Perez-Perri Joel I, Dengler Veronica L, Audetat K Audrey, Pandey Ahwan, Bonner Elizabeth A, Urh Marjeta, Mendez Jacqui, Daniels Danette L, Wappner Pablo, Galbraith Matthew D, Espinosa Joaquín M
Instituto Leloir, 1405 Buenos Aires, Argentina.
Howard Hughes Medical Institute and Department of Molecular, Cellular and Developmental Biology, University of Colorado Boulder, Boulder, CO 80309, USA.
Cell Rep. 2016 Jun 28;16(1):37-47. doi: 10.1016/j.celrep.2016.05.082. Epub 2016 Jun 16.
Hypoxia-inducible factors (HIFs) are critical regulators of the cellular response to hypoxia. Despite their established roles in normal physiology and numerous pathologies, the molecular mechanisms by which they control gene expression remain poorly understood. We report here a conserved role for the TIP60 complex as a HIF1 transcriptional cofactor in Drosophila and human cells. TIP60 (KAT5) is required for HIF1-dependent gene expression in fly cells and embryos and colorectal cancer cells. HIF1A interacts with and recruits TIP60 to chromatin. TIP60 is dispensable for HIF1A association with its target genes but is required for HIF1A-dependent chromatin modification and RNA polymerase II activation in hypoxia. In human cells, global analysis of HIF1A-dependent gene activity reveals that most HIF1A targets require either TIP60, the CDK8-Mediator complex, or both as coactivators for full expression in hypoxia. Thus, HIF1A employs functionally diverse cofactors to regulate different subsets of genes within its transcriptional program.
缺氧诱导因子(HIFs)是细胞对缺氧反应的关键调节因子。尽管它们在正常生理学和众多病理过程中已确立了作用,但其控制基因表达的分子机制仍知之甚少。我们在此报告TIP60复合物在果蝇和人类细胞中作为HIF1转录辅因子的保守作用。TIP60(KAT5)是果蝇细胞、胚胎以及结肠直肠癌细胞中HIF1依赖性基因表达所必需的。HIF1A与TIP60相互作用并将其招募至染色质。TIP60对于HIF1A与其靶基因的结合并非必需,但在缺氧条件下对于HIF1A依赖性染色质修饰和RNA聚合酶II激活是必需的。在人类细胞中,对HIF1A依赖性基因活性的全局分析表明,大多数HIF1A靶基因在缺氧条件下需要TIP60、CDK8-中介体复合物或两者作为共激活因子才能完全表达。因此,HIF1A利用功能多样的辅因子来调节其转录程序中的不同基因子集。