正常和衰老人类成纤维细胞中与hnRNP A1结合的RNA种类的鉴定

Heriberto Moran, Shanaz A. Ghandhi, N. Shimada, K. Hubbard
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引用次数: 0

摘要

hnRNP A1是hnRNPs(异质核核糖核蛋白)蛋白家族的一员,在调节负责细胞增殖、DNA修复、细胞凋亡和端粒生物发生的基因中起核心作用。先前的研究表明,hnRNPA1在衰老的人类二倍体成纤维细胞中降低了蛋白水平并增加了细胞质积累。蛋白质表达减少和细胞定位改变的结果可能解释了在衰老过程中观察到的基因表达的改变。关于hnRNP A1的基因靶点及其体内功能的信息有限。在这些研究中,我们使用hnRNP A1作为靶蛋白进行RNA共免疫沉淀实验,以鉴定核糖核蛋白(RNP)复合物中潜在的mRNA种类。利用这种方法,我们在年轻和衰老的人类二倍体成纤维细胞中发现了人类双分钟2 (HDM2) mRNA作为hnRNP A1的结合靶点。还观察到hnRNP A1表达的改变可调节年轻IMR-90细胞中HDM2 mRNA的水平。我们还发现,HDM2 mRNA水平随着hnRNP A1的下调而升高,而随着hnRNP A1的过表达而降低。虽然我们没有观察到HDM2蛋白水平的显著下降,但在hnRNP A1过表达的同时,p53蛋白水平也随之升高。我们的研究还表明,hnRNP A1在其3 ' UTR(基因的非翻译区)对应的区域直接与HDM2 mRNA相互作用。本研究结果表明,hnRNP A1在参与HDM2基因表达调控中具有新的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of RNA Species That Bind to the hnRNP A1 in Normal and Senescent Human Fibroblasts
hnRNP A1 is a member of the hnRNPs (heterogeneous nuclear ribonucleoproteins) family of proteins that play a central role in regulating genes responsible for cell proliferation, DNA repair, apoptosis, and telomere biogenesis. Previous studies have shown that hnRNPA1 had reduced protein levels and increased cytoplasmic accumulation in senescent human diploid fibroblasts. The consequence of reduced protein expression and altered cellular localization may account for the alterations in gene expression observed during senescence. There is limited information for gene targets of hnRNP A1 as well as its in vivo function. In these studies, we performed RNA co-immunoprecipitation experiments using hnRNP A1 as the target protein to identify potential mRNA species in ribonucleoprotein (RNP) complexes. Using this approach, we identified the human double minute 2 (HDM2) mRNA as a binding target for hnRNP A1 in young and senescent human diploid fibroblasts cells. It was also observed that alterations of hnRNP A1 expression modulate HDM2 mRNA levels in young IMR-90 cells. We also demonstrated that the levels of HDM2 mRNA increased with the downregulation of hnRNP A1 and decrease with the overexpression of hnRNP A1. Although we did not observe a significant decrease in HDM2 protein level, a concomitant increase in p53 protein level was detected with the overexpression of hnRNP A1. Our studies also show that hnRNP A1 directly interacts with HDM2 mRNA at a region corresponding to its 3′ UTR (untranslated region of a gene). The results from this study demonstrate that hnRNP A1 has a novel role in participating in the regulation of HDM2 gene expression.
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