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PIWI/AGO蛋白MIWI与驱动蛋白KIF17b在雄性生殖细胞类染色质体中的相互作用。

Interplay of PIWI/Argonaute protein MIWI and kinesin KIF17b in chromatoid bodies of male germ cells.

作者信息

Kotaja Noora, Lin Haifan, Parvinen Martti, Sassone-Corsi Paolo

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, B.P. 10142, 67404 Illkirch-Strasbourg, France.

出版信息

J Cell Sci. 2006 Jul 1;119(Pt 13):2819-25. doi: 10.1242/jcs.03022.

Abstract

Chromatoid bodies are thought to act as male-germ-cell-specific platforms for the storing and processing of haploid transcripts. The molecular mechanisms governing the formation and function of these germ-cell-specific structures have remained elusive. In this study, we show that the kinesin motor protein KIF17b, which is involved in the nucleocytoplasmic transport of RNA and of a transcriptional coactivator, localizes in chromatoid bodies. The chromatoid body moves actively and non-randomly in the cytoplasm of round spermatids, making frequent contacts with the nuclear envelope. The localization of KIF17b thereby offers a potential mechanism for microtubule-dependent mobility of chromatoid bodies, as well as for the transport of the specific components in and out of the chromatoid body. Interestingly, we demonstrate that KIF17b physically interacts with a testis-specific member of the PIWI/Argonaute family, MIWI, a component of chromatoid bodies implicated in RNA metabolism. A functional interplay between KIF17b and MIWI might be needed for the loading of haploid RNAs in the chromatoid body. Importantly, chromatoid bodies from round spermatids of miwi-null mice are not fully compacted and remain as a diffuse chromatoid material, revealing the essential role played by MIWI in the formation of chromatoid bodies. These results shed new light on the function of chromatoid bodies in the post-transcriptional regulation of gene expression in haploid germ cells.

摘要

拟染色体被认为是作为单倍体转录本储存和加工的雄性生殖细胞特异性平台。调控这些生殖细胞特异性结构形成和功能的分子机制仍不清楚。在本研究中,我们发现参与RNA和转录共激活因子核质运输的驱动蛋白KIF17b定位于拟染色体。拟染色体在圆形精子细胞的细胞质中活跃且非随机地移动,频繁与核膜接触。KIF17b的定位因此为拟染色体的微管依赖性移动以及特定成分进出拟染色体的运输提供了一种潜在机制。有趣的是,我们证明KIF17b与PIWI/Argonaute家族的睾丸特异性成员MIWI发生物理相互作用,MIWI是拟染色体中参与RNA代谢的一个成分。拟染色体中装载单倍体RNA可能需要KIF17b和MIWI之间的功能相互作用。重要的是,来自miwi基因敲除小鼠圆形精子细胞的拟染色体没有完全压实,仍为弥散的拟染色体物质,揭示了MIWI在拟染色体形成中所起的重要作用。这些结果为拟染色体在单倍体生殖细胞基因表达的转录后调控中的功能提供了新的见解。

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