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The Nucleoporin Nup2 Contains a Meiotic-Autonomous Region that Promotes the Dynamic Chromosome Events of Meiosis

机译:核蛋白Nup2包含一个减数分裂自治区可促进减数分裂的动态染色体事件。

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摘要

Meiosis is a specialized cellular program required to create haploid gametes from diploid parent cells. Homologous chromosomes pair, synapse, and recombine in a dynamic environment that accommodates gross chromosome reorganization and significant chromosome motion, which are critical for normal chromosome segregation. In Saccharomyces cerevisiae, Ndj1 is a meiotic telomere-associated protein required for physically attaching telomeres to proteins embedded in the nuclear envelope. In this study, we identified additional proteins that act at the nuclear periphery from meiotic cell extracts, including Nup2, a nonessential nucleoporin with a known role in tethering interstitial chromosomal loci to the nuclear pore complex. We found that deleting NUP2 affects meiotic progression and spore viability, and gives increased levels of recombination intermediates and products. We identified a previously uncharacterized 125 aa region of Nup2 that is necessary and sufficient for its meiotic function, thus behaving as a meiotic autonomous region (MAR). Nup2-MAR forms distinct foci on spread meiotic chromosomes, with a subset overlapping with Ndj1 foci. Localization of Nup2-MAR to meiotic chromosomes does not require Ndj1, nor does Ndj1 localization require Nup2, suggesting these proteins function in different pathways, and their interaction is weak or indirect. Instead, several severe synthetic phenotypes are associated with the nup2Δ ndj1Δ double mutant, including delayed turnover of recombination joint molecules, and a failure to undergo nuclear divisions without also arresting the meiotic program. These data suggest Nup2 and Ndj1 support partially overlapping functions that promote two different levels of meiotic chromosome organization necessary to withstand a dynamic stage of the eukaryotic life cycle.
机译:减数分裂是从二倍体亲代细胞产生单倍体配子所需的专门细胞程序。同源染色体在动态环境中配对,突触和重组,该环境适应总体染色体重组和明显的染色体运动,这对于正常的染色体分离至关重要。在酿酒酵母中,Ndj1是与减数分裂端粒相关的蛋白,可将端粒物理连接到包埋在核膜中的蛋白上。在这项研究中,我们从减数分裂细胞提取物中鉴定了作用于核外围的其他蛋白质,包括Nup2,一种非必需核孔蛋白,在将间质染色体基因座束缚到核孔复合体中具有已知作用。我们发现删除NUP2影响减数分裂进程和孢子活力,并提供增加水平的重组中间体和产品。我们确定了Nup2以前未知的125aa区域,该区域对于其减数分裂功能是必要和充分的,因此表现为减数分裂自治区(MAR)。 Nup2-MAR在减数分裂的染色体上形成明显的病灶,其子集与Ndj1病灶重叠。 Nup2-MAR定位到减数分裂染色体不需要Ndj1,也不需要Ndj1定位也不需要Nup2,这表明这些蛋白以不同的途径起作用,它们的相互作用是弱的或间接的。取而代之的是,几种严重的合成表型与nup2Δndj1Δ双突变体相关,包括重组关节分子的延迟更新,以及在不停止减数分裂程序的情况下无法进行核分裂。这些数据表明Nup2和Ndj1支持部分重叠的功能,这些功能可促进两个不同水平的减数分裂染色体组织,以承受真核生物生命周期的动态阶段。

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