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人α1-抗胰蛋白酶基因在大鼠肝癌×人成纤维细胞杂交细胞系中的激活与去甲基化相关。

Activation of human alpha 1-antitrypsin genes in rat hepatoma x human fibroblast hybrid cell lines is correlated with demethylation.

作者信息

Barton D E, Francke U

机构信息

Department of Human Genetics, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Somat Cell Mol Genet. 1987 Nov;13(6):635-44. doi: 10.1007/BF01534484.

Abstract

Alpha-1-antitrypsin (AAT) is the major protease inhibitor in human serum and is primarily expressed in the liver. We have studied AAT expression in fusion hybrids between a rat hepatoma line and either human fetal liver fibroblasts (series XXII) or human skin fibroblasts (series XIX). While the human AAT gene was always activated in series XXII hybrids when it was present, it was only rarely activated in series XIX hybrids. RFLP analysis revealed that both parental AAT alleles in series XIX hybrids were capable of being activated. Molecular analysis of the AAT gene in expressing and nonexpressing hybrids revealed that active AAT genes were hypomethylated, while inactive AAT genes were highly methylated. However, differences in methylation patterns were confined to the 5' end of the gene, on both sides of the first exon. DNaseI sensitivity revealed no hypersensitive sites close to active or inactive AAT genes.

摘要

α-1-抗胰蛋白酶(AAT)是人类血清中的主要蛋白酶抑制剂,主要在肝脏中表达。我们研究了大鼠肝癌细胞系与人类胎儿肝成纤维细胞(XXII系列)或人类皮肤成纤维细胞(XIX系列)之间融合杂种中的AAT表达。虽然人类AAT基因在XXII系列杂种中存在时总是被激活,但在XIX系列杂种中很少被激活。限制性片段长度多态性(RFLP)分析表明,XIX系列杂种中的两个亲本AAT等位基因都能够被激活。对表达和不表达杂种中AAT基因的分子分析表明,活跃的AAT基因是低甲基化的,而不活跃的AAT基因是高度甲基化的。然而,甲基化模式的差异仅限于基因的5'端,在第一个外显子的两侧。脱氧核糖核酸酶I(DNaseI)敏感性分析显示,在活跃或不活跃的AAT基因附近没有超敏感位点。

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