Bayesian network analysis of targeting interactions in chromatin

被引:41
|
作者
van Steensel, Bas [1 ]
Braunschweig, Ulrich [1 ]
Filion, Guillaume J. [1 ]
Chen, Menzies [2 ,3 ]
van Bemmel, Joke G. [1 ]
Ideker, Trey [2 ,3 ]
机构
[1] Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
关键词
POSITION-EFFECT VARIEGATION; GENOME-WIDE ANALYSIS; DROSOPHILA-MELANOGASTER; SACCHAROMYCES-CEREVISIAE; HISTONE DEACETYLASE; GENE-EXPRESSION; DNA; TRANSCRIPTION; COMPLEX; SEGMENTATION;
D O I
10.1101/gr.098822.109
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
In eukaryotes, many chromatin proteins together regulate gene expression. Chromatin proteins often direct the genomic binding pattern of other chromatin proteins, for example, by recruitment or competition mechanisms. The network of such targeting interactions in chromatin is complex and still poorly understood. Based on genome-wide binding maps, we constructed a Bayesian network model of the targeting interactions among a broad set of 43 chromatin components in Drosophila cells. This model predicts many novel functional relationships. For example, we found that the homologous proteins HP1 and HP1C each target the heterochromatin protein HP3 to distinct sets of genes in a competitive manner. We also discovered a central role for the remodeling factor Brahma in the targeting of several DNA-binding factors, including GAGA factor, JRA, and SU(VAR)3-7. Our network model provides a global view of the targeting interplay among dozens of chromatin components.
引用
收藏
页码:190 / 200
页数:11
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