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在果蝇生殖质组装过程中,内吞途径作用于俄耳甫斯蛋白的下游。

The endocytic pathway acts downstream of Oskar in Drosophila germ plasm assembly.

作者信息

Tanaka Tsubasa, Nakamura Akira

机构信息

Laboratory for Germline Development, RIKEN Center for Developmental Biology, Kobe, Hyogo 650-0047, Japan.

出版信息

Development. 2008 Mar;135(6):1107-17. doi: 10.1242/dev.017293. Epub 2008 Feb 13.

Abstract

Cell fate is often determined by the intracellular localization of RNAs and proteins. In Drosophila oocytes, oskar (osk) RNA localization and the subsequent Osk synthesis at the posterior pole direct the assembly of the pole plasm, where factors for the germline and abdomen formation accumulate. osk RNA produces two isoforms, long and short Osk, which have distinct functions in pole plasm assembly. Short Osk recruits downstream components of the pole plasm, whose anchoring to the posterior cortex requires long Osk. The anchoring of pole plasm components also requires actin cytoskeleton, and Osk promotes long F-actin projections in the oocyte posterior cytoplasm. However, the mechanism by which Osk mediates F-actin reorganization remains elusive. Furthermore, although long Osk is known to associate with endosomes under immuno-electron microscopy, it was not known whether this association is functionally significant. Here we show that Rabenosyn-5 (Rbsn-5), a Rab5 effector protein required for the early endocytic pathway, is crucial for pole plasm assembly. rbsn-5(-) oocytes fail to maintain microtubule polarity, which secondarily disrupts osk RNA localization. Nevertheless, anteriorly misexpressed Osk, particularly long Osk, recruits endosomal proteins, including Rbsn-5, and stimulates endocytosis. In oocytes lacking rbsn-5, the ectopic Osk induces aberrant F-actin aggregates, which diffuse into the cytoplasm along with pole plasm components. We propose that Osk stimulates endosomal cycling, which in turn promotes F-actin reorganization to anchor the pole plasm components to the oocyte cortex.

摘要

细胞命运通常由RNA和蛋白质的细胞内定位决定。在果蝇卵母细胞中,osk(oskar)RNA的定位以及随后在后极进行的Osk合成指导极质的组装,生殖系和腹部形成所需的因子在极质中积累。osk RNA产生两种异构体,即长Osk和短Osk,它们在极质组装中具有不同的功能。短Osk招募极质的下游成分,而这些成分锚定到后皮质需要长Osk。极质成分的锚定也需要肌动蛋白细胞骨架,并且Osk促进卵母细胞后细胞质中长的F-肌动蛋白突起。然而,Osk介导F-肌动蛋白重组的机制仍然不清楚。此外,尽管在免疫电子显微镜下已知长Osk与内体相关联,但尚不清楚这种关联在功能上是否重要。在这里,我们表明早期内吞途径所需的Rab5效应蛋白拉贝诺辛-5(Rbsn-5)对极质组装至关重要。rbsn-5(-)卵母细胞无法维持微管极性,进而破坏osk RNA的定位。尽管如此,在前部异位表达的Osk,特别是长Osk,会招募包括Rbsn-5在内的内体蛋白,并刺激内吞作用。在缺乏rbsn-5的卵母细胞中,异位的Osk会诱导异常的F-肌动蛋白聚集体,这些聚集体会与极质成分一起扩散到细胞质中。我们提出,Osk刺激内体循环,进而促进F-肌动蛋白重组,将极质成分锚定到卵母细胞皮质。

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