Drosophila Dosage Compensation Involves Enhanced Pol II Recruitment to Male X-Linked Promoters

被引:59
作者
Conrad, Thomas [2 ]
Cavalli, Florence M. G. [1 ]
Vaquerizas, Juan M. [1 ]
Luscombe, Nicholas M. [1 ,3 ,4 ,5 ]
Akhtar, Asifa [2 ]
机构
[1] EMBL European Bioinformat Inst, Cambridge CB10 1SD, England
[2] Max Planck Inst Immunobiol & Epigenet, D-79108 Freiburg, Germany
[3] Okinawa Inst Sci & Technol, Onna Son, Okinawa 9040495, Japan
[4] Canc Res UK, London Res Inst, Lincolns Inn Fields 44, London WC2A 3LY, England
[5] UCL, UCL Genet Inst, Dept Genet Evolut & Environm, London WC1E 6BT, England
关键词
MSL COMPLEX; H4K16; ACETYLATION; RNA-POLYMERASE; CHROMOSOME; MELANOGASTER; GENOME; GENES; TRANSCRIPTION; EXPRESSION; MOF;
D O I
10.1126/science.1221428
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Through hyperacetylation of histone H4 lysine 16 (H4K16), the male-specific lethal (MSL) complex in Drosophila approximately doubles transcription from the single male X chromosome in order to match X-linked expression in females and expression from diploid autosomes. By obtaining accurate measurements of RNA polymerase II (Pol II) occupancies and short promoter-proximal RNA production, we detected a consistent, genome-scale increase in Pol II activity at the promoters of male X-linked genes. Moreover, we found that enhanced Pol II recruitment to male X-linked promoters is largely dependent on the MSL complex. These observations provide insights into how global modulation of chromatin structure by histone acetylation contributes to the precise control of Pol II function.
引用
收藏
页码:742 / 746
页数:5
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