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大鼠精囊分泌蛋白IV基因的甲基化。在几个雄性附属性腺中发生广泛的去甲基化。

Methylation of the rat seminal vesicle secretory protein IV gene. Extensive demethylation occurs in several male sex accessory glands.

作者信息

Kandala J C, Kistler W S, Kistler M K

出版信息

J Biol Chem. 1985 Dec 15;260(29):15959-64.

PMID:2415526
Abstract

Seminal vesicle secretory protein IV (SVS IV) is perhaps the most abundant protein made by the epithelial cells of the rat seminal vesicle. In this report, we have asked whether the methylation of its gene correlates with its tissue-specific pattern of expression. Using methylation-sensitive restriction endonucleases HpaII and AvaI, we could examine seven potential methylation sites in or near the gene. All seven sites were largely unmethylated in the seminal vesicle, while in most nonexpressing organs, all sites were heavily modified. The correlation of demethylation with expression was broken by finding that both ventral prostate and coagulating gland (anterior prostate) DNA showed the same demethylation pattern seen for the seminal vesicle. SVS IV protein has not been reported in either of these two organs, and we could not detect mature SVS IV message in prostate RNA or SVS IV transcription by in vitro incubation of prostate nuclei. We conclude that demethylation of the SVS IV gene accompanies the differentiation of several androgen-dependent sex accessory glands but confirm that demethylation per se is not a sufficient signal to bring about gene transcription.

摘要

精囊分泌蛋白IV(SVS IV)可能是大鼠精囊上皮细胞产生的最为丰富的蛋白质。在本报告中,我们探讨了其基因的甲基化是否与其组织特异性表达模式相关。使用甲基化敏感限制性内切酶HpaII和AvaI,我们能够检测该基因内部或附近的七个潜在甲基化位点。在精囊中,所有七个位点大多未被甲基化,而在大多数不表达的器官中,所有位点都被高度修饰。通过发现腹侧前列腺和凝固腺(前前列腺)DNA呈现出与精囊相同的去甲基化模式,去甲基化与表达之间的相关性被打破。在这两个器官中均未报道过SVS IV蛋白,并且通过体外孵育前列腺细胞核,我们无法在前列腺RNA中检测到成熟的SVS IV信息或SVS IV转录。我们得出结论,SVS IV基因的去甲基化伴随着几种雄激素依赖性性附属腺的分化,但证实去甲基化本身并不是引发基因转录的充分信号。

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