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Demethylation of Histone H3K36 and H3K9 by Rph1: a Vestige of an H3K9 Methylation System in Saccharomyces cerevisiae?

机译:Rph1使组蛋白H3K36和H3K9脱甲基:酿酒酵母中H3K9甲基化系统的痕迹?

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Histone methylation is an important posttranslational modification that contributes to chromatin-based processes including transcriptional regulation, DNA repair, and epigenetic inheritance. In the budding yeast Saccharomyces cerevisiae, histone lysine methylation occurs on histone H3 lysines 4, 36, and 79, and its deposition is coupled mainly to transcription. Until recently, histone methylation was considered to be irreversible, but the identification of histone demethylase enzymes has revealed that this modification can be dynamically regulated. In budding yeast, there are five proteins that contain the JmjC domain, a signature motif found in a large family of histone demethylases spanning many organisms. One JmjC-domain-containing protein in budding yeast, Jhd1, has recently been identified as being a histone demethylase that targets H3K36 modified in the di- and monomethyl state. Here, we identify a second JmjC-domain-containing histone demethylase, Rph1, which can specifically demethylate H3K36 tri- and dimethyl modification states. Surprisingly, Rph1 can remove H3K9 methylation, a histone modification not found in budding yeast chromatin. The capacity of Rph1 to demethylate H3K9 provides the first indication that S. cerevisiae may have once encoded an H3K9 methylation system and suggests that Rph1 is a functional vestige of this modification system.
机译:组蛋白甲基化是重要的翻译后修饰,有助于基于染色质的过程,包括转录调控,DNA修复和表观遗传。在萌芽的酿酒酵母中,组蛋白赖氨酸甲基化发生在组蛋白H3赖氨酸4、36和79上,其沉积主要与转录相关。直到最近,组蛋白甲基化仍被认为是不可逆的,但是组蛋白脱甲基酶的鉴定表明该修饰可以动态调节。在出芽的酵母中,有五种蛋白质包含JmjC结构域,这是在横跨许多生物的大型组蛋白脱甲基酶家族中发现的标志性基序。最近已确定出芽酵母中的一种含JmjC结构域的蛋白质Jhd1是一种靶向于以二甲基和单甲基状态修饰的H3K36的组蛋白脱甲基酶。在这里,我们确定了第二个包含JmjC域的组蛋白脱甲基酶Rph1,它可以特异性地脱甲基H3K36三和二甲基修饰状态。令人惊讶的是,Rph1可以去除H3K9甲基化,这是发芽的酵母染色质中未发现的组蛋白修饰。 Rph1使H3K9脱甲基的能力提供了 S的第一个迹象。啤酒可能曾经编码过H3K9甲基化系统,并暗示Rph1是该修饰系统的功能性痕迹。

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