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Multiple cis-elements and trans-acting factors regulate dynamic spatio-temporal transcription of let-7 in C. elegans

机译:多种顺式元素和跨作用因子调节Let-7中的动态时空转录C. elegans

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摘要

The let-7 microRNA (miRNA) is highly conserved across animal phyla and generally regulates cellular differentiation and developmental timing pathways. In C. elegans, the mature let-7 miRNA starts to accumulate in the last stages of larval development where it directs cellular differentiation programs required for adult fates. Here we show that expression of the let-7 gene in C. elegans is under complex transcriptional control. The onset of let-7 transcription begins as early as the first larval stage in some tissues, and as late as the third larval stage in others, and is abrogated at the gravid adult stage. Transcription from two different start sites in the let-7 promoter oscillates during each larval stage. We show that transcription is regulated by two distinct cis-elements in the promoter of let-7, the previously described temporal regulatory element (TRE), and a novel element downstream of the TRE that we have named the let-7 transcription element (LTE). These elements play distinct and redundant roles in regulating let-7 expression in specific tissues. In the absence of the TRE and LTE, transcription of let-7 is undetectable and worms exhibit the lethal phenotype characteristic of let-7 null mutants. We also identify several genes that affect the transcription of let-7 generally and tissue-specifically. Overall, spatio-temporal regulation of let-7 transcription is orchestrated by multiple cis- and trans-acting factors to ensure appropriate expression of this essential miRNA during worm development.
机译:let-7 microRNA(miRNA)在整个动物门中高度保守,通常调节细胞分化和发育时间途径。在秀丽隐杆线虫中,成熟的let-7 miRNA在幼虫发育的最后阶段开始积累,在那里它指导成年命运所需的细胞分化程序。在这里,我们显示线虫中let-7基因的表达处于复杂的转录控制之下。 let-7转录的起始时间早于某些组织的幼虫期,而晚于其他组织的第三幼虫期,并在妊娠成年期被废止。在每个幼虫阶段,let-7启动子中两个不同起始位点的转录都会振荡。我们显示转录受let-7启动子中两个截然不同的顺式元件调控,先前描述的时间调控元件(TRE)和TRE下游的一种新型元件,我们将其命名为let-7转录元件(LTE )。这些元素在调节let-7在特定组织中的表达中起着独特而多余的作用。在没有TRE和LTE的情况下,let-7的转录是不可检测的,蠕虫表现出let-7 null突变体的致死表型特征。我们还鉴定了几个基因,这些基因一般和组织特异性地影响let-7的转录。总体而言,let-7转录的时空调控是由多个顺式和反式作用因子共同调控的,以确保在蠕虫发育过程中该基本miRNA的适当表达。

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