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Mago Nashi、Tsunagi/Y14 和 Ranshi 形成一个复合物,影响果蝇的卵母细胞分化。

Mago Nashi, Tsunagi/Y14, and Ranshi form a complex that influences oocyte differentiation in Drosophila melanogaster.

机构信息

Cell and Molecular Biology Graduate Program, Institute for Cell and Molecular Biology, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Dev Biol. 2010 Mar 15;339(2):307-19. doi: 10.1016/j.ydbio.2009.12.035. Epub 2010 Jan 4.

Abstract

During Drosophila melanogaster oogenesis, a germline stem cell divides forming a cyst of 16 interconnected cells. One cell enters the oogenic pathway, and the remaining 15 differentiate as nurse cells. Although directed transport and localization of oocyte differentiation factors within the single cell are indispensible for selection, maintenance, and differentiation of the oocyte, the mechanisms regulating these events are poorly understood. Mago Nashi and Tsunagi/Y14, core components of the exon junction complex (a multiprotein complex assembled on spliced RNAs), are essential for restricting oocyte fate to a single cell and for localization of oskar mRNA. Here we provide evidence that Mago Nashi and Tsunagi/Y14 form an oogenic complex with Ranshi, a protein with a zinc finger-associated domain and zinc finger domains. Genetic analyses of ranshi reveal that (1) 16-cell cysts are formed, (2) two cells retain synaptonemal complexes, (3) all cells have endoreplicated DNA (as observed in nurse cells), and (4) oocyte-specific cytoplasmic markers accumulate and persist within a single cell but are not localized within the posterior pole of the presumptive oocyte. Our results indicate that Ranshi interacts with the exon junction complex to localize components essential for oocyte differentiation within the posterior pole of the presumptive oocyte.

摘要

在黑腹果蝇的卵子发生过程中,生殖干细胞分裂形成一个由 16 个相互连接的细胞组成的小囊。其中一个细胞进入卵子发生途径,其余 15 个细胞分化为滋养细胞。尽管指导运输和卵母细胞分化因子在单细胞内的定位对于卵母细胞的选择、维持和分化是必不可少的,但调节这些事件的机制仍知之甚少。Mago Nashi 和 Tsunagi/Y14 是外显子结合复合物(组装在拼接 RNA 上的多蛋白复合物)的核心组成部分,对于限制卵母细胞命运为单个细胞以及定位 Oskar mRNA 是必需的。在这里,我们提供的证据表明,Mago Nashi 和 Tsunagi/Y14 与 Ranshi 形成一个卵子发生复合物,Ranshi 是一种具有锌指相关结构域和锌指结构域的蛋白质。ranshi 的遗传分析表明:(1)形成了 16 细胞小囊;(2)两个细胞保留联会复合体;(3)所有细胞都具有内复制 DNA(如在滋养细胞中观察到的);(4)卵母细胞特异性细胞质标记物在单个细胞内积累并持续存在,但不在预期卵母细胞的后极内定位。我们的结果表明,Ranshi 与外显子结合复合物相互作用,将对于卵母细胞分化至关重要的成分定位到预期卵母细胞的后极。

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