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大脑中体细胞DNA变异的研究:5-羟色胺2A受体基因的调查

Search for somatic DNA variation in the brain: investigation of the serotonin 2A receptor gene.

作者信息

Kaminsky Zachary A, Popendikyte Violeta, Assadzadeh Abbas, Petronis Arturas

机构信息

The Krembil Family Epigenetics Laboratory, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario, M5T 1R8, Canada.

出版信息

Mamm Genome. 2005 Aug;16(8):587-93. doi: 10.1007/s00335-005-0040-0. Epub 2005 Sep 14.

DOI:10.1007/s00335-005-0040-0
PMID:16180140
Abstract

Somatic DNA variation represents one of the most interesting but also one of the least investigated genetic phenomena. In addition to the classical case of DNA hypermutability at the V(D)J region, there is an increasing body of experimental evidence suggesting that genes other than immunoglobulin in tissues other than lymphocytes also exhibit nonuniformity of DNA sequence, which opens new opportunities for explaining various features of multicellular organisms. Identification of somatic DNA mutability, however, is not a trivial task and numerous confounding factors have to be taken into account. In this work we investigated putative DNA variation in the serotonin 2A receptor gene (HTR2A). A series of real-time PCR-based experiments was performed on DNA samples (n = 8) from human brain and peripheral leukocytes. Amplification of the target DNA sequences was carefully matched to that of the control plasmid containing the insert of HTR2A. Sequencing of nearly 500 clones containing a total of 150,000 nucleotides did not show any evidence for somatic DNA variation in the brain and peripheral leukocytes. It is argued in this article that although intraindividual DNA mutability may be a more common phenomenon than is generally accepted, some of the earlier claims of genetic nonidentity on the brain cells may be premature.

摘要

体细胞DNA变异是最有趣但也是研究最少的遗传现象之一。除了V(D)J区域DNA高突变的经典案例外,越来越多的实验证据表明,淋巴细胞以外的组织中除免疫球蛋白外的其他基因也表现出DNA序列的不均匀性,这为解释多细胞生物的各种特征提供了新的机会。然而,鉴定体细胞DNA突变并非易事,必须考虑众多混杂因素。在这项工作中,我们研究了血清素2A受体基因(HTR2A)中假定的DNA变异。对来自人脑和外周血白细胞的DNA样本(n = 8)进行了一系列基于实时PCR的实验。目标DNA序列的扩增与含有HTR2A插入片段的对照质粒的扩增进行了仔细匹配。对近500个克隆(共150,000个核苷酸)进行测序,未发现脑和外周血白细胞中存在体细胞DNA变异的任何证据。本文认为,尽管个体内DNA突变可能是一种比普遍接受的更为常见的现象,但一些早期关于脑细胞遗传非同一性的说法可能为时过早。

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Chromosome segregation defects contribute to aneuploidy in normal neural progenitor cells.染色体分离缺陷会导致正常神经祖细胞出现非整倍体。
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Somatic mutations of synaptic cadherin (CNR family) transcripts in the nervous system.神经系统中突触钙黏蛋白(CNR家族)转录本的体细胞突变。
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