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Genome-wide analysis reveals MOF as a key regulator of dosage compensation and gene expression in Drosophila

机译:全基因组分析表明,MOF是果蝇剂量补偿和基因表达的关键调节剂

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摘要

Dosage compensation, mediated by the MSL complex, regulates X-chromosomal gene expression in Drosophila. Here we report that the histone H4 lysine 16 (H4K16) specific histone acetyltransferase MOF displays differential binding behavior depending on whether the target gene is located on the X chromosome versus the autosomes. More specifically, on the male X chromosome, where MSL1 and MSL3 are preferentially associated with the 30 end of dosage compensated genes, MOF displays a bimodal distribution binding to promoters and the 30 ends of genes. In contrast, on MSL1/MSL3 independent X-linked genes and autosomal genes in males and females, MOF binds primarily to promoters. Binding of MOF to autosomes is functional, as H4K16 acetylation and the transcription levels of a number of genes are affected upon MOF depletion. Therefore, MOF is not only involved in the onset of dosage compensation, but also acts as a regulator of gene expression in the Drosophila genome.
机译:由MSL复合物介导的剂量补偿可调节果蝇中的X染色体基因表达。在这里我们报告说,组蛋白H4赖氨酸16(H4K16)特定的组蛋白乙酰转移酶MOF显示差异结合行为,具体取决于目标基因是否位于X染色体上。更具体地说,在雄性X染色体上,MSL1和MSL3优先与剂量补偿基因的30末端相关,MOF显示出与启动子和基因的30末端结合的双峰分布。相反,在雄性和雌性中,MSL1 / MSL3独立的X连锁基因和常染色体基因上,MOF主要与启动子结合。 MOF与常染色体的结合是功能性的,因为H4K16乙酰化和许多基因的转录水平受MOF消耗的影响。因此,MOF不仅参与剂量补偿的开始,而且还充当果蝇基因组中基因表达的调节剂。

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