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果蝇细胞化过程中slam的定位与翻译控制

Localization and translation control of slam in Drosophila cellularization.

作者信息

Yan Shuling, Großhans Jörg

机构信息

a Institute for Developmental Biochemistry, Medical School , University of Göttingen , Göttingen , Germany.

出版信息

Fly (Austin). 2018;12(3-4):191-198. doi: 10.1080/19336934.2018.1520574. Epub 2018 Sep 18.

DOI:10.1080/19336934.2018.1520574
PMID:30211628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6988885/
Abstract

In this extra view, we comment on our recent work concerning the mRNA localization of the gene slow as molasses (slam). slam is a gene essential for the polarized invagination of the plasma membrane and separation of basal and lateral cortical domains during cellularization as well as for germ cell migration in later embryogenesis. We have demonstrated an intimate relationship between slam RNA and its encoded protein. Slam RNA co-localizes and forms a complex with its encoded protein. Slam mRNA localization not only is required for reaching full levels of functional Slam protein but also depends on Slam protein. The translation of slam mRNA is subject to tight spatio-temporal regulation leading to a rapid accumulation of Slam protein and zygotic slam RNA at the furrow canal. In this extra view, we first discuss the mechanism controlling localization and translation of slam RNA. In addition, we document in detail the maternal and zygotic expression of slam RNA and protein and provide data for a function in membrane stabilization. Furthermore, we mapped the region of Slam protein mediating cortical localization in cultured cells.

摘要

在这篇补充观点文章中,我们对近期关于“慢如糖浆”(slam)基因的mRNA定位的研究工作进行评论。slam基因对于细胞膜的极化内陷以及细胞化过程中基底和侧面皮质结构域的分离,以及后期胚胎发育中的生殖细胞迁移至关重要。我们已经证明了slam RNA与其编码蛋白之间存在密切关系。slam RNA与其编码蛋白共定位并形成复合物。slam mRNA定位不仅是达到功能完整水平的Slam蛋白所必需的,而且还依赖于Slam蛋白。slam mRNA的翻译受到严格的时空调控,导致Slam蛋白和合子型slam RNA在沟道处快速积累。在这篇补充观点文章中,我们首先讨论控制slam RNA定位和翻译的机制。此外,我们详细记录了slam RNA和蛋白的母体和合子型表达,并提供了其在膜稳定中的功能数据。此外,我们绘制了在培养细胞中介导皮质定位的Slam蛋白区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/02826e0f6156/kfly-12-3-4-1520574-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/ddf4c2768ca5/kfly-12-3-4-1520574-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/eecd94d03f76/kfly-12-3-4-1520574-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/02826e0f6156/kfly-12-3-4-1520574-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/ddf4c2768ca5/kfly-12-3-4-1520574-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/eecd94d03f76/kfly-12-3-4-1520574-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8999/6988885/02826e0f6156/kfly-12-3-4-1520574-g003.jpg

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ME31B globally represses maternal mRNAs by two distinct mechanisms during the maternal-to-zygotic transition.ME31B 在母胎向合子的过渡过程中通过两种不同的机制全局抑制母体 mRNA。
Elife. 2017 Sep 6;6:e27891. doi: 10.7554/eLife.27891.
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Translational repression of the mRNA involves the RNA helicase Belle and RNA coating by Me31B and Trailer hitch.mRNA的翻译抑制涉及RNA解旋酶Belle以及Me31B和Trailer hitch对RNA的包被。
RNA. 2017 Oct;23(10):1552-1568. doi: 10.1261/rna.062208.117. Epub 2017 Jul 12.
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