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Identification of 67 histone marks and histone lysine crotonylation as a new type of histone modification

机译:识别67种组蛋白标记和组蛋白赖氨酸巴豆酰化作为一种​​新型的组蛋白修饰

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摘要

We report the identification of 67 previously undescribed histone modifications, increasing the current number of known histone marks by about 70%. We further investigated one of the marks, lysine crotonylation (Kcr), confirming that it represents an evolutionarily-conserved histone posttranslational modification. The unique structure and genomic localization of histone Kcr suggest that it is mechanistically and functionally different from histone lysine acetylation (Kac). Specifically, in both human somatic and mouse male germ cell genomes, histone Kcr marks either active promoters or potential enhancers. In male germinal cells immediately following meiosis, Kcr is enriched on sex chromosomes and specifically marks testis-specific genes, including a significant proportion of X-linked genes that escape sex chromosome inactivation in haploid cells. These results therefore dramatically extend the repertoire of histone PTM sites and designate Kcr as a specific mark of active sex chromosome-linked genes in postmeiotic male germ cells.
机译:我们报告了67个先前未描述的组蛋白修饰的鉴定,使已知组蛋白标记的当前数量增加了约70%。我们进一步研究了标记之一,赖氨酸巴豆酰化(Kcr),确认它代表了进化上保守的组蛋白翻译后修饰。组蛋白Kcr的独特结构和基因组定位表明,其在机制和功能上与组蛋白赖氨酸乙酰化(Kac)不同。具体而言,在人类体细胞和小鼠雄性生殖细胞基因组中,组蛋白Kcr均标记为活性启动子或潜在增强子。在减数分裂后的雄性生殖细胞中,Kcr富集在性染色体上,并特异性标记睾丸特异的基因,包括在单倍体细胞中逃脱性染色体失活的大部分X连锁基因。因此,这些结果极大地扩展了组蛋白PTM位点库,并将Kcr指定为减数分裂后雄性生殖细胞中活跃的性染色体连锁基因的特定标记。

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