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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Myc and SAGA rewire an alternative splicing network during early somatic cell reprogramming
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Myc and SAGA rewire an alternative splicing network during early somatic cell reprogramming

机译:Myc和SAGA在早期的体细胞重编程过程中重新布线了另一种剪接网络

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摘要

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. Weidentified components of the SAGA histone acetyltransferase complex, in particular Gcn5, as critical regulators of reprogramming initiation. Furthermore, we showed in mouse pluripotent stemcells 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.
机译:胚胎干细胞通过多种调节途径维持在自我更新和多能的状态。当体细胞重编程以实现多能性时,多能性特异性转录网络被顺序地重新激活。表观遗传调节物如何调节这一过程并促进体细胞重编程尚不清楚。在这里,我们进行了功能性RNAi筛选,以识别重编程所需的最早的表观遗传调控因子。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剂。此外,我们在小鼠多能干细胞中显示Gcn5与Myc密切相关,并且在体细胞重编程启动后,Gcn5和Myc形成正向前馈环,该环激活了独特的替代剪接网络并与多能性相关的剪接事件得以早期获得。 。这些研究揭示了Myc-SAGA途径,该途径在体细胞重编程过程中驱动必需的替代剪接调控网络的表达。

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