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中国仓鼠X人杂交细胞中X连锁基因的高频激活

High-frequency reactivation of X-linked genes in Chinese hamster X human hybrid cells.

作者信息

Ellis N, Keitges E, Gartler S M, Rocchi M

出版信息

Somat Cell Mol Genet. 1987 May;13(3):191-204. doi: 10.1007/BF01535202.

Abstract

Three genes on the human inactive X chromosome retained in the Chinese hamster X human hybrid cell line X8/6T2 have been reactivated using the demethylating agent, 5-azacytidine (5-aza-CR). Pulse-labeling and histochemical methods permitted detection and measurement of reactivation rates of the hypoxanthine phosphoribosyltransferase (Hpt) and glucose-6-phosphate dehydrogenase (G6pd) genes within 48 h of treatment. About 50% of the cells became active for these genes, which represents a reactivation rate some 30-fold greater than previously reported in similar systems. The phosphoglycerate kinase (Pgk) gene was not reactivated as frequently as the Hpt or G6pd genes. Segregation analysis of progeny of treated cells showed that enzyme-positive and enzyme-negative cells were produced in proportions supporting the notion that 5-aza-CR causes demethylation by replicative loss and that demethylation leads to reactivation.

摘要

利用去甲基化剂5-氮杂胞苷(5-aza-CR),中国仓鼠X人杂交细胞系X8/6T2中保留的人类失活X染色体上的三个基因已被重新激活。脉冲标记和组织化学方法能够在处理后48小时内检测并测量次黄嘌呤磷酸核糖基转移酶(Hpt)和葡萄糖-6-磷酸脱氢酶(G6pd)基因的重新激活率。约50%的细胞对这些基因变得活跃,这代表的重新激活率比之前在类似系统中报道的高出约30倍。磷酸甘油酸激酶(Pgk)基因的重新激活频率不如Hpt或G6pd基因高。对处理后细胞后代的分离分析表明,产生的酶阳性和酶阴性细胞比例支持这样一种观点,即5-aza-CR通过复制性丢失导致去甲基化,而去甲基化导致重新激活。

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