Identification of a Hoxc8-regulated transcriptional network in mouse embryo fibroblast cells

被引:45
作者
Lei, Haiyan [1 ]
Juan, Aster H. [1 ]
Kim, Moo-Sang [1 ]
Ruddle, Frank H. [1 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
关键词
cancer; chromatin immunoprecipitation; Hox protein binding sites; microarray; PROSTATE-CANCER CELLS; EPITHELIUM-DERIVED FACTOR; ZINC-FINGER PROTEIN; EXPRESSION PATTERN; TUMOR PROGRESSION; HOXC8; EXPRESSION; P53; CYCLE ARREST; HOMEOBOX; GENES;
D O I
10.1073/pnas.0603552103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The transcription factor, Hoxc8, is a member of the homeobox gene family that is vital for growth and differentiation. Previously, we identified 34 genes whose expression levels were changed at least 2-fold by forced expression of Hoxc8 in C57BL/6J mouse embryo fibroblast cells using a mouse 16,463-gene oligonucleotide microarray. In the present study, we used the combined power of microarray profiling, global Hoxc8 DNA-binding site analysis, and high-throughput chromatin immunoprecipitation assays to identify direct and biologically relevant targets of Hoxc8 in vivo. Here we show that 19 of the 34 responsive genes contain Hoxc8 consensus DNA-binding sequence(s) in their regulatory regions. Chromatin immunoprecipitation analysis indicated that Hoxc8-DNA interaction was detected in five of the 19 candidate genes. All of these five target genes have been implicated in oncogenesis, cell adhesion, proliferation, and apoptosis. Overall, the genes described here should aid in the understanding of global regulatory networks of Hox genes and to provide valuable insight into the molecular basis of Hoxc8 in development and carcinogenesis.
引用
收藏
页码:10305 / 10309
页数:5
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