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核外切体复合物有助于对NAB2信使核糖核酸水平进行自身调控。

The nuclear exosome contributes to autogenous control of NAB2 mRNA levels.

作者信息

Roth Kelly M, Wolf Maria K, Rossi Marie, Butler J Scott

机构信息

Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Box 672, 601 Elmwood Ave., Rochester, NY 14642, USA.

出版信息

Mol Cell Biol. 2005 Mar;25(5):1577-85. doi: 10.1128/MCB.25.5.1577-1585.2005.

Abstract

The RNA-processing exosome is a complex of riboexonucleases required for 3'-end formation of some noncoding RNAs and for the degradation of mRNAs in eukaryotes. The nuclear form of the exosome functions in an mRNA surveillance pathway that retains and degrades improperly processed precursor mRNAs within the nucleus. We report here that the nuclear exosome controls the level of NAB2 mRNA, encoding the nuclear poly(A)+-RNA-binding protein Nab2p. Mutations affecting the activity of the nuclear, but not the cytoplasmic, exosome cause an increase in the amount of NAB2 mRNA. Cis- and trans-acting mutations that inhibit degradation by the nuclear-exosome subunit Rrp6p result in elevated levels of NAB2 mRNA. Control of NAB2 mRNA levels occurs posttranscriptionally and requires a sequence of 26 consecutive adenosines (A26) in the NAB2 3' untranslated region, which represses NAB2 3'-end formation and sensitizes the transcript to degradation by Rrp6p. Analysis of NAB2 mRNA levels in a nab2-1 mutant and in the presence of excess Nab2p indicates that Nab2p activity negatively controls NAB2 mRNA levels in an A26- and Rrp6p-dependent manner. These findings suggest a novel regulatory circuit in which the nuclear exosome controls the level of NAB2 mRNA in response to changes in the activity of Nab2 protein.

摘要

RNA 加工外切体是一种核糖核酸外切酶复合物,在真核生物中,它对于某些非编码 RNA 的 3' 末端形成以及 mRNA 的降解是必需的。外切体的核形式在一种 mRNA 监测途径中发挥作用,该途径可保留并降解细胞核内加工不当的前体 mRNA。我们在此报告,核外切体控制着编码核 poly(A)+RNA 结合蛋白 Nab2p 的 NAB2 mRNA 的水平。影响核外切体而非胞质外切体活性的突变会导致 NAB2 mRNA 量的增加。抑制核外切体亚基 Rrp6p 介导的降解的顺式和反式作用突变会导致 NAB2 mRNA 水平升高。NAB2 mRNA 水平的控制发生在转录后,并且需要 NAB2 3' 非翻译区中一段连续的 26 个腺苷(A26)序列,该序列会抑制 NAB2 的 3' 末端形成,并使转录本对 Rrp6p 介导的降解敏感。对 nab2-1 突变体以及在存在过量 Nab2p 情况下的 NAB2 mRNA 水平分析表明,Nab2p 活性以 A26 和 Rrp6p 依赖的方式负调控 NAB2 mRNA 水平。这些发现提示了一种新的调控回路,其中核外切体响应 Nab2 蛋白活性的变化来控制 NAB2 mRNA 的水平。

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