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5-HTTLPR 和 SNP 启动子多态性对 5-羟色胺转运体基因表达的作用:常见和罕见等位基因变异的遗传结构和体外功能研究的深入探讨。

Role of the 5-HTTLPR and SNP Promoter Polymorphisms on Serotonin Transporter Gene Expression: a Closer Look at Genetic Architecture and In Vitro Functional Studies of Common and Uncommon Allelic Variants.

机构信息

National Research Council (CNR), Institute of Translational Pharmacology (IFT), via Fosso del Cavaliere 100, 00133, Rome, Italy.

Geriatric Unit and Gerontology-Geriatrics Research Laboratory, Department of Medical Sciences, IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini 1, 71013, San Giovanni Rotondo, Foggia, Italy.

出版信息

Mol Neurobiol. 2016 Oct;53(8):5510-26. doi: 10.1007/s12035-015-9409-6. Epub 2015 Oct 13.

Abstract

The serotonin (5-hydroxytriptamine (5-HT)) transporter (5-HTT) gene-linked polymorphic region (5-HTTLPR) is a variable number tandem repeats (VNTR) located in the promoter region of the human 5-HTT-encoding gene SLC6A4. This length polymorphism gives rise to different promoter variants, variously influencing SLC6A4 expression. Over the years, an extensive literature has investigated the relationships between these promoter variants and SLC6A4 gene expression, since these variants have been variously associated to complex neuropsychiatric conditions and traits. In this review, we detail the genetic architecture of the 5-HTTLPR allelic variants reported so far, with a closer look at the two single nucleotide polymorphisms (SNPs) rs25531 and rs25532 that lies in the VNTR and thus increase genetic variability of the SLC6A4 promoter. We summarize the hypothesized molecular mechanisms underlying this variation. We also provide an update on common and uncommon 5-HTTLPR allelic variants reviewing the available data on functional in vitro analysis of their regulatory effect on SLC6A4 gene transcription. Controversial findings are highlighted and critically discussed. A deeper knowledge of the "5-HTTLPR universe" will be useful to better understand the molecular basis of serotonin homeostasis and the pathological basis underlying serotonin-related neuropsychiatric conditions and traits.

摘要

血清素(5-羟色胺(5-HT))转运体(5-HTT)基因连锁多态区(5-HTTLPR)是位于人类 5-HTT 编码基因 SLC6A4 启动子区域的可变数目串联重复(VNTR)。这种长度多态性产生不同的启动子变体,从而影响 SLC6A4 的表达。多年来,大量文献研究了这些启动子变体与 SLC6A4 基因表达之间的关系,因为这些变体与复杂的神经精神疾病和特征有多种关联。在这篇综述中,我们详细介绍了迄今为止报道的 5-HTTLPR 等位变体的遗传结构,并仔细研究了位于 VNTR 中的两个单核苷酸多态性(SNP)rs25531 和 rs25532,它们增加了 SLC6A4 启动子的遗传变异性。我们总结了这种变异的假设分子机制。我们还通过对其对 SLC6A4 基因转录的调节作用的体外功能分析的现有数据进行综述,提供了关于常见和罕见的 5-HTTLPR 等位变体的最新信息。突出显示并批判性地讨论了有争议的发现。深入了解“5-HTTLPR 宇宙”将有助于更好地理解血清素动态平衡的分子基础以及与血清素相关的神经精神疾病和特征的病理基础。

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