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Myc和SAGA在早期体细胞重编程过程中重塑了一个可变剪接网络。

Myc and SAGA rewire an alternative splicing network during early somatic cell reprogramming.

作者信息

Hirsch Calley L, Coban Akdemir Zeynep, Wang Li, Jayakumaran Gowtham, Trcka Dan, Weiss Alexander, Hernandez J Javier, Pan Qun, Han Hong, Xu Xueping, Xia Zheng, Salinger Andrew P, Wilson Marenda, Vizeacoumar Frederick, Datti Alessandro, Li Wei, Cooney Austin J, Barton Michelle C, Blencowe Benjamin J, Wrana Jeffrey L, Dent Sharon Y R

机构信息

Center for Systems Biology, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario M5G 1X5, Canada;

Program in Genes and Development, Graduate School of Biomedical Sciences, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA; Center for Cancer Epigenetics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA;

出版信息

Genes Dev. 2015 Apr 15;29(8):803-16. doi: 10.1101/gad.255109.114.

Abstract

Embryonic stem cells are maintained in a self-renewing and pluripotent state by multiple regulatory pathways. Pluripotent-specific transcriptional networks are sequentially reactivated as somatic cells reprogram to achieve pluripotency. How epigenetic regulators modulate this process and contribute to somatic cell reprogramming is not clear. Here we performed a functional RNAi screen to identify the earliest epigenetic regulators required for reprogramming. We identified components of the SAGA histone acetyltransferase complex, in particular Gcn5, as critical regulators of reprogramming initiation. Furthermore, we showed in mouse pluripotent stem cells that Gcn5 strongly associates with Myc and that, upon initiation of somatic reprogramming, Gcn5 and Myc form a positive feed-forward loop that activates a distinct alternative splicing network and the early acquisition of pluripotency-associated splicing events. These studies expose a Myc-SAGA pathway that drives expression of an essential alternative splicing regulatory network during somatic cell reprogramming.

摘要

胚胎干细胞通过多种调控途径维持自我更新和多能状态。当体细胞重编程以实现多能性时,多能特异性转录网络会被依次重新激活。表观遗传调节因子如何调节这一过程并促进体细胞重编程尚不清楚。在这里,我们进行了一项功能性RNAi筛选,以鉴定重编程所需的最早的表观遗传调节因子。我们确定了SAGA组蛋白乙酰转移酶复合物的成分,特别是Gcn5,是重编程起始的关键调节因子。此外,我们在小鼠多能干细胞中表明,Gcn5与Myc强烈相关,并且在体细胞重编程开始时,Gcn5和Myc形成一个正反馈前馈环,激活一个独特的可变剪接网络以及多能性相关剪接事件的早期获得。这些研究揭示了一条Myc-SAGA途径,该途径在体细胞重编程过程中驱动一个重要的可变剪接调节网络的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140b/4403257/87d088bdeb99/803f01.jpg

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