共 37 条
ChIP-chip comes of age for genome-wide functional analysis
被引:83
作者:

Wu, Jiejun
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机构: Ohio State Univ, Human Canc Genet Program, Dept Mol Genet, Div Human Canc Genet,Comprehens Canc Ctr, Columbus, OH 43210 USA

Smith, Laura T.
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机构: Ohio State Univ, Human Canc Genet Program, Dept Mol Genet, Div Human Canc Genet,Comprehens Canc Ctr, Columbus, OH 43210 USA

Plass, Christoph
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机构: Ohio State Univ, Human Canc Genet Program, Dept Mol Genet, Div Human Canc Genet,Comprehens Canc Ctr, Columbus, OH 43210 USA

Huang, Tim H-M.
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机构: Ohio State Univ, Human Canc Genet Program, Dept Mol Genet, Div Human Canc Genet,Comprehens Canc Ctr, Columbus, OH 43210 USA
机构:
[1] Ohio State Univ, Human Canc Genet Program, Dept Mol Genet, Div Human Canc Genet,Comprehens Canc Ctr, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Mol Virol, Ctr Comprehens Canc, Div Human Canc Genet, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Immunol, Ctr Comprehens Canc, Div Human Canc Genet, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Med Genet, Ctr Comprehens Canc, Div Human Canc Genet, Columbus, OH 43210 USA
关键词:
D O I:
10.1158/0008-5472.CAN-06-0276
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
In the post-genome era, attention has focused on the functions of genome sequences and how they are regulated. The emerging epigenomic changes and the interactions between cis-acting elements and protein factors may play a central role in gene regulation. To understand the crosstalk between DNA and protein on a genome-ivide scale, one emerging technique, called ChIP-chip, takes the strategy of combining chromatin immunoprecipitation with microarray. This new high-throughput strategy helps screen the targets of critical transcription factors and profile the genome-wide distribution of histone modifications, which will enable the feasibility of conducting a large-scale study, such as the Human Epigenome Project.
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页码:6899 / 6902
页数:4
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