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抑制 DNA 结合:ncRNAs 和蛋白结构域转录抑制的共同机制。

Dampening DNA binding: a common mechanism of transcriptional repression for both ncRNAs and protein domains.

机构信息

Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO, USA.

出版信息

RNA Biol. 2010 May-Jun;7(3):305-9. doi: 10.4161/rna.7.3.11910. Epub 2010 May 26.

Abstract

With eukaryotic non-coding RNAs (ncRNAs) now established as critical regulators of cellular transcription, the true diversity with which they can elicit biological effects is beginning to be appreciated. Two ncRNAs, mouse B2 RNA and human Alu RNA, have been found to repress mRNA transcription in response to heat shock. They do so by binding directly to RNA polymerase II, assembling into complexes on promoter DNA, and disrupting contacts between the polymerase and the DNA. Such a mechanism of repression had not previously been observed for a eukaryotic ncRNA; however, there are examples of eukaryotic protein domains that repress transcription by blocking essential protein-DNA interactions. Comparing the mechanism of transcriptional repression utilized by these protein domains to that used by B2 and Alu RNAs raises intriguing questions regarding transcriptional control, and how B2 and Alu RNAs might themselves be regulated.

摘要

真核非编码 RNA(ncRNA)已被确定为细胞转录的关键调节剂,其能够引发生物学效应的真正多样性开始被人们所认识。两种 ncRNA,小鼠 B2 RNA 和人类 Alu RNA,已被发现可以在热休克时抑制 mRNA 转录。它们通过直接与 RNA 聚合酶 II 结合,在启动子 DNA 上组装成复合物,并破坏聚合酶与 DNA 之间的接触来实现这一点。这种抑制机制以前在真核 ncRNA 中没有观察到;然而,有一些真核蛋白结构域的例子通过阻断必需的蛋白-DNA 相互作用来抑制转录。将这些蛋白结构域所利用的转录抑制机制与 B2 和 Alu RNA 所利用的机制进行比较,引发了关于转录控制的有趣问题,以及 B2 和 Alu RNA 本身如何被调控。

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