Regulation of Jumonji-domain-containing histone demethylases by hypoxia-inducible factor (HIF)-1α

被引:244
作者
Pollard, Patrick J. [1 ]
Loenarz, Christoph [2 ,3 ]
Mole, David R. [1 ]
McDonough, Michael A. [2 ,3 ]
Gleadle, Jonathan M. [4 ,5 ]
Schofield, Christopher J. [2 ,3 ]
Ratcliffe, Peter J. [1 ]
机构
[1] Univ Oxford, Oxford OX3 7BN, England
[2] Univ Oxford, Chem Res Lab, Oxford OX1 3TA, England
[3] Univ Oxford, Oxford Ctr Integrat Syst Biol, Oxford OX1 3TA, England
[4] Flinders Univ S Australia, Dept Med, Bedford Pk, SA 5042, Australia
[5] Flinders Med Ctr, Bedford Pk, SA 5042, Australia
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
histone demethylase; hypoxia; hypoxia-inducible factor 1 (HIF-1); Jumonji domain; promoter; transcription factor;
D O I
10.1042/BJ20081238
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transcription factor HIF (hypoxia-inducible factor) mediates a highly pleiotrophic response to hypoxia. Many recent Studies have focused on defining the extent of this transcriptional response. In the present study we have analysed regulation by hypoxia among transcripts encoding human Fe(II)- and 2-oxoglutarate-dependent oxygenases. Our results show that many of these genes are regulated by hypoxia and define two groups of histone demethylases as new classes of hypoxia-regulated genes. Patterns of induction were consistent across a range of cell lines with JMJD1A (where JMJD is Jumonji-domain containing) and JMJD2B demonstrating robust, and JMJD2C more modest, up-regulation by hypoxia. Functional genetic and chromatin immunoprecipitation studies demonstrated the importance of HIF-1 alpha in mediating these responses. Given the importance of historic methylation status in defining patterns of gene expression under different physiological and pathophysiological conditions, these findings predict a role for the HIF system in epigenetic regulation.
引用
收藏
页码:387 / 394
页数:8
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