Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

Nature Genetics
Fedik RahimovJeffrey C Murray


Previously we have shown that nonsyndromic cleft lip with or without cleft palate (NSCL/P) is strongly associated with SNPs in IRF6 (interferon regulatory factor 6). Here, we use multispecies sequence comparisons to identify a common SNP (rs642961, G>A) in a newly identified IRF6 enhancer. The A allele is significantly overtransmitted (P = 1 x 10(-11)) in families with NSCL/P, in particular those with cleft lip but not cleft palate. Further, there is a dosage effect of the A allele, with a relative risk for cleft lip of 1.68 for the AG genotype and 2.40 for the AA genotype. EMSA and ChIP assays demonstrate that the risk allele disrupts the binding site of transcription factor AP-2alpha and expression analysis in the mouse localizes the enhancer activity to craniofacial and limb structures. Our findings place IRF6 and AP-2alpha in the same developmental pathway and identify a high-frequency variant in a regulatory element contributing substantially to a common, complex disorder.


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Related Concepts

Biochemical Pathway
Conserved Sequence
Interferon Regulatory Factors
Transcription Factor AP-2 Alpha
Cognitive Complexity
NHLH1 gene
Odds Ratio
Chromatin Immunoprecipitation
Plasma Protein Binding Capacity
Limb Structure

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