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α-内硫磷是果蝇卵母细胞减数分裂成熟所必需的一种保守蛋白。

alpha-Endosulfine is a conserved protein required for oocyte meiotic maturation in Drosophila.

作者信息

Von Stetina Jessica R, Tranguch Susanne, Dey Sudhansu K, Lee Laura A, Cha Byeong, Drummond-Barbosa Daniela

机构信息

Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

出版信息

Development. 2008 Nov;135(22):3697-706. doi: 10.1242/dev.025114. Epub 2008 Oct 16.

DOI:10.1242/dev.025114
PMID:18927152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2654389/
Abstract

Meiosis is coupled to gamete development and must be well regulated to prevent aneuploidy. During meiotic maturation, Drosophila oocytes progress from prophase I to metaphase I. The molecular factors controlling meiotic maturation timing, however, are poorly understood. We show that Drosophila alpha-endosulfine (endos) plays a key role in this process. endos mutant oocytes have a prolonged prophase I and fail to progress to metaphase I. This phenotype is similar to that of mutants of cdc2 (synonymous with cdk1) and of twine, the meiotic homolog of cdc25, which is required for Cdk1 activation. We found that Twine and Polo kinase levels are reduced in endos mutants, and identified Early girl (Elgi), a predicted E3 ubiquitin ligase, as a strong Endos-binding protein. In elgi mutant oocytes, the transition into metaphase I occurs prematurely, but Polo and Twine levels are unaffected. These results suggest that Endos controls meiotic maturation by regulating Twine and Polo levels, and, independently, by antagonizing Elgi. Finally, germline-specific expression of the human alpha-endosulfine ENSA rescues the endos mutant meiotic defects and infertility, and alpha-endosulfine is expressed in mouse oocytes, suggesting potential conservation of its meiotic function.

摘要

减数分裂与配子发育相关联,必须得到良好调控以防止非整倍体的产生。在减数分裂成熟过程中,果蝇卵母细胞从减数分裂前期I进入中期I。然而,控制减数分裂成熟时间的分子因素却知之甚少。我们发现果蝇α - 内硫素(endos)在这一过程中起关键作用。endos突变体卵母细胞的减数分裂前期I延长,无法进入中期I。这种表型与细胞周期蛋白依赖性激酶2(cdc2,与cdk1同义)和twine(cdc25的减数分裂同源物,Cdk1激活所必需)的突变体相似。我们发现endos突变体中Twine和Polo激酶水平降低,并鉴定出Early girl(Elgi),一种预测的E3泛素连接酶,作为一种与Endos紧密结合的蛋白。在elgi突变体卵母细胞中,向中期I的转变过早发生,但Polo和Twine水平不受影响。这些结果表明,Endos通过调节Twine和Polo水平以及独立地通过拮抗Elgi来控制减数分裂成熟。最后,人类α - 内硫素ENSA在生殖系中的特异性表达挽救了endos突变体的减数分裂缺陷和不育,并且α - 内硫素在小鼠卵母细胞中表达,表明其减数分裂功能可能具有保守性。

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本文引用的文献

1
The inhibition of polo kinase by matrimony maintains G2 arrest in the meiotic cell cycle.婚姻对polo激酶的抑制作用使减数分裂细胞周期维持在G2期停滞状态。
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Mitosis persists in the absence of Cdk1 activity when proteolysis or protein phosphatase activity is suppressed.当蛋白水解或蛋白磷酸酶活性受到抑制时,有丝分裂在没有Cdk1活性的情况下仍会持续。
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The Drosophila mitotic inhibitor Frühstart specifically binds to the hydrophobic patch of cyclins.果蝇有丝分裂抑制剂Frühstart特异性结合细胞周期蛋白的疏水区域。
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PKA, germ cells, and fertility.蛋白激酶A、生殖细胞与生育能力。
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6
The Cdc20 (Fzy)/Cdh1-related protein, Cort, cooperates with Fzy in cyclin destruction and anaphase progression in meiosis I and II in Drosophila.Cdc20(Fzy)/Cdh1相关蛋白Cort在果蝇减数分裂I和II的细胞周期蛋白破坏及后期进程中与Fzy协同作用。
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An active protein kinase A (PKA) is involved in meiotic arrest of rat growing oocytes.活性蛋白激酶A(PKA)参与大鼠生长中卵母细胞的减数分裂阻滞。
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The when and wheres of CDC25 phosphatases.细胞周期蛋白磷酸酶CDC25的作用时间和作用位置。
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Bruno inhibits the expression of mitotic cyclins during the prophase I meiotic arrest of Drosophila oocytes.布鲁诺在果蝇卵母细胞减数第一次分裂前期阻滞过程中抑制有丝分裂周期蛋白的表达。
Dev Cell. 2006 Jan;10(1):127-35. doi: 10.1016/j.devcel.2005.10.018.