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Rrp6 被招募到转录基因,并伴随剪接的 mRNA 进入核孔。

Rrp6 is recruited to transcribed genes and accompanies the spliced mRNA to the nuclear pore.

机构信息

Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden.

出版信息

RNA. 2012 Aug;18(8):1466-74. doi: 10.1261/rna.032045.111. Epub 2012 Jun 28.

Abstract

Rrp6 is an exoribonuclease involved in the quality control of mRNA biogenesis. We have analyzed the association of Rrp6 with the Balbiani ring pre-mRNPs of Chironomus tentans to obtain insight into the role of Rrp6 in splicing surveillance. Rrp6 is recruited to transcribed genes and its distribution along the genes does not correlate with the positions of exons and introns. In the nucleoplasm, Rrp6 is bound to both unspliced and spliced transcripts. Rrp6 is released from the mRNPs in the vicinity of the nuclear pore before nucleo-cytoplasmic translocation. We show that Rrp6 is associated with newly synthesized transcripts during all the nuclear steps of gene expression and is associated with the transcripts independently of their splicing status. These observations suggest that the quality control of pre-mRNA splicing is not based on the selective recruitment of the exoribonuclease Rrp6 to unprocessed mRNAs.

摘要

Rrp6 是一种参与 mRNA 生物发生质量控制的外切核酸酶。我们分析了 Rrp6 与摇蚊 Balbiani 环前 mRNA 颗粒的关联,以深入了解 Rrp6 在剪接监测中的作用。Rrp6 被招募到转录基因上,其在基因上的分布与外显子和内含子的位置无关。在核质中,Rrp6 与未剪接和剪接的转录本结合。在核质转运之前,Rrp6 从核孔附近的 mRNP 中释放出来。我们表明,Rrp6 在基因表达的所有核步骤中都与新合成的转录本相关联,并且与转录本相关联,而与它们的剪接状态无关。这些观察结果表明,前体 mRNA 剪接的质量控制不是基于外切核酸酶 Rrp6 对未加工 mRNA 的选择性募集。

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