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7SK snRNA-mediated, gene-specific cooperativity of HMGA1 and P-TEFb

机译:7SK snRNA介导的HMGA1和P-TEFb的基因特异性协同作用

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摘要

7SK small-nuclear RNA has been shown to negatively regulate P-TEFb transcription elongation on the one hand and control HMGA1 transcription initiation and chromatin remodeling on the other. The non-coding 7SK RNA thereby directly interacts with both factors through different regions. While the loop 2 of the RNA specifically binds to the first HMGA1 A/T hook, thereby competing with DNA binding to the same domain, loops 1, 3 and 4 are involved in P-TEFb interaction. This raises the question of whether HMGA1 and P-TEFb cooperate during gene transcription. Using transcriptome profiling, we have identifed genes that are oppositely regulated by 7SK RNA overexpression versus shRNA mediated knockdown. Inhibition of P-TEFb by competitive expression of a dominant-negative Cdk9 protein leads to highly similar changes in global gene expression as the overexpression of 7SK RNA, confirming the importance of P-TEFb inhibition by 7SK RNA. Furthermore, we have similarly assembled genes affected concomitantly by HMGA1 overexpression. HMGA1 and P-TEFb, in the case of select target genes, show strong cooperation in transcriptional activation. Finally, we provide evidence for 7SK RNA complexes containing simultaneously HMGA1 and P-TEFb. 7SK RNA thus establishes gene-dependent plasticity between HMGA1 chromatin remodeling and transcription initiation and P-TEFb transcription elongation.
机译:已显示7SK小核RNA一方面负调控P-TEFb转录伸长,另一方面控制HMGA1转录起始和染色质重塑。因此,非编码7SK RNA通过不同区域直接与两个因子相互作用。尽管RNA的环2与第一个HMGA1 A / T钩特异性结合,从而与与相同结构域结合的DNA竞争,但环1、3和4参与了P-TEFb相互作用。这就提出了在基因转录过程中HMGA1和P-TEFb是否协同作用的问题。使用转录组分析,我们已经鉴定出与7shRNA介导的敲低相反,其受7SK RNA过表达相反调控的基因。通过显性阴性Cdk9蛋白的竞争性表达抑制P-TEFb导致了全球基因表达的高度相似,这与7SK RNA的过表达相似,从而证实了7SK RNA抑制P-TEFb的重要性。此外,我们有类似组装的基因同时受到HMGA1过表达的影响。在选择目标基因的情况下,HMGA1和P-TEFb在转录激活中显示出强大的合作性。最后,我们为同时包含HMGA1和P-TEFb的7SK RNA复合物提供了证据。因此,7SK RNA在HMGA1染色质重塑和转录起始与P-TEFb转录延伸之间建立了基因依赖性可塑性。

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