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肿瘤坏死因子/淋巴毒素基因座中的新型复合四核苷酸、二核苷酸微卫星多态性

Novel compound tetra-, dinucleotide microsatellite polymorphism in the tumor necrosis factor/lymphotoxin locus.

作者信息

Greenberg S J, Fujihara K, Selkirk S M, Yu F, Du T L, Glenister N, Hohmann P, Rickert M H, Spence P O, Miller C E, Jacobs L D

机构信息

Laboratory of Neuroimmunology and Neurovirology, Department of Neurology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.

出版信息

Clin Diagn Lab Immunol. 1997 Jan;4(1):79-84. doi: 10.1128/cdli.4.1.79-84.1997.

Abstract

A polymorphic (TGCG)n, tetranucleotide repeat was discovered juxtaposed to the (GT)n dinucleotide repeat that comprises the tumor necrosis factor a microsatellite (TNF) located telomeric to the tumor necrosis factor/lymphotoxin gene cluster. The degree of complexity of this compound tetra-,dinucleotide microsatellite consists of 16 potential alleles of combined length ranging from 24 to 54 bp. The pattern of frequencies of individual alleles belonging to the compound TNFa microsatellite was established from 52 healthy volunteers and was found to be highly heterogeneous. The data diverges significantly from previously published statistics that recognized only a simple variable dinucleotide tandem repeat. The newly recognized compound tetra-, dinucleotide TNFa microsatellite polymorphism establishes a more accurate genetic basis to explore potential linkage with disease susceptibility genes located within this region of the class III major histocompatibility complex. In addition, variable tumor necrosis factor and lymphotoxin production may reflect the more complex polymorphic nature of this microsatellite region. Finally, compound microsatellites probably exist elsewhere, throughout the human genome. Recognition of their presence may have a considerable impact on the validity of past and future microsatellite-based genetic analyses.

摘要

发现一个多态性的(TGCG)n四核苷酸重复序列紧邻(GT)n二核苷酸重复序列,该二核苷酸重复序列构成了位于肿瘤坏死因子/淋巴毒素基因簇端粒侧的肿瘤坏死因子α微卫星(TNF)。这种复合的四核苷酸、二核苷酸微卫星的复杂程度由16个潜在等位基因组成,其组合长度范围为24至54 bp。从52名健康志愿者中确定了属于复合肿瘤坏死因子α微卫星的各个等位基因的频率模式,发现其具有高度的异质性。这些数据与之前仅认可简单可变二核苷酸串联重复的统计数据有显著差异。新发现的复合四核苷酸、二核苷酸肿瘤坏死因子α微卫星多态性为探索与位于III类主要组织相容性复合体该区域内的疾病易感基因的潜在连锁关系建立了更准确的遗传基础。此外,肿瘤坏死因子和淋巴毒素产生的变化可能反映了该微卫星区域更复杂的多态性本质。最后,复合微卫星可能在整个人类基因组的其他地方也存在。认识到它们的存在可能会对过去和未来基于微卫星的基因分析的有效性产生相当大的影响。

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