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初级 microRNA 前体转录本定位于成年小鼠大脑前脑的突触后密度处。

Primary microRNA precursor transcripts are localized at post-synaptic densities in adult mouse forebrain.

机构信息

Department of Psychiatry and Psychiatric Institute, University of Illinois at Chicago, Chicago, IL 60612, USA.

出版信息

J Neurochem. 2012 Nov;123(4):459-66. doi: 10.1111/j.1471-4159.2012.07921.x. Epub 2012 Sep 28.

Abstract

In a previous study, we reported that microRNA (miRNA) precursors are expressed in synaptic fractions within adult mouse forebrain, where they are enriched at post-synaptic densities (PSDs). However, because that study employed qRT-PCR primers that recognize the hairpin region, it was not able to distinguish between primary microRNA gene transcripts (pri-miRs) and small hairpin precursors (pre-miRs). Here, using primer sets that selectively measure regions upstream, downstream and flanking the hairpin, we demonstrate that pri-miRs are present in synaptic fractions (enriched several-fold relative to total tissue homogenate) and are especially enriched in isolated PSDs. Drosha and DGCR8 proteins are also expressed in synaptic fractions and PSDs, and are tightly associated with pri-miRs as assessed by coimmunoprecipitation under stringent conditions. Pri-miRs, drosha, and DGCR8 are highly enriched in fractions that contain mRNA transport particles, and cytosolic drosha is associated with kinesin heavy chain; these findings suggest that pri-miRs are transported to synaptic regions in a manner similar to mRNAs. This study supports the notion that miRNA biogenesis occurs locally near synapses in a regulated fashion.

摘要

在之前的研究中,我们报道了 microRNA (miRNA) 前体在成年小鼠前脑中的突触部分表达,它们在突触后密度(PSD)处富集。然而,由于该研究采用的 qRT-PCR 引物识别发夹区,因此无法区分初级 microRNA 基因转录本(pri-miRs)和小发夹前体(pre-miRs)。在这里,我们使用选择性测量发夹上下游和侧翼区域的引物集,证明 pri-miRs 存在于突触部分(相对于组织总匀浆富集几倍),并且在分离的 PSD 中特别富集。Drosha 和 DGCR8 蛋白也在突触部分和 PSD 中表达,并通过严格条件下的共免疫沉淀评估与 pri-miRs 紧密相关。pri-miRs、Drosha 和 DGCR8 在含有 mRNA 转运颗粒的部分高度富集,细胞质中的 Drosha 与驱动蛋白重链相关;这些发现表明 pri-miRs 以类似于 mRNAs 的方式被运输到突触区域。这项研究支持了 miRNA 生物发生以受调控的方式在突触附近局部发生的观点。

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