TY - JOUR
T1 - Genomic approaches towards finding cis-regulatory modules in animals
AU - Hardison, Ross C.
AU - Taylor, James
N1 - Funding Information:
Support is from US National Institutes of Health grants R01 DK065806, RC2 HG005573 and U54 HG004695 and funds from Emory University to J.T.
PY - 2012/7
Y1 - 2012/7
N2 - Differential gene expression is the fundamental mechanism underlying animal development and cell differentiation. However, it is a challenge to identify comprehensively and accurately the DNA sequences that are required to regulate gene expression: namely, cis-regulatory modules (CRMs). Three major features, either singly or in combination, are used to predict CRMs: clusters of transcription factor binding site motifs, non-coding DNA that is under evolutionary constraint and biochemical marks associated with CRMs, such as histone modifications and protein occupancy. The validation rates for predictions indicate that identifying diagnostic biochemical marks is the most reliable method, and understanding is enhanced by the analysis of motifs and conservation patterns within those predicted CRMs.
AB - Differential gene expression is the fundamental mechanism underlying animal development and cell differentiation. However, it is a challenge to identify comprehensively and accurately the DNA sequences that are required to regulate gene expression: namely, cis-regulatory modules (CRMs). Three major features, either singly or in combination, are used to predict CRMs: clusters of transcription factor binding site motifs, non-coding DNA that is under evolutionary constraint and biochemical marks associated with CRMs, such as histone modifications and protein occupancy. The validation rates for predictions indicate that identifying diagnostic biochemical marks is the most reliable method, and understanding is enhanced by the analysis of motifs and conservation patterns within those predicted CRMs.
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U2 - 10.1038/nrg3242
DO - 10.1038/nrg3242
M3 - Review article
C2 - 22705667
AN - SCOPUS:84863890567
SN - 1471-0056
VL - 13
SP - 469
EP - 483
JO - Nature Reviews Genetics
JF - Nature Reviews Genetics
IS - 7
ER -