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Drosophila Squid/hnRNP helps Dynein switch from a gurken mRNA transport motor to an ultrastructural static anchor in sponge bodies.

机译:果蝇鱿鱼/ hnRNP帮助Dynein从海绵状mRNA的转运蛋白转运蛋白转变为超微结构静态锚。

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摘要

In Drosophila oocytes, dorso-anterior transport of gurken mRNA requires both the Dynein motor and the heterogeneous nuclear ribonucleoprotein (hnRNP) Squid. We show that gurken transcripts are transported directly on microtubules by Dynein in nonmembranous electron-dense transport particles that also contain Squid and the transport cofactors Egalitarian and Bicaudal-D. At its destination, gurken mRNA is statically anchored by Dynein within large electron-dense cytoplasmic structures known as sponge bodies. Egalitarian and Bicaudal-D contribute only to active transport, whereas Dynein and Squid are also required for gurken mRNA anchoring and the integrity of sponge bodies. Disrupting Dynein function disperses gurken mRNA homogeneously throughout the cytoplasm, whereas the loss of Squid function converts the sponge bodies into active transport particles. We propose that Dynein acts as a static structural component for the assembly of gurken mRNA transport and anchoring complexes, and that Squid is required for the dynamic conversion of transport particles to sponge bodies.
机译:在果蝇卵母细胞中,古尔肯mRNA的背侧向前运输既需要Dynein运动,也需要异质核核糖核蛋白(hnRNP)鱿鱼。我们显示,在非膜电子致密的运输颗粒,其中也包含鱿鱼和运输辅因子Egalitarian和Bicaudal-D的Dynein直接在微管上运输Gurken成绩单。在其目的地,古尔肯mRNA被Dynein静态锚定在被称为海绵体的大型电子密集细胞质结构中。 Egalitarian和Bicaudal-D仅有助于主动转运,而Dynein和Squid也需要用于刺突的mRNA锚定和海绵体的完整性。破坏性的Dynein功能使古兰经的mRNA均匀地分散在整个细胞质中,而鱿鱼功能的丧失则将海绵体转化为活性转运颗粒。我们建议,Dynein充当古肯mRNA运输和锚固复合物装配的静态结构成分,并且Squid是运输颗粒向海绵体动态转化所必需的。

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