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RNA target specificity of the STAR/GSG domain post-transcriptional regulatory protein GLD-1

机译:STAR / GSG域转录后调控蛋白GLD-1的RNA靶标特异性

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摘要

The post-transcriptional regulation of gene expression underlies several critical developmental phenomena. In metazoa, gene products that are expressed, silenced and packaged during oogenesis govern early developmental processes prior to nascent transcription activation. Furthermore, tissue-specific alternative splicing of several transcription factors controls pattern formation and organ development. A highly conserved family of proteins containing a STAR/GSG RNA-binding domain is essential to both processes. Here, we identify the consensus STAR-binding element (SBE) required for specific mRNA recognition by GLD-1, a key regulator of Caenorhabditis elegans germline development. We have identified and verified new GLD-1 repression targets containing this sequence. The results suggest additional functions of GLD-1 in X-chromosome silencing and early embryogenesis. The SBE is present in Quaking and How mRNA targets, suggesting that STAR protein specificity is highly conserved. Similarities between the SBE and the branch-site signal indicate a possible competition mechanism for STAR/GSG regulation of splicing variants.
机译:基因表达的转录后调控是几种关键的发育现象的基础。在后生动物中,在卵子发生过程中表达,沉默和包装的基因产物控制着新生的转录激活之前的早期发育过程。此外,几个转录因子的组织特异性替代剪接控制模式形成和器官发育。包含STAR / GSG RNA结合结构域的高度保守的蛋白质家族对于这两个过程都是必不可少的。在这里,我们确定了秀丽隐杆线虫种系发育的关键调节剂GLD-1识别特定mRNA所需的共有STAR结合元件(SBE)。我们已经鉴定并验证了包含该序列的新GLD-1抑制靶标。结果表明GLD-1在X染色体沉默和早期胚胎发生中的其他功能。 SBE存在于Quaking和How mRNA靶标中,表明STAR蛋白特异性高度保守。 SBE和分支站点信号之间的相似性表明可能有竞争机制对STAR / GSG剪接变体进行调控。

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