A gene-centered C. elegans protein-DNA interaction network

被引:162
|
作者
Deplancke, Bart [1 ]
Mukhopadhyay, Arnab
Ao, Wanyuan
Elewa, Ahmed M.
Grove, Christian A.
Martinez, Natalia J.
Sequerra, Reynaldo
Doucette-Stamm, Lynn
Reece-Hoyes, John S.
Hope, Ian A.
Tissenbaum, Heidi A.
Mango, Susan E.
Walhout, Albertha J. M.
机构
[1] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[3] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[4] Univ Utah, Dept Oncol Sci, Salt Lake City, UT 84112 USA
[5] Agencourt Biosci Corp, Beverly, MA 01915 USA
[6] Univ Leeds, Sch Biol, Fac Biol Sci, Inst Integrat & Comparat Biol, Leeds LS2 9JT, W Yorkshire, England
关键词
D O I
10.1016/j.cell.2006.04.038
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
Transcription regulatory networks consist of physical and functional interactions between transcription factors (TFs) and their target genes. The systematic mapping of TF-target gene interactions has been pioneered in unicellular systems, using "TF-centered" methods (e.g., chromatin immunoprecipitation). However, metazoan systems are less amenable to such methods. Here, we used "gene-centered" high-throughput yeast one-hybrid (Y1 H) assays to identify 283 interactions between 72 C. elegans digestive tract gene promoters and 117 proteins. The resulting protein-DNA interaction (PDI) network is highly connected and enriched for TFs that are expressed in the digestive tract. We provide functional annotations for similar to 10% of all worm TFs, many of which were previously uncharacterized, and find ten novel putative TFs, illustrating the power of a gene-centered approach. We provide additional in vivo evidence for multiple PDIs and illustrate how the PDI network provides insights into metazoan differential gene expression at a systems level.
引用
收藏
页码:1193 / 1205
页数:13
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