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核激素介导的染色质溶解度变化。

Nuclear-hormone mediated changes in chromatin solubility.

作者信息

Re R N, LaBiche R A, Bryan S E

出版信息

Biochem Biophys Res Commun. 1983 Jan 14;110(1):61-8. doi: 10.1016/0006-291x(83)91260-3.

Abstract

Rat liver nuclei were incubated with either thyroid hormone or angiotensin (AII) at varying concentrations or with buffer (control) prior to digestion with micrococcal nuclease. Concentrations of hormones greater than 10(-10)M were effective in increasing the solubilization of chromatin with physiological levels (10(-9)M) of AII showing an approximate 2.4 fold increase over control. Nuclei were also isolated from animals treated in-vivo with either AII or buffer (control) and chromatin solubility was increased in the AII treated nuclei even prior to the addition of exogenous nuclease, presumably from the action of endogenous nucleases. The data suggest that hormone-induced increases in solubility are a reflection of structural changes in chromatin which enhance the accessibility of DNA to endonuclease attack.

摘要

在用微球菌核酸酶消化之前,将大鼠肝细胞核与不同浓度的甲状腺激素或血管紧张素(AII)或缓冲液(对照)一起孵育。浓度大于10(-10)M的激素可有效增加染色质的溶解,生理水平(10(-9)M)的AII使溶解比对照增加约2.4倍。还从体内用AII或缓冲液(对照)处理的动物中分离细胞核,即使在添加外源核酸酶之前,AII处理的细胞核中的染色质溶解度也增加,这可能是内源性核酸酶作用的结果。数据表明,激素诱导的溶解度增加反映了染色质结构的变化,这种变化增强了DNA对内切核酸酶攻击的可及性。

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