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[氢化可的松对大鼠肝脏DNA甲基化及分子群体的影响]

[Effect of hydrocortisone on methylation and molecular population of DNA in rat liver].

作者信息

Romanov G A, Kir'ianov G I, Dvorkin V M, Vaniushin B F

出版信息

Biokhimiia. 1976 Jul;41(6):1038-43.

PMID:1027486
Abstract

The content of 5-methyl cytosine in rat liver DNA increases 1,7-fold 8 hours after intraperitoneal injection of hydrocortisone (5 mg per 100 g animal weight). The content of GC, physicochemical parameters (Tm, delta T, etc.) and DNA renaturation pattern did not show any changes. No changes were observed in the pattern of H3-thymidine incorporation into rat liver DNA: after hydrocortisone injection the radioactivity was found to be equally distributed in all isolated sequences of DNA, differing in the degree of reiteration (specific radioactivities of these DNA, fractions are very similar). Thus, the molecular population of DNA in liver cells remains unchanged, which suggests that the hormone-induced increase in the 5-methyl cytosine content is due to a change in the DNA methylation level. The methyation level of unique sequences (COt greater than 600), i. e. that of structural genes, does not undergo any essential changes. The reversible methylation of DNA regulated by hormones seems to be one of the mechanisms controlling gene activity.

摘要

腹腔注射氢化可的松(每100克动物体重5毫克)8小时后,大鼠肝脏DNA中5-甲基胞嘧啶的含量增加了1.7倍。GC含量、物理化学参数(熔点、熔解温度范围等)以及DNA复性模式均未显示出任何变化。在H3-胸腺嘧啶掺入大鼠肝脏DNA的模式中未观察到变化:注射氢化可的松后,放射性在所有分离出的DNA序列中均匀分布,这些序列的重复程度不同(这些DNA片段的比放射性非常相似)。因此,肝细胞中DNA的分子群体保持不变,这表明激素诱导的5-甲基胞嘧啶含量增加是由于DNA甲基化水平的改变。单一序列(Cot大于600),即结构基因的甲基化水平没有发生任何实质性变化。激素调节的DNA可逆甲基化似乎是控制基因活性的机制之一。

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