An improved map of conserved regulatory sites for Saccharomyces cerevisiae

被引:535
|
作者
MacIsaac, KD
Wang, T
Gordon, DB
Gifford, DK
Stormo, GD
Fraenkel, E
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Comp Sci & Artificial Intelligence Lab, Cambridge, MA 02139 USA
[3] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[4] Agilent Technol, Cambridge, MA 02142 USA
[5] MIT, Biol Engn Div, Cambridge, MA 02139 USA
关键词
D O I
10.1186/1471-2105-7-113
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: The regulatory map of a genome consists of the binding sites for proteins that determine the transcription of nearby genes. An initial regulatory map for S. cerevisiae was recently published using six motif discovery programs to analyze genome-wide chromatin immunoprecipitation data for 203 transcription factors. The programs were used to identify sequence motifs that were likely to correspond to the DNA-binding specificity of the immunoprecipitated proteins. We report improved versions of two conservation-based motif discovery algorithms, PhyloCon and Converge. Using these programs, we create a refined regulatory map for S. cerevisiae by reanalyzing the same chromatin immunoprecipitation data. Results: Applying the same conservative criteria that were applied in the original study, we find that PhyloCon and Converge each separately discover more known specificities than the combination of all six programs in the previous study. Combining the results of PhyloCon and Converge, we discover significant sequence motifs for 36 transcription factors that were previously missed. The new set of motifs identifies 636 more regulatory interactions than the previous one. The new network contains 28% more regulatory interactions among transcription factors, evidence of greater cross-talk between regulators. Conclusion: Combining two complementary computational strategies for conservation-based motif discovery improves the ability to identify the specificity of transcriptional regulators from genome-wide chromatin immunoprecipitation data. The increased sensitivity of these methods significantly expands the map of yeast regulatory sites without the need to alter any of the thresholds for statistical significance. The new map of regulatory sites reveals a more elaborate and complex view of the yeast genetic regulatory network than was observed previously.
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页数:14
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