Kiesler Eva, Hase Manuela E, Brodin David, Visa Neus
Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden.
J Cell Biol. 2005 Mar 28;168(7):1013-25. doi: 10.1083/jcb.200407173. Epub 2005 Mar 21.
Here, we study an insect hnRNP M protein, referred to as Hrp59. Hrp59 is relatively abundant, has a modular domain organization containing three RNA-binding domains, is dynamically recruited to transcribed genes, and binds to premRNA cotranscriptionally. Using the Balbiani ring system of Chironomus, we show that Hrp59 accompanies the mRNA from the gene to the nuclear envelope, and is released from the mRNA at the nuclear pore. The association of Hrp59 with transcribed genes is not proportional to the amount of synthesized RNA, and in vivo Hrp59 binds preferentially to a subset of mRNAs, including its own mRNA. By coimmunoprecipitation of Hrp59-RNA complexes and microarray hybridization against Drosophila whole-genome arrays, we identify the preferred mRNA targets of Hrp59 in vivo and show that Hrp59 is required for the expression of these target mRNAs. We also show that Hrp59 binds preferentially to exonic splicing enhancers and our results provide new insights into the role of hnRNP M in splicing regulation.
在此,我们研究一种昆虫的hnRNP M蛋白,称为Hrp59。Hrp59相对丰富,具有包含三个RNA结合结构域的模块化结构域组织,动态募集到转录基因上,并在转录前体mRNA共转录时与之结合。利用摇蚊的巴尔比亚尼环系统,我们发现Hrp59伴随mRNA从基因转运至核膜,并在核孔处从mRNA上释放。Hrp59与转录基因的结合并不与合成RNA的量成比例,且在体内Hrp59优先结合一部分mRNA,包括其自身的mRNA。通过对Hrp59-RNA复合物进行共免疫沉淀以及针对果蝇全基因组阵列进行微阵列杂交,我们确定了Hrp59在体内的优先mRNA靶标,并表明这些靶标mRNA的表达需要Hrp59。我们还表明Hrp59优先结合外显子剪接增强子,我们的结果为hnRNP M在剪接调控中的作用提供了新的见解。