Fortes Puri, Longman Dasa, McCracken Susan, Ip Joanna Y, Poot Raymond, Mattaj Iain W, Cáceres Javier F, Blencowe Benjamin J
Division of Gene Therapy and Hepatology, CIMA, University of Navarra, Pamplona, Spain.
FEBS Lett. 2007 Jun 26;581(16):3087-97. doi: 10.1016/j.febslet.2007.05.066. Epub 2007 Jun 4.
Precursor (pre)-mRNA splicing can impact the efficiency of coupled steps in gene expression. SRm160 (SR-related nuclear matrix protein of 160 kDa), is a splicing coactivator that also functions as a 3'-end cleavage-stimulatory factor. Here, we have identified an evolutionary-conserved SRm160-interacting protein, referred to as hRED120 (for human Arg/Glu/Asp-rich protein of 120 kDa). hRED120 contains a conventional RNA recognition motif and, like SRm160, a PWI nucleic acid binding domain, suggesting that it has the potential to bridge different RNP complexes. Also, similar to SRm160, hRED120 associates with snRNP components, and remains associated with mRNA after splicing. Simultaneous suppression in Caenorhabditis elegans of the ortholog of hRED120 with the orthologs of splicing and 3'-end processing factors results in aberrant growth or developmental defects. These results suggest that RED120 may function to couple splicing with mRNA 3'-end formation.
前体(pre)-mRNA剪接会影响基因表达中偶联步骤的效率。SRm160(160 kDa的SR相关核基质蛋白)是一种剪接共激活因子,也作为3'端切割刺激因子发挥作用。在此,我们鉴定出一种进化保守的与SRm160相互作用的蛋白,称为hRED120(人类120 kDa富含精氨酸/谷氨酸/天冬氨酸的蛋白)。hRED120含有一个传统的RNA识别基序,并且与SRm160一样,含有一个PWI核酸结合结构域,这表明它有潜力连接不同的核糖核蛋白复合体。此外,与SRm160相似,hRED120与snRNP组分相关联,并且在剪接后仍与mRNA相关联。在秀丽隐杆线虫中同时抑制hRED120的直系同源物与剪接和3'端加工因子的直系同源物会导致异常生长或发育缺陷。这些结果表明RED120可能起到将剪接与mRNA 3'端形成偶联的作用。