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由 GAGA 因子和 M1BP(一种新型转录因子)协调的转录暂停的独特机制。

Distinct mechanisms of transcriptional pausing orchestrated by GAGA factor and M1BP, a novel transcription factor.

机构信息

Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.

出版信息

EMBO J. 2013 Jul 3;32(13):1829-41. doi: 10.1038/emboj.2013.111. Epub 2013 May 24.

Abstract

Thousands of genes in Drosophila have Pol II paused in the promoter proximal region. Almost half of these genes are associated with either GAGA factor (GAF) or a newly discovered factor we call M1BP. Although both factors dictate the association of Pol II at their target promoters, they are nearly mutually exclusive on the genome and mediate different mechanisms of regulation. High-resolution mapping of Pol II using permanganate-ChIP-seq indicates that pausing on M1BP genes is transient and could involve the +1 nucleosome. In contrast, pausing on GAF genes is much stronger and largely independent of nucleosomes. Distinct regulatory mechanisms are reflected by transcriptional plasticity: M1BP genes are constitutively expressed throughout development while GAF genes exhibit much greater developmental specificity. M1BP binds a core promoter element called Motif 1. Motif 1 potentially directs a distinct transcriptional mechanism from the canonical TATA box, which does not correlate with paused Pol II on the genomic scale. In contrast to M1BP and GAF genes, a significant portion of TATA box genes appear to be controlled at preinitiation complex formation.

摘要

果蝇中的数千个基因在启动子近端区域有 Pol II 暂停。这些基因中几乎有一半与 GAGA 因子(GAF)或我们新发现的一种称为 M1BP 的因子有关。尽管这两种因子都决定了 Pol II 在其靶启动子上的结合,但它们在基因组上几乎是相互排斥的,并且介导不同的调控机制。使用高锰酸盐-ChIP-seq 对 Pol II 进行高分辨率作图表明,M1BP 基因上的暂停是短暂的,可能涉及 +1 核小体。相比之下,GAF 基因上的暂停要强得多,并且在很大程度上独立于核小体。不同的调控机制反映在转录可塑性上:M1BP 基因在整个发育过程中持续表达,而 GAF 基因表现出更大的发育特异性。M1BP 结合一个称为 Motif 1 的核心启动子元件。Motif 1 可能从经典的 TATA 盒指导一种不同的转录机制,这与基因组范围内暂停的 Pol II 不相关。与 M1BP 和 GAF 基因不同,相当一部分 TATA 盒基因似乎在起始前复合物形成时受到控制。

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