Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA.
Mol Cell Biol. 2012 May;32(9):1710-9. doi: 10.1128/MCB.06546-11. Epub 2012 Mar 5.
Dosage compensation equalizes X-linked gene expression between the sexes. This process is achieved in Caenorhabditis elegans by hermaphrodite-specific, dosage compensation complex (DCC)-mediated, 2-fold X chromosome downregulation. How the DCC downregulates gene expression is not known. By analyzing the distribution of histone modifications in nuclei using quantitative fluorescence microscopy, we found that H4K16 acetylation (H4K16ac) is underrepresented and H4K20 monomethylation (H4K20me1) is enriched on hermaphrodite X chromosomes in a DCC-dependent manner. Depletion of H4K16ac also requires the conserved histone deacetylase SIR-2.1, while enrichment of H4K20me1 requires the activities of the histone methyltransferases SET-1 and SET-4. Our data suggest that the mechanism of dosage compensation in C. elegans involves redistribution of chromatin-modifying activities, leading to a depletion of H4K16ac and an enrichment of H4K20me1 on the X chromosomes. These results support conserved roles for histone H4 chromatin modification in worm dosage compensation analogous to those seen in flies, using similar elements and opposing strategies to achieve differential 2-fold changes in X-linked gene expression.
剂量补偿使雌雄两性的 X 连锁基因表达趋于平衡。在秀丽隐杆线虫中,这一过程是通过雌雄同体特异性、剂量补偿复合物(DCC)介导的、2 倍的 X 染色体下调来实现的。但是,DCC 如何下调基因表达尚不清楚。通过使用定量荧光显微镜分析核内组蛋白修饰的分布,我们发现 H4K16 乙酰化(H4K16ac)的表达减少,H4K20 单甲基化(H4K20me1)在 DCC 依赖性方式下在雌雄同体 X 染色体上富集。H4K16ac 的耗竭也需要保守的组蛋白去乙酰化酶 SIR-2.1,而 H4K20me1 的富集则需要组蛋白甲基转移酶 SET-1 和 SET-4 的活性。我们的数据表明,秀丽隐杆线虫剂量补偿的机制涉及染色质修饰活性的重新分布,导致 H4K16ac 的耗竭和 H4K20me1 在 X 染色体上的富集。这些结果支持了组蛋白 H4 染色质修饰在蠕虫剂量补偿中具有保守作用,类似于在果蝇中观察到的作用,使用类似的元件和相反的策略来实现 X 连锁基因表达的 2 倍差异变化。