Vertebrate homologue of Drosophila GAGA factor
Journal of molecular biology, 2010•Elsevier
Polycomb group (PcG) and trithorax group (trxG) proteins are chromatin-mediated regulators
of a number of developmentally important genes including the homeotic genes. In
Drosophila melanogaster, one of the trxG members, Trithorax like (Trl), encodes the
essential multifunctional DNA binding protein called GAGA factor (GAF). While most of the
PcG and trxG genes are conserved from flies to humans, a Trl-GAF homologue has been
conspicuously missing in vertebrates. Here, we report the first identification of c-Krox/Th …
of a number of developmentally important genes including the homeotic genes. In
Drosophila melanogaster, one of the trxG members, Trithorax like (Trl), encodes the
essential multifunctional DNA binding protein called GAGA factor (GAF). While most of the
PcG and trxG genes are conserved from flies to humans, a Trl-GAF homologue has been
conspicuously missing in vertebrates. Here, we report the first identification of c-Krox/Th …
Polycomb group (PcG) and trithorax group (trxG) proteins are chromatin-mediated regulators of a number of developmentally important genes including the homeotic genes. In Drosophila melanogaster, one of the trxG members, Trithorax like (Trl), encodes the essential multifunctional DNA binding protein called GAGA factor (GAF). While most of the PcG and trxG genes are conserved from flies to humans, a Trl-GAF homologue has been conspicuously missing in vertebrates. Here, we report the first identification of c-Krox/Th-POK as the vertebrate homologue of GAF on the basis of sequence similarity and comparative structural analysis. The in silico structural analysis of the zinc finger region showed preferential interaction of vertebrate GAF with GAGA sites similar to that of fly GAF. We also show by cross-immunoreactivity studies that both fly and vertebrate GAFs are highly conserved and share a high degree of structural similarity. Electrophoretic mobility shift assays show that vertebrate GAF binds to GAGA sites in vitro. Finally, in vivo studies by chromatin immunoprecipitation confirmed that vertebrate GAF binds to GAGA-rich DNA sequences present in hox clusters. Identification of vertebrate GAF and the presence of its target sites at various developmentally regulated loci, including hox complexes, highlight the evolutionarily conserved components involved in developmental mechanisms across the evolutionary lineage and answer a long-standing question of the presence of vertebrate GAF.
Elsevier
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