| Literature DB >> 12297045 |
Fabian Chen1, Hyun Kook, Rita Milewski, Aaron D Gitler, Min Min Lu, Jun Li, Ronniel Nazarian, Robert Schnepp, Kuangyu Jen, Christine Biben, Greg Runke, Joel P Mackay, Jiri Novotny, Robert J Schwartz, Richard P Harvey, Mary C Mullins, Jonathan A Epstein.
Abstract
Hop is a small, divergent homeodomain protein that lacks certain conserved residues required for DNA binding. Hop gene expression initiates early in cardiogenesis and continues in cardiomyocytes throughout embryonic and postnatal development. Genetic and biochemical data indicate that Hop functions directly downstream of Nkx2-5. Inactivation of Hop in mice by homologous recombination results in a partially penetrant embryonic lethal phenotype with severe developmental cardiac defects involving the myocardium. Inhibition of Hop activity in zebrafish embryos likewise disrupts cardiac development and results in severely impaired cardiac function. Hop physically interacts with serum response factor (SRF) and inhibits activation of SRF-dependent transcription by inhibiting SRF binding to DNA. Hop encodes an unusual homeodomain protein that modulates SRF-dependent cardiac-specific gene expression and cardiac development.Entities:
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Year: 2002 PMID: 12297045 DOI: 10.1016/s0092-8674(02)00932-7
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582