Département de Biochimie, Université de Montréal Montréal, Quebec H3C 3J7 Canada.
Genes Dev. 2010 Sep 1;24(17):1914-26. doi: 10.1101/gad.1937510. Epub 2010 Aug 16.
Pre-mRNA processing is coupled with transcription. It is still unclear if the transcription machinery can also directly affect the cytoplasmic fate of a transcript, such as its intracellular localization. In yeast, the RNA-binding protein She2p binds several mRNAs and targets them for localization at the bud. Here we report that She2p is recruited cotranscriptionally to the nascent bud-localized ASH1, IST2, and EAR1 mRNA. She2p interacts in vivo with the elongating forms of RNA polymerase II (pol II) via the transcription elongation factor Spt4-Spt5. Mutations in either SPT4 or SPT5 reduce the cotranscriptional recruitment of She2p on the ASH1 gene, disrupt the proper localization of ASH1 mRNA at the bud tip, and affect Ash1p sorting to the daughter cell nucleus. We propose that She2p is recruited by the RNA pol II machinery prior to its transfer to nascent bud-localized mRNAs. Indeed, She2p is present with RNA pol II on genes coding for localized or nonlocalized transcripts, but is associated with nascent mRNA only on genes coding for bud-localized transcripts. Moreover, a She2p mutant defective in RNA binding still associates with RNA pol II transcribed genes. This study uncovers a novel mechanism for the cotranscriptional assembly of mRNP complexes primed for localization in the cytoplasm.
前体 mRNA 处理与转录偶联。目前尚不清楚转录机制是否也可以直接影响转录本的细胞质命运,例如其在细胞内的定位。在酵母中,RNA 结合蛋白 She2p 结合多个 mRNA,并将其靶向定位于芽。在这里,我们报告说,She2p 在转录延伸因子 Spt4-Spt5 的作用下,与新生芽定位的 ASH1、IST2 和 EAR1 mRNA 共转录募集。在 SPT4 或 SPT5 中的突变会减少 She2p 在 ASH1 基因上的共转录募集,破坏 ASH1 mRNA 在芽尖的正确定位,并影响 Ash1p 向子细胞核的分拣。我们提出,She2p 在 RNA pol II 转移到新生成的芽定位 mRNA 之前被 RNA pol II 机制募集。事实上,She2p 存在于 RNA pol II 转录的基因编码的局部或非局部转录物上,但仅与编码芽定位转录物的基因上的新生 mRNA 相关联。此外,一个 RNA 结合缺陷的 She2p 突变体仍与 RNA pol II 转录的基因相关联。这项研究揭示了一种用于细胞质定位的 mRNP 复合物共转录组装的新机制。