Suppr超能文献

鉴定和功能特征的极长等位基因的血清素转运体相关多态区。

Identification and functional characterization of the extremely long allele of the serotonin transporter-linked polymorphic region.

机构信息

Department of Neuropsychiatry, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Department of Neuropsychiatry, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

出版信息

Transl Psychiatry. 2021 Feb 11;11(1):119. doi: 10.1038/s41398-021-01242-9.

Abstract

SLC6A4, which encodes the serotonin transporter, has a functional polymorphism called the serotonin transporter-linked polymorphic region (5-HTTLPR). The 5-HTTLPR consists of short (S) and long (L) alleles, each of which has 14 or 16 tandem repeats. In addition, the extralong (XL) and other rare alleles have been reported in 5-HTTLPR. Although they are more frequent in Asian and African than in other populations, the extent of variations and allele frequencies (AFs) were not addressed in a large population. Here, we report the AFs of the rare alleles in a large number of Japanese subjects (N = 2894) consisting of two cohorts. The first cohort (case-control study set, CCSS) consisted of 1366 subjects, including 485 controls and 881 patients with psychosis (bipolar disorder or schizophrenia). The second cohort (the Arao cohort study set, ACSS) consisted of 1528 elderly subjects. During genotyping, we identified 11 novel 5-HTTLPR alleles, including 3 XL alleles. One novel allele had the longest subunit ever reported, consisting of 28 tandem repeats. We named this XL An in vitro luciferase assay revealed that XL has no transcriptional activity. XL was found in two unrelated patients with bipolar disorder in the CCSS and one healthy subject in the ACSS who did not show depressive symptoms or a decline in cognitive function. Therefore, it is unlikely that XL is associated with psychiatric disorders, despite its apparent functional deficit. Our results suggest that unraveling the complex genetic variations of 5-HTTLPR will be important for further understanding its role in psychiatric disorders.

摘要

SLC6A4 基因编码 5-羟色胺转运体,其存在一个功能多态性,称为 5-羟色胺转运体基因连锁多态区(5-HTTLPR)。5-HTTLPR 由短(S)和长(L)等位基因组成,每个等位基因具有 14 或 16 个串联重复。此外,在 5-HTTLPR 中还报道了超长(XL)和其他罕见等位基因。尽管它们在亚洲和非洲人群中比其他人群更为常见,但在大规模人群中尚未涉及这些变异和等位基因频率(AF)的程度。在这里,我们报告了来自两个队列的大量日本受试者(N=2894)中罕见等位基因的 AF。第一个队列(病例对照研究集,CCSS)包括 1366 名受试者,包括 485 名对照和 881 名精神病患者(双相情感障碍或精神分裂症)。第二个队列(Arao 队列研究集,ACSS)由 1528 名老年受试者组成。在基因分型过程中,我们确定了 11 个新的 5-HTTLPR 等位基因,包括 3 个 XL 等位基因。一个新的等位基因具有报告的最长亚基,由 28 个串联重复组成。我们将其命名为 XLAn。体外荧光素酶测定表明 XL 没有转录活性。在 CCSS 中,两个无关的双相情感障碍患者和 ACSS 中一个没有抑郁症状或认知功能下降的健康受试者中发现了 XL。因此,尽管 XL 具有明显的功能缺陷,但它不太可能与精神疾病相关。我们的研究结果表明,阐明 5-HTTLPR 的复杂遗传变异对于进一步理解其在精神疾病中的作用非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7a4/7878853/972ad9bfa343/41398_2021_1242_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验