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人类 cDNA 文库筛选揭示了两个与分化相关的基因 HHEX 和 HLX,它们作为早期重编程为多能性的启动子。

Screening of Human cDNA Library Reveals Two differentiation-Related Genes, HHEX and HLX, as Promoters of Early Phase Reprogramming toward Pluripotency.

机构信息

Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.

Japan Biological Informatics Consortium, Tokyo, Japan.

出版信息

Stem Cells. 2016 Nov;34(11):2661-2669. doi: 10.1002/stem.2436. Epub 2016 Jul 8.

Abstract

Gene screenings have identified a number of reprogramming factors that induce pluripotency from somatic cells. However, the screening methods have mostly considered only factors that maintain pluripotency in embryonic stem cells, ignoring a potentially long list of other contributing factors involved. To expand the search, we developed a new screening method that examined 2,008 human genes in the generation of human induced pluripotent stem cells (iPSCs), including not only pluripotent genes but also differentiation-related genes that suppress pluripotency. We found the top 100 genes that increased reprogramming efficiency and discovered they contained many differentiation-related genes and homeobox genes. We selected two, HHEX and HLX, for further analysis. These genes enhanced the appearance of premature reprograming cells in the early phase of human iPSC induction, but had inhibitory effect on the late phase. In addition, when expressed in human iPSCs, HHEX and HLX interfered with the pluripotent state, indicating inverse effects on somatic reprograming and pluripotent maintenance. These results demonstrate that our screening is useful for identifying differentiation-related genes in somatic reprograming. Stem Cells 2016;34:2661-2669.

摘要

基因筛查已经鉴定出许多重编程因子,可以将体细胞诱导为多能性。然而,这些筛选方法大多只考虑了维持胚胎干细胞多能性的因子,而忽略了潜在的许多其他参与的因子。为了扩大搜索范围,我们开发了一种新的筛选方法,用于在人类诱导多能干细胞(iPSC)的生成中检查 2008 个人类基因,包括不仅是多能性基因,还有抑制多能性的分化相关基因。我们发现了提高重编程效率的前 100 个基因,并发现它们包含许多分化相关基因和同源盒基因。我们选择了两个基因,HHEX 和 HLX,进行进一步分析。这些基因在人类 iPSC 诱导的早期阶段增强了早期重编程细胞的出现,但对后期具有抑制作用。此外,当在人类 iPSC 中表达时,HHEX 和 HLX 干扰了多能状态,表明对体细胞重编程和多能性维持具有相反的影响。这些结果表明,我们的筛选方法可用于鉴定体细胞重编程中的分化相关基因。《干细胞》2016 年;34:2661-2669.

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