Zabinsky Rebecca A, Weum Brett M, Cui Mingxue, Han Min
Howard Hughes Medical Institute, University of Colorado at Boulder, Boulder, Colorado 80309.
Howard Hughes Medical Institute, University of Colorado at Boulder, Boulder, Colorado 80309
G3 (Bethesda). 2017 Aug 7;7(8):2511-2518. doi: 10.1534/g3.117.043414.
Extensive studies have suggested that most miRNA functions are executed through complex miRNA-target interaction networks, and such networks function semiredundantly with other regulatory systems to shape gene expression dynamics for proper physiological functions. We found that knocking down , which encodes a conserved RNA-binding protein associated with diverse functions, causes severe larval arrest at the early L1 stage in animals with compromised miRISC functions (an mutant). Through an enhancer screen, we identified five specific miRNAs, and miRNA families, that act semiredundantly with VGLN-1 to regulate larval development. By RIP-Seq analysis, we identified mRNAs that are directly bound by VGLN-1, and highly enriched for miRNA binding sites, leading to a hypothesis that VGLN-1 may share common targets with miRNAs to regulate gene expression dynamics for development.
广泛的研究表明,大多数miRNA的功能是通过复杂的miRNA-靶标相互作用网络来执行的,并且这些网络与其他调节系统半冗余发挥作用,以塑造基因表达动态从而实现适当的生理功能。我们发现,敲低编码一种与多种功能相关的保守RNA结合蛋白的 ,会导致miRISC功能受损的动物(一种 突变体)在L1早期阶段出现严重的幼虫发育停滞。通过增强子筛选,我们鉴定出了五个特定的miRNA以及miRNA家族,它们与VGLN-1半冗余发挥作用来调节幼虫发育。通过RIP-Seq分析,我们鉴定出了与VGLN-1直接结合的mRNA,并且这些mRNA高度富集miRNA结合位点,从而得出一个假设,即VGLN-1可能与miRNA共享共同的靶标来调节发育过程中的基因表达动态。