Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235, USA.
Development. 2011 May;138(9):1817-26. doi: 10.1242/dev.056697. Epub 2011 Mar 29.
microRNAs (miRNAs) are a family of 21-23 nucleotide endogenous non-coding RNAs that post-transcriptionally regulate gene expression in a sequence-specific manner. Typically, miRNAs downregulate target genes by recognizing and recruiting protein complexes to 3'UTRs, followed by translation repression or mRNA degradation. miR-92 is a well-studied oncogene in mammalian systems. Here, using zebrafish as a model system, we uncovered a novel tissue-inductive role for miR-92 during early vertebrate development. Overexpression resulted in reduced endoderm formation during gastrulation with consequent cardia and viscera bifida. By contrast, depletion of miR-92 increased endoderm formation, which led to abnormal Kupffer's vesicle development and left-right patterning defects. Using target prediction algorithms and reporter constructs, we show that gata5 is a target of miR-92. Alteration of gata5 levels reciprocally mirrored the effects of gain and loss of function of miR-92. Moreover, genetic epistasis experiments showed that miR-92-mediated defects could be substantially suppressed by modulating gata5 levels. We propose that miR-92 is a critical regulator of endoderm formation and left-right asymmetry during early zebrafish development and provide the first evidence for a regulatory function for gata5 in the formation of Kupffer's vesicle and left-right patterning.
微小 RNA(miRNAs)是一类 21-23 个核苷酸的内源性非编码 RNA,以序列特异性方式在后转录水平调节基因表达。通常,miRNAs 通过识别和招募蛋白复合物到 3'UTR 来下调靶基因,随后抑制翻译或 mRNA 降解。miR-92 是哺乳动物系统中研究得很好的致癌基因。在这里,我们使用斑马鱼作为模型系统,揭示了 miR-92 在早期脊椎动物发育过程中的一个新的组织诱导作用。过表达导致原肠胚形成期间内胚层形成减少,从而导致心脏和内脏二分。相比之下,miR-92 的耗尽增加了内胚层的形成,导致异常的 Kupffer 囊泡发育和左右模式缺陷。通过靶基因预测算法和报告基因构建,我们表明 gata5 是 miR-92 的靶基因。gata5 水平的改变与 miR-92 功能获得和缺失的作用呈反向对应关系。此外,遗传上位性实验表明,通过调节 gata5 水平可以显著抑制 miR-92 介导的缺陷。我们提出,miR-92 是早期斑马鱼发育过程中内胚层形成和左右不对称的关键调节因子,并为 gata5 在 Kupffer 囊泡形成和左右模式形成中的调节功能提供了第一个证据。