Polyadenylation site choice in yeast is affected by competition between Npl3 and polyadenylation factor CFI

被引:43
作者
Bucheli, Miriam E.
He, Xiaoyuan
Kaplan, Craig D.
Moore, Claire L.
Buratowski, Stephen
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Mol Microbiol, Boston, MA 02115 USA
[3] Stanford Univ, Dept Biol Struct, Stanford, CA 94305 USA
关键词
mRNA 39 end processing; transcription termination; cleavage; polyadenylation;
D O I
10.1261/rna.607207
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multiple steps in mRNA processing and transcription are coupled. Notably, the processing of mRNA 39 ends is linked to transcription termination by RNA polymerase II. Previously, we found that the yeast hnRNP protein NpI3 can negatively regulate 39 end mRNA formation and termination at the GAL1 gene. Here we show that overexpression of the Hrp1 or Rna14 subunits of the CF IA polyadenylation factor increases recognition of a weakened polyadenylation site. Genetic interactions of mutant alleles of NPL3 or HRP1 with RNA15 also indicate antagonism between these factors. NpI3 competes with Rna15 for binding to a polyadenylation precursor and inhibits cleavage and polyadenylation in vitro. These results suggest that an important function of hnRNP proteins is to ensure the fidelity of mRNA processing. Our results support a model in which balanced competition of NpI3 with mRNA processing factors may promote recognition of proper polyadenylation sites while suppressing cryptic sites.
引用
收藏
页码:1756 / 1764
页数:9
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