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首次发现血清素受体3E型基因的微小RNA - 510靶位点功能性变异与腹泻型肠易激综合征之间存在关联的证据。

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.

作者信息

Kapeller Johannes, Houghton Lesley A, Mönnikes Hubert, Walstab Jutta, Möller Dorothee, Bönisch Heinz, Burwinkel Barbara, Autschbach Frank, Funke Benjamin, Lasitschka Felix, Gassler Nikolaus, Fischer Christine, Whorwell Peter J, Atkinson Wendy, Fell Catherine, Büchner Karl J, Schmidtmann Marco, van der Voort Ivo, Wisser Anna-Sophia, Berg Thomas, Rappold Gudrun, Niesler Beate

机构信息

Department of Human Molecular Genetics, University of Heidelberg, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.

出版信息

Hum Mol Genet. 2008 Oct 1;17(19):2967-77. doi: 10.1093/hmg/ddn195. Epub 2008 Jul 9.

Abstract

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.

摘要

腹泻型肠易激综合征(IBS-D)是一种与血清素能系统功能障碍相关的复杂疾病。由于顺式调控变异可能在复杂疾病的病因中起作用,我们研究了血清素受体3亚基基因HTR3A和HTR3E的非翻译区(UTR)。在来自英国的200例IBS患者和100例健康对照的试点样本中进行了突变分析。新发现的HTR3E 3'-UTR变异c.*76G>A(rs62625044)与女性IBS-D相关(P = 0.033,OR = 8.53)。在一项复制研究中证实了这种关联,该研究包括来自德国的119例IBS-D患者和195例对照(P = 0.0046,OR = 4.92)。汇总分析结果显示c.*76G>A与女性IBS-D高度显著相关(P = 0.0002,OR = 5.39)。在报告基因检测中,c.*76G>A影响miR-510与HTR3E 3'-UTR的结合,并导致荧光素酶表达升高。原位杂交和逆转录-聚合酶链反应显示,HTR3E和miR-510在肠道上皮细胞中共定位。这是第一个表明血清素受体基因存在与微小RNA相关的表达调控的例子,其中顺式调控变异影响这种调控,并且似乎与女性IBS-D相关。

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