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通过体内系统 RNAi 筛选定义控制分化龛维持和功能的基因网络。

Defining gene networks controlling the maintenance and function of the differentiation niche by an in vivo systematic RNAi screen.

机构信息

PKU-THU Joint Center for Life Sciences, College of Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.

PKU-THU Joint Center for Life Sciences, College of Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China; Gene Regulatory Lab, School of Medicine, Tsinghua University, Beijing, 100084, China.

出版信息

J Genet Genomics. 2019 Jan 20;46(1):19-30. doi: 10.1016/j.jgg.2018.10.008. Epub 2019 Jan 30.

Abstract

In the Drosophila ovary, escort cells (ECs) extrinsically control germline stem cell (GSC) maintenance and progeny differentiation. However, the underlying mechanisms remain poorly understood. In this study, we identified 173 EC genes for their roles in controlling GSC maintenance and progeny differentiation by using an in vivo systematic RNAi approach. Of the identified genes, 10 and 163 are required in ECs to promote GSC maintenance and progeny differentiation, respectively. The genes required for progeny differentiation fall into different functional categories, including transcription, mRNA splicing, protein degradation, signal transduction and cytoskeleton regulation. In addition, the GSC progeny differentiation defects caused by defective ECs are often associated with BMP signaling elevation, indicating that preventing BMP signaling is a general functional feature of the differentiation niche. Lastly, exon junction complex (EJC) components, which are essential for mRNA splicing, are required in ECs to promote GSC progeny differentiation by maintaining ECs and preventing BMP signaling. Therefore, this study has identified the major regulators of the differentiation niche, which provides important insights into how stem cell progeny differentiation is extrinsically controlled.

摘要

在果蝇卵巢中,滋养细胞(ECs)通过外在机制控制生殖干细胞(GSCs)的维持和后代分化。然而,其潜在的机制仍知之甚少。在这项研究中,我们通过体内系统 RNAi 方法,鉴定了 173 个与调控 GSCs 维持和后代分化相关的 EC 基因。在鉴定的基因中,有 10 个和 163 个基因分别在 ECs 中促进 GSCs 的维持和后代分化是必需的。在与后代分化相关的基因中,有转录、mRNA 剪接、蛋白质降解、信号转导和细胞骨架调节等不同功能类别。此外,由于 EC 功能缺陷导致的 GSC 后代分化缺陷往往与 BMP 信号升高有关,这表明防止 BMP 信号是分化小生境的一个普遍功能特征。最后,对于 mRNA 剪接至关重要的外显子结合复合体(EJC)成分在 ECs 中也被需要,以通过维持 ECs 和防止 BMP 信号来促进 GSCs 后代分化。因此,本研究鉴定了分化小生境的主要调控因子,为理解干细胞后代分化如何受到外在控制提供了重要的见解。

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