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实验鉴定人类 FMR1 基因 3'UTR 上的 microRNA 靶标。

Experimental identification of microRNA targets on the 3' untranslated region of human FMR1 gene.

机构信息

Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and The Ministry of Education of China, Institute of Neuroscience and The Second Affiliated Hospital of Guangzhou Medical University, 250 Chang-gang-dong Road, Guangzhou 510260, China.

出版信息

J Neurosci Methods. 2010 Jun 30;190(1):34-8. doi: 10.1016/j.jneumeth.2010.04.022. Epub 2010 May 9.

Abstract

FMR1 gene plays an important role in the development of central nervous system. Down-regulation of the FMR1 expression leads to fragile X syndrome. MicroRNAs (miRNAs) can repress gene expression by base pairing with their mRNA targets. By computer programs analysis, five miRNAs: miR-19a, miR-19b, miR-142, miR-302b* and miR-323-3p potentially target to different sites on the FMR1 3' untranslated region (3' UTR), except that miR-19a and miR-19b share the same targeting site. To test whether these miRNAs repress reporter gene expression by interacting with the miRNA targets on the FMR1 3' UTR, we developed two chimeric constructs: one construct expressing a firefly luciferase with the FMR1 3' UTR or its miRNA target mutations and the other construct expressing a pre-miRNA fusing with GFP. Luciferase assay co-transfecting with the two constructs showed that the miRNAs, miR-19b, miR-302b* and miR-323-3p could repress gene expression in HEK-293 cells, suggesting a role of these miRNAs in the regulation of the FMR1 expression. The constructs used in this study can be widely used to identify the miRNA targets in any interested genes, which will greatly promote the current progress in understanding the biological function of miRNAs.

摘要

脆性 X 智力低下 1 基因(FMR1)在中枢神经系统的发育中起着重要作用。FMR1 表达的下调导致脆性 X 综合征。微小 RNA(miRNA)可以通过与它们的 mRNA 靶标碱基配对来抑制基因表达。通过计算机程序分析,有 5 种 miRNA(miR-19a、miR-19b、miR-142、miR-302b和 miR-323-3p)可能靶向 FMR1 3'非翻译区(3'UTR)上的不同位点,除了 miR-19a 和 miR-19b 共享相同的靶位点。为了测试这些 miRNA 是否通过与 FMR1 3'UTR 上的 miRNA 靶标相互作用来抑制报告基因的表达,我们构建了两个嵌合构建体:一个表达萤火虫荧光素酶与 FMR1 3'UTR 或其 miRNA 靶标突变,另一个表达与 GFP 融合的 pre-miRNA。共转染这两种构建体的荧光素酶测定表明,miR-19b、miR-302b和 miR-323-3p 可以在 HEK-293 细胞中抑制基因表达,表明这些 miRNA 在 FMR1 表达调控中发挥作用。本研究中使用的构建体可广泛用于鉴定任何感兴趣基因中的 miRNA 靶标,这将极大地促进对 miRNA 生物学功能的理解。

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