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酿酒酵母中核外切体亚基Rrp6p缺失时不稳定的启动子相关转录本的积累。

Accumulation of unstable promoter-associated transcripts upon loss of the nuclear exosome subunit Rrp6p in Saccharomyces cerevisiae.

作者信息

Davis Carrie Anne, Ares Manuel

机构信息

Center for Molecular Biology of RNA, Department of Molecular, Cell, and Developmental Biology, Sinsheimer Laboratories, University of California, Santa Cruz, 95064, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Feb 28;103(9):3262-7. doi: 10.1073/pnas.0507783103. Epub 2006 Feb 16.

Abstract

Mutations in RRP6 result in the accumulation of aberrant polyadenylated transcripts from small nucleolar RNA genes. We exploited this observation to search for novel noncoding RNA genes in the yeast genome. When RNA from rrp6Delta yeast is compared with wild-type on whole-genome microarrays, numerous intergenic loci exhibit an increased mutant/wild type signal ratio. Among these loci, we found one encoding a new C/D box small nucleolar RNA, as well as a surprising number that gave rise to heterogeneous Trf4p-polyadenylated RNAs with lengths of approximately 250-500 nt. This class of RNAs is not easily detected in wild-type cells and appears associated with promoters. Fine mapping of several such transcripts shows they originate near known promoter elements but do not usually extend far enough to act as mRNAs, and may regulate the transcription of downstream mRNAs. Rather than being uninformative transcriptional "noise," we hypothesize that these transcripts reflect important features of RNA polymerase activity at the promoter. This activity is normally undetectable in wild-type cells because the transcripts are somehow distinguished from true mRNAs and are degraded in an Rrp6p-dependent fashion in the nucleus.

摘要

RRP6基因的突变导致小核仁RNA基因异常多聚腺苷酸化转录本的积累。我们利用这一观察结果在酵母基因组中寻找新的非编码RNA基因。当在全基因组微阵列上比较rrp6Delta酵母与野生型的RNA时,许多基因间位点显示出突变体/野生型信号比增加。在这些位点中,我们发现一个编码新的C/D盒小核仁RNA,还有数量惊人的位点产生了长度约为250 - 500 nt的异质Trf4p - 多聚腺苷酸化RNA。这类RNA在野生型细胞中不易检测到,且似乎与启动子相关。对几种此类转录本的精细定位表明,它们起源于已知启动子元件附近,但通常延伸不足够远以充当mRNA,并且可能调节下游mRNA的转录。我们推测这些转录本并非无信息的转录“噪音”,而是反映了启动子处RNA聚合酶活性的重要特征。这种活性在野生型细胞中通常无法检测到,因为这些转录本以某种方式与真正的mRNA区分开来,并在细胞核中以Rrp6p依赖的方式降解。

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