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全基因组RNA干扰筛选鉴定出参与果蝇肠道干细胞调控的网络。

Genome-wide RNAi screen identifies networks involved in intestinal stem cell regulation in Drosophila.

作者信息

Zeng Xiankun, Han Lili, Singh Shree Ram, Liu Hanhan, Neumüller Ralph A, Yan Dong, Hu Yanhui, Liu Ying, Liu Wei, Lin Xinhua, Hou Steven X

机构信息

Basic Research Laboratory, National Cancer Institute at Frederick, NIH, Frederick, MD 21702, USA.

Key Laboratory of Stem Cell and Developmental Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100864, China.

出版信息

Cell Rep. 2015 Feb 24;10(7):1226-38. doi: 10.1016/j.celrep.2015.01.051. Epub 2015 Feb 19.

Abstract

The intestinal epithelium is the most rapidly self-renewing tissue in adult animals and maintained by intestinal stem cells (ISCs) in both Drosophila and mammals. To comprehensively identify genes and pathways that regulate ISC fates, we performed a genome-wide transgenic RNAi screen in adult Drosophila intestine and identified 405 genes that regulate ISC maintenance and lineage-specific differentiation. By integrating these genes into publicly available interaction databases, we further developed functional networks that regulate ISC self-renewal, ISC proliferation, ISC maintenance of diploid status, ISC survival, ISC-to-enterocyte (EC) lineage differentiation, and ISC-to-enteroendocrine (EE) lineage differentiation. By comparing regulators among ISCs, female germline stem cells, and neural stem cells, we found that factors related to basic stem cell cellular processes are commonly required in all stem cells, and stem-cell-specific, niche-related signals are required only in the unique stem cell type. Our findings provide valuable insights into stem cell maintenance and lineage-specific differentiation.

摘要

肠道上皮是成年动物中自我更新最快的组织,在果蝇和哺乳动物中均由肠道干细胞(ISC)维持。为了全面鉴定调控ISC命运的基因和通路,我们在成年果蝇肠道中进行了全基因组转基因RNA干扰筛选,鉴定出405个调控ISC维持和谱系特异性分化的基因。通过将这些基因整合到公开的相互作用数据库中,我们进一步构建了调控ISC自我更新、ISC增殖、ISC二倍体状态维持、ISC存活、ISC向肠上皮细胞(EC)谱系分化以及ISC向肠内分泌细胞(EE)谱系分化的功能网络。通过比较ISC、雌性生殖系干细胞和神经干细胞中的调控因子,我们发现与基本干细胞细胞过程相关的因子在所有干细胞中普遍需要,而干细胞特异性的、与生态位相关的信号仅在独特的干细胞类型中需要。我们的研究结果为干细胞维持和谱系特异性分化提供了有价值的见解。

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