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果蝇卵母细胞中内源性oskarmRNA颗粒的组装用于依赖运动蛋白的运输。

Assembly of endogenous oskar mRNA particles for motor-dependent transport in the Drosophila oocyte.

作者信息

Trucco Alvar, Gaspar Imre, Ephrussi Anne

机构信息

Developmental Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.

出版信息

Cell. 2009 Nov 25;139(5):983-98. doi: 10.1016/j.cell.2009.10.012.

Abstract

oskar mRNA localization at the oocyte posterior pole is essential for correct patterning of the Drosophila embryo. Here we show at the ultrastructural level that endogenous oskar ribonucleoprotein complexes (RNPs) assemble sequentially with initial recruitment of Hrp48 and the exon junction complex (EJC) to oskar transcripts in the nurse cell nuclei, and subsequent recruitment of Staufen and microtubule motors, following transport to the cytoplasm. oskar particles are non-membrane-bound structures that coalesce as they move from the oocyte anterior to the posterior pole. Our analysis uncovers a role for the EJC component Barentsz in recruiting Tropomyosin II (TmII) to oskar particles in the ooplasm and reveals that TmII is required for kinesin binding to the RNPs. Finally, we show that both kinesin and dynein associate with oskar particles and are the primary microtubule motors responsible for transport of the RNPs within the oocyte.

摘要

osk mRNA定位于卵母细胞后极对于果蝇胚胎的正确模式形成至关重要。在这里,我们在超微结构水平上表明,内源性osk核糖核蛋白复合物(RNP)在滋养细胞核中与Hrp48和外显子连接复合物(EJC)最初募集到osk转录本上,并在运输到细胞质后随后募集Staufen和微管马达,从而依次组装。osk颗粒是无膜结合结构,当它们从卵母细胞前部移动到后极时会聚集在一起。我们的分析揭示了EJC组分Barentsz在将原肌球蛋白II(TmII)募集到卵质中的osk颗粒中的作用,并表明TmII是驱动蛋白与RNP结合所必需的。最后,我们表明驱动蛋白和动力蛋白都与osk颗粒相关联,并且是负责卵母细胞内RNP运输的主要微管马达。

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