行了比较。这些双突变体在表型上彼此不同,并且在染色体轴形成,粘着素负载和姐妹染色单体内聚力方面比每个单个敲除突变体更为严重。 Stag3,Rad21L和Stag3,Rec8双重突变体都比Rec8,Rad21L双重突变体更进一步进入前期I.我们的遗传分析表明,包含STAG3和REC8的黏着蛋白是着丝粒结合的主要复合物,而RAD21L黏着蛋白是着丝粒异构染色质正常聚簇所必需的。此外,STAG3 / REC8和STAG3 / RAD21L粘着蛋白是轴形成所需的主要粘着蛋白。

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