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Transient Activation of Meox1 Is an Early Component of the Gene Regulatory Network Downstream of Hoxa2

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Hox genes encode transcription factors that regulate morphogenesis in all animals with bilateral symmetry. Although Hox genes have been extensively studied, their molecular function is not clear in vertebrates, and only a limited number of genes regulated by Hox transcription factors have been identified. Hoxa2 is required for correct development of the second branchial arch, its major domain of expression. We now show that Meox1 is genetically downstream from Hoxa2 and is a direct target. Meox1 expression is downregulated in the second arch of Hoxa2 mouse mutant embryos. In chromatin immunoprecipitation (ChIP), Hoxa2 binds to the Meox1 proximal promoter. Two highly conserved binding sites contained in this sequence are required for Hoxa2-dependent activation of the Meox1 promoter. Remarkably, in the absence of Meox1 and its close homolog Meox2, the second branchial arch develops abnormally and two of the three skeletal elements patterned by Hoxa2 are malformed. Finally, we show that Meox1 can specifically bind the DNA sequences recognized by Hoxa2 on its functional target genes. These results provide new insight into the Hoxa2 regulatory network that controls branchial arch identity.

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Animals Base Sequence Branchial Region Cells, Cultured Embryo, Mammalian Homeodomain Proteins Humans Mice Mice, Transgenic Molecular Sequence Data Mutation Promoter Regions, Genetic Protein Binding Sequence Alignment Gene Expression Regulation, Developmental Gene Regulatory Networks

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Transient Activation of Meox1 Is an Early Component of the Gene Regulatory Network Downstream of Hoxa2 Pavel Kirilenko, Guiyuan He, Baljinder S. Mankoo, Moises Mallo, Richard Jones, and Nicoletta Bobola Mol. Cell. Biol. March 15, 2011 31:6 1301-1308; Accepted manuscript posted online 18 January 2011, doi:10.1128/MCB.00705-10

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American Society for Microbiology

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