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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >The DEAH-box helicase DHX36 mediates dendritic localization of the neuronal precursor-microRNA-134
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The DEAH-box helicase DHX36 mediates dendritic localization of the neuronal precursor-microRNA-134

机译:DEAH盒解旋酶DHX36介导神经元前体microRNA-134的树突状定位。

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摘要

SpecificmicroRNAs (miRNAs), includingmiR-134, localize to neuronal dendrites, where they control synaptic protein synthesis and plasticity. However, the mechanism of miRNA transport is unknown.We found that the neuronal precursor-miRNA-134 (pre-miR-134) accumulates in dendrites of hippocampal neurons and at synapses in vivo. Dendritic localization of pre-miR-134 is mediated by the DEAH-box helicase DHX36, which directly associates with the pre-miR-134 terminal loop. DHX36 function is required for miR-134-dependent inhibition of target gene expression and the control of dendritic spine size. Dendritically localized pre-miR-134 could provide a local source of miR-134 that can be mobilized in an activitydependent manner during plasticity.
机译:特定的microRNA(miRNA),包括miR-134,位于神经元树突中,它们控制突触蛋白的合成和可塑性。然而,miRNA转运的机制尚不清楚。我们发现神经元前体miRNA-134(pre-miR-134)积累在海马神经元的树突中和体内的突触中。 pre-miR-134的树突状定位是由DEAH-box解旋酶DHX36介导的,该酶直接与pre-miR-134末端环缔合。 DHX36功能是miR-134依赖性抑制靶基因表达和控制树突棘大小所必需的。局部定位的pre-miR-134可提供miR-134的局部来源,可在活动过程中以活动依赖的方式进行动员。

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