Bucheli Miriam E, He Xiaoyuan, Kaplan Craig D, Moore Claire L, Buratowski Stephen
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
RNA. 2007 Oct;13(10):1756-64. doi: 10.1261/rna.607207. Epub 2007 Aug 7.
Multiple steps in mRNA processing and transcription are coupled. Notably, the processing of mRNA 3' ends is linked to transcription termination by RNA polymerase II. Previously, we found that the yeast hnRNP protein Npl3 can negatively regulate 3' 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. Npl3 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 Npl3 with mRNA processing factors may promote recognition of proper polyadenylation sites while suppressing cryptic sites.
mRNA加工和转录过程中的多个步骤是相互关联的。值得注意的是,mRNA 3'末端的加工与RNA聚合酶II的转录终止相关联。此前,我们发现酵母hnRNP蛋白Npl3可以负向调节GAL1基因处的3'末端mRNA形成和终止。在此我们表明,CF IA聚腺苷酸化因子的Hrp1或Rna14亚基的过表达增加了对弱化聚腺苷酸化位点的识别。NPL3或HRP1的突变等位基因与RNA15的遗传相互作用也表明这些因子之间存在拮抗作用。Npl3与Rna15竞争结合聚腺苷酸化前体,并在体外抑制切割和聚腺苷酸化。这些结果表明,hnRNP蛋白的一个重要功能是确保mRNA加工的保真度。我们的结果支持一种模型,即Npl3与mRNA加工因子之间的平衡竞争可能促进对适当聚腺苷酸化位点的识别,同时抑制隐蔽位点。