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人类胸腺嘧啶-DNA糖基化酶定位于12号染色体q22-q24.1区域:这是胃癌中杂合性高缺失的一个区域。

Human thymine-DNA glycosylase maps at chromosome 12q22-q24.1: a region of high loss of heterozygosity in gastric cancer.

作者信息

Schmutte C, Baffa R, Veronese L M, Murakumo Y, Fishel R

机构信息

Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Cancer Res. 1997 Jul 15;57(14):3010-5.

PMID:9230216
Abstract

Spontaneous hydrolytic deamination of 5-methylcytosine leads to T:G mismatches in double-stranded DNA and comprises a major threat for the integrity of both the DNA primary sequence as well as the epigenetic information stored in the DNA methylation pattern. Failure of the cellular DNA repair machinery to recognize and repair such mismatched nucleotides can lead to a mutator phenotype and subsequent carcinogenesis. A thymine-DNA glycosylase (TDG) has been described that initiates T:G mismatch repair by specifically excising the mismatched T. We have studied the TDG genomic locus and the expression of this enzyme to evaluate its role in cancer development. TDG is highly expressed in thymus and is expressed at lower levels in all human tissues analyzed. The TDG gene has 10 exons covering a region of >25 kb and is located on chromosome 12q22-q24.1. Because gastric tumors have been shown to contain a high percentage of C-->T mutations at CpG sites, we used a microsatellite found in intron 8 of the TDG locus to screen gastric tumor samples for loss of heterozygosity. Although our analysis showed loss of heterozygosity in 10 of 24 samples (42%), none of those tumor samples revealed a mutation in the coding sequence of the remaining TDG allele as analyzed by single-strand conformational polymorphism. Expression of the TDG was not determined because of the limited availability of RNA in these primary tumor samples. At present, we have found no evidence that TDG is central to the development of gastric cancer, limiting the importance of TDG in T:G mismatch repair and subsequent carcinogenesis.

摘要

5-甲基胞嘧啶的自发水解脱氨作用会导致双链DNA中出现T:G错配,这对DNA一级序列的完整性以及存储在DNA甲基化模式中的表观遗传信息都构成了重大威胁。细胞DNA修复机制若无法识别和修复此类错配核苷酸,可能会导致突变体表型及随后的癌变。已发现一种胸腺嘧啶-DNA糖基化酶(TDG),它通过特异性切除错配的胸腺嘧啶来启动T:G错配修复。我们研究了TDG基因座及该酶的表达,以评估其在癌症发生中的作用。TDG在胸腺中高度表达,在所有分析的人体组织中表达水平较低。TDG基因有10个外显子,覆盖区域大于25 kb,位于12号染色体q22-q24.1区域。由于已表明胃肿瘤在CpG位点含有高比例的C→T突变,我们利用在TDG基因座内含子8中发现的一个微卫星来筛选胃肿瘤样本中的杂合性缺失。尽管我们的分析显示24个样本中有10个(42%)存在杂合性缺失,但通过单链构象多态性分析,这些肿瘤样本中没有一个在剩余TDG等位基因的编码序列中发现突变。由于这些原发性肿瘤样本中RNA的可获得量有限,未测定TDG的表达。目前,我们没有发现证据表明TDG在胃癌发生中起核心作用,这限制了TDG在T:G错配修复及随后癌变中的重要性。

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