Messenger RNAs are recruited for nuclear export during transcription

被引:187
作者
Lei, EP
Krebber, H
Silver, PA [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
transcription; mRNA export; chromatin IP; RNA polymerase II; Npl3; Yra1;
D O I
10.1101/gad.892401
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
following transcription and processing, eukaryotic mRNAs are exported from the nucleus to the cytoplasm for translation. Here we present evidence that mRNAs are targeted for nuclear export cotranscriptionally. Combined mutations in the Saccharomyces cerevisiae hnRNP Npl3 and TATA-binding protein (TBP) block mRNA export, implying that cotranscriptional recruitment of Npl3 is required for efficient export of mRNA. furthermore, Npl3 can be found in a complex with RNA Pol II, indicating that Npl3 associates with the transcription machinery. Finally, Npl3 is recruited to genes in a transcription dependent manner as determined by chromatin immunoprecipitation. Another mRNA export factor, Yra1, also associates with chromatin cotranscriptionally but appears to be recruited at a later step. Taken together, our results suggest that export factors are recruited to the sites of transcription to promote efficient mRNA export.
引用
收藏
页码:1771 / 1782
页数:12
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