Hage Rosemary, Tung Luh, Du Hansen, Stands Leah, Rosbash Michael, Chang Tien-Hsien
Department of Molecular Genetics, The Ohio State University, 484 West 12th Ave., Columbus, OH 43210, USA.
Mol Cell Biol. 2009 Jul;29(14):3941-52. doi: 10.1128/MCB.00384-09. Epub 2009 May 18.
To understand how DEXD/H-box proteins recognize and interact with their cellular substrates, we have been studying Prp28p, a DEXD/H-box splicing factor required for switching the U1 snRNP with the U6 snRNP at the precursor mRNA (pre-mRNA) 5' splice site. We previously demonstrated that the requirement for Prp28p can be eliminated by mutations that alter either the U1 snRNA or the U1C protein, suggesting that both are targets of Prp28p. Inspired by this finding, we designed a bypass genetic screen to specifically search for additional, novel targets of Prp28p. The screen identified Prp42p, Snu71p, and Cbp80p, all known components of commitment complexes, as well as Ynl187p, a protein of uncertain function. To examine the role of Ynl187p in splicing, we carried out extensive genetic and biochemical analysis, including chromatin immunoprecipitation. Our data suggest that Ynl187p acts in concert with U1C and Cbp80p to help stabilize the U1 snRNP-5' splice site interaction. These findings are discussed in the context of DEXD/H-box proteins and their role in vivo as well as the potential need for more integral U1-snRNP proteins in governing the fungal 5' splice site RNA-RNA interaction compared to the number of U1 snRNP proteins needed by metazoans.
为了了解DEXD/H-box蛋白如何识别其细胞底物并与之相互作用,我们一直在研究Prp28p,它是一种DEXD/H-box剪接因子,在前体mRNA(pre-mRNA)的5'剪接位点参与U1 snRNP与U6 snRNP的转换。我们之前证明,改变U1 snRNA或U1C蛋白的突变可以消除对Prp28p的需求,这表明两者都是Prp28p的作用靶点。受这一发现的启发,我们设计了一个旁路遗传筛选,专门寻找Prp28p的其他新靶点。筛选鉴定出Prp42p、Snu71p和Cbp80p,它们都是剪接前体复合物的已知组分,以及功能未知的Ynl187p蛋白。为了研究Ynl187p在剪接中的作用,我们进行了广泛的遗传和生化分析,包括染色质免疫沉淀。我们的数据表明,Ynl187p与U1C和Cbp80p协同作用,有助于稳定U1 snRNP-5'剪接位点的相互作用。我们将在DEXD/H-box蛋白及其在体内的作用背景下讨论这些发现,以及与后生动物所需的U1 snRNP蛋白数量相比,在控制真菌5'剪接位点RNA-RNA相互作用方面可能需要更多完整的U1-snRNP蛋白。