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本文引用的文献

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Tumor necrosis factor-alpha allelic frequency and chromosome 6 allelic imbalance in patients with colorectal cancer.结直肠癌患者中肿瘤坏死因子-α等位基因频率及6号染色体等位基因失衡
Cancer Res. 1996 Jan 1;56(1):145-9.
2
Dense Alu clustering and a potential new member of the NF kappa B family within a 90 kilobase HLA class III segment.在一个90千碱基的HLA III类区域内存在密集的Alu簇以及NF-κB家族的一个潜在新成员。
Nat Genet. 1993 Feb;3(2):137-45. doi: 10.1038/ng0293-137.
3
Highly informative typing of the human TNF locus using six adjacent polymorphic markers.利用六个相邻的多态性标记对人类肿瘤坏死因子基因座进行高信息量分型。
Genomics. 1993 Apr;16(1):180-6. doi: 10.1006/geno.1993.1156.
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Polymorphism of the tumor necrosis factor beta gene in systemic lupus erythematosus: TNFB-MHC haplotypes.
Immunogenetics. 1993;37(6):449-54. doi: 10.1007/BF00222469.
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An allelic polymorphism within the human tumor necrosis factor alpha promoter region is strongly associated with HLA A1, B8, and DR3 alleles.人类肿瘤坏死因子α启动子区域内的一个等位基因多态性与HLA A1、B8和DR3等位基因密切相关。
J Exp Med. 1993 Feb 1;177(2):557-60. doi: 10.1084/jem.177.2.557.
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Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLA.多发性硬化症中的肿瘤坏死因子多态性:独立于 HLA 无额外关联。
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7
Tumor necrosis factor microsatellites in four European populations.四个欧洲人群中的肿瘤坏死因子微卫星
Hum Immunol. 1993 Nov;38(3):213-6. doi: 10.1016/0198-8859(93)90543-a.
8
Association of tumor necrosis factor (TNF) and class II major histocompatibility complex alleles with the secretion of TNF-alpha and TNF-beta by human mononuclear cells: a possible link to insulin-dependent diabetes mellitus.肿瘤坏死因子(TNF)及Ⅱ类主要组织相容性复合体等位基因与人类单核细胞分泌肿瘤坏死因子-α和肿瘤坏死因子-β的关系:与胰岛素依赖型糖尿病的可能联系。
Eur J Immunol. 1993 Jan;23(1):224-31. doi: 10.1002/eji.1830230135.
9
Lymphotoxin beta, a novel member of the TNF family that forms a heteromeric complex with lymphotoxin on the cell surface.淋巴毒素β,肿瘤坏死因子家族的一个新成员,它在细胞表面与淋巴毒素形成异源复合物。
Cell. 1993 Mar 26;72(6):847-56. doi: 10.1016/0092-8674(93)90574-a.
10
Large transcripts and sequence from a polymorphic 170 kb MHC region implicated in susceptibility to autoimmune disease.来自一个与自身免疫性疾病易感性相关的170 kb多态性MHC区域的大型转录本和序列。
Immunogenetics. 1994;39(1):15-20. doi: 10.1007/BF00171792.

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.

DOI:10.1128/cdli.4.1.79-84.1997
PMID:9008286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC170480/
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。