Title of article
Hop Is an Unusual Homeobox Gene that Modulates Cardiac Development
Author/Authors
Fabian Chen، نويسنده , , Hyun-Kook Lim، نويسنده , , Rita Milewski، نويسنده , , Aaron D. Gitler، نويسنده , , Min Min Lu، نويسنده , , Jun Li، نويسنده , , Ronniel Nazarian، نويسنده , , Robert Schnepp، نويسنده , , Kuangyu Jen، نويسنده , , Christine Biben، نويسنده , , Greg Runke، نويسنده , , Joel P. Mackay، نويسنده , , Jiri Novotny، نويسنده , , Robert J. Schwartz، نويسنده , , Richard P. Harvey، نويسنده , , Mary C. Mullins، نويسنده , , Jonathan A. Epstein، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
11
From page
713
To page
723
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.
Journal title
CELL
Serial Year
2002
Journal title
CELL
Record number
1017947
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