Noé Griselda, De Gaudenzi Javier G, Frasch Alberto C
Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico Chascomús, UNSAM-CONICET, Av, Gral, Paz 5445, INTI, Edificio 24, 1650 San Martín, Provincia de Buenos Aires, Argentina.
BMC Mol Biol. 2008 Dec 8;9:107. doi: 10.1186/1471-2199-9-107.
Trypanosomes mostly control gene expression by post-transcriptional events such as modulation of mRNA stability and translational efficiency. These mechanisms involve RNA-binding proteins (RBPs), which associate with transcripts to form messenger ribonucleoprotein (mRNP) complexes.
In this study, we report the identification of mRNA targets for Trypanosoma cruzi U-rich RBP 1 (TcUBP1) and T. cruzi RBP 3 (TcRBP3), two phylogenetically conserved proteins among Kinetoplastids. Co-immunoprecipitated RBP-associated RNAs were extracted from mRNP complexes and binding of RBPs to several targets was confirmed by independent experimental assays. Analysis of target transcript sequences allowed the identification of different signature RNA motifs for each protein. Cis-elements for RBP binding have a stem-loop structure of 30-35 bases and are more frequently represented in the 3'-untranslated region (UTR) of mRNAs. Insertion of the correctly folded RNA elements to a non-specific mRNA rendered it into a target transcript, whereas substitution of the RNA elements abolished RBP interaction. In addition, RBPs competed for RNA-binding sites in accordance with the distribution of different and overlapping motifs in the 3'-UTRs of common mRNAs.
Functionally related transcripts were preferentially associated with a given RBP; TcUBP1 targets were enriched in genes encoding proteins involved in metabolism, whereas ribosomal protein-encoding transcripts were the largest group within TcRBP3 targets. Together, these results suggest coordinated control of different mRNA subsets at the post-transcriptional level by specific RBPs.
锥虫大多通过转录后事件来控制基因表达,如调节mRNA稳定性和翻译效率。这些机制涉及RNA结合蛋白(RBP),其与转录本结合形成信使核糖核蛋白(mRNP)复合物。
在本研究中,我们报告了对克氏锥虫富含尿嘧啶的RBP 1(TcUBP1)和克氏锥虫RBP 3(TcRBP3)的mRNA靶标的鉴定,这两种蛋白是动质体中系统发育保守的蛋白。从mRNP复合物中提取共免疫沉淀的RBP相关RNA,并通过独立实验分析确认RBP与多个靶标的结合。对靶标转录本序列的分析使得能够鉴定每种蛋白的不同特征RNA基序。RBP结合的顺式元件具有30 - 35个碱基的茎环结构,且在mRNA的3'非翻译区(UTR)中更频繁出现。将正确折叠的RNA元件插入非特异性mRNA使其成为靶标转录本,而RNA元件的替换则消除了RBP相互作用。此外,根据常见mRNA的3' - UTR中不同和重叠基序的分布,RBPs竞争RNA结合位点。
功能相关的转录本优先与特定RBP结合;TcUBP1的靶标在编码参与代谢的蛋白质的基因中富集,而编码核糖体蛋白的转录本是TcRBP3靶标中最大的一组。总之,这些结果表明特定RBP在转录后水平对不同mRNA亚群进行协调控制。