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首页> 外文期刊>Human Molecular Genetics >First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.
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First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.

机译:血清素受体3E型基因的microRNA-510靶位点功能性变异与腹泻型肠易激综合征相关的第一个证据。

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摘要

Diarrhea predominant irritable bowel syndrome (IBS-D) is a complex disorder related to dysfunctions in the serotonergic system. As cis-regulatory variants can play a role in the etiology of complex conditions, we investigated the untranslated regions (UTRs) of the serotonin receptor type 3 subunit genes HTR3A and HTR3E. Mutation analysis was carried out in a pilot sample of 200 IBS patients and 100 healthy controls from the UK. The novel HTR3E 3'-UTR variant c.*76G>A (rs62625044) was associated with female IBS-D (P = 0.033, OR = 8.53). This association was confirmed in a replication study, including 119 IBS-D patients and 195 controls from Germany (P = 0.0046, OR = 4.92). Pooled analysis resulted in a highly significant association of c.*76G>A with female IBS-D (P = 0.0002, OR = 5.39). In a reporter assay, c.*76G>A affected binding of miR-510 to the HTR3E 3'-UTR and caused elevated luciferase expression. HTR3E and miR-510 co-localize in enterocytes of the gut epithelium as shown by in situ hybridization and RT-PCR. This is the first example indicating micro RNA-related expression regulation of a serotonin receptor gene with a cis-regulatory variant affecting this regulation and appearing to be associated with female IBS-D.
机译:腹泻型肠易激综合症(IBS-D)是与血清素能系统功能障碍有关的复杂疾病。由于顺式调节变体可以在复杂条件的病因中发挥作用,因此我们研究了血清素受体3型亚基基因HTR3A和HTR3E的非翻译区(UTR)。在来自英国的200名IBS患者和100名健康对照的试验样本中进行了突变分析。新型HTR3E 3'-UTR变体c。* 76G> A(rs62625044)与雌性IBS-D(P = 0.033,OR = 8.53)相关。在一项复制研究中证实了这一关联,包括来自德国的119名IBS-D患者和195名对照(P = 0.0046,OR = 4.92)。合并分析导致c。* 76G> A与雌性IBS-D高度相关(P = 0.0002,OR = 5.39)。在报告基因分析中,c。* 76G> A影响了miR-510与HTR3E 3'-UTR的结合并导致荧光素酶表达升高。 HTR3E和miR-510共定位在肠道上皮的肠上皮细胞中,如原位杂交和RT-PCR所示。这是第一个表明5-羟色胺受体基因的微RNA相关表达调控的顺式调控变体,影响该调控,并且似乎与雌性IBS-D有关。

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