In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading

被引:194
作者
Knight, JC [1 ]
Keating, BJ
Rockett, KA
Kwiatkowski, DR
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[2] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[3] Univ Oxford, John Radcliffe Hosp, Dept Pediat, Oxford OX3 9DU, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/ng1124
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In vivo characterization of regulatory polymorphisms is a key requirement for next-generation human genetic analysis. Here we describe haploChIP, a method that uses chromatin immunoprecipitation (ChIP) and mass spectrometry to identify differential protein-DNA binding in vivo associated with allelic variants of a gene. We demonstrate this approach with the imprinted gene SNRPN. HaploChIP showed close correlation between the level of bound phosphorylated RNA polymerase II at the SNRPN locus and allele-specific expression. Application of the approach to the TNF/LTA locus identified functionally important haplotypes that correlate with allele-specific transcription of LTA. The haploChIP method may be useful in high-throughput screening for common DNA polymorphisms that affect gene regulation in vivo.
引用
收藏
页码:469 / 475
页数:7
相关论文
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