Hop is an unusual homeobox gene that modulates cardiac development

被引:234
作者
Chen, F
Kook, H
Milewski, R
Gitler, AD
Lu, MM
Li, J
Nazarian, R
Schnepp, R
Jen, K
Biben, C
Runke, G
Mackay, JP
Novotny, J
Schwartz, RJ
Harvey, RP
Mullins, MC
Epstein, JA [1 ]
机构
[1] Univ Penn, Hlth Syst, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Hlth Syst, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[3] Victor Chang Cardiac Res Inst, Darlinghurst, NSW 2010, Australia
[4] Univ New S Wales, Fac Med & Life Sci, Kensington, NSW 2051, Australia
[5] Univ Sydney, Sch Mol & Microbiol Biosci, Sydney, NSW 2006, Australia
[6] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
关键词
D O I
10.1016/S0092-8674(02)00932-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:713 / 723
页数:11
相关论文
共 36 条
[1]   ANALYSIS OF THE DEVELOPMENTAL EFFECTS OF A LETHAL MUTATION IN THE HOUSE MOUSE [J].
AUERBACH, R .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1954, 127 (02) :305-+
[2]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[3]   Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways [J].
Benson, DW ;
Silberbach, GM ;
Kavanaugh-McHugh, A ;
Cottrill, C ;
Zhang, YZ ;
Riggs, S ;
Smalls, O ;
Johnson, MC ;
Watson, MS ;
Seidman, JG ;
Seidman, CE ;
Plowden, J ;
Kugler, JD .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (11) :1567-1573
[4]   DETERMINATION OF THE NUCLEAR-MAGNETIC-RESONANCE SOLUTION STRUCTURE OF AN ANTENNAPEDIA HOMEODOMAIN-DNA COMPLEX [J].
BILLETER, M ;
QIAN, YQ ;
OTTING, G ;
MULLER, M ;
GEHRING, W ;
WUTHRICH, K .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 234 (04) :1084-1094
[5]  
Chen CY, 1996, DEV GENET, V19, P119, DOI 10.1002/(SICI)1520-6408(1996)19:2<119::AID-DVG3>3.0.CO
[6]  
2-C
[7]  
Chen CY, 1996, MOL CELL BIOL, V16, P6372
[8]  
CHEN WS, 1995, ONCOL REP, V2, P5
[9]  
Duboule D., 1994, GUIDEBOOK HOMEOBOX G
[10]   The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors [J].
Durocher, D ;
Charron, F ;
Schwartz, RJ ;
Warren, R ;
Nemer, M .
EMBO JOURNAL, 1997, 16 (18) :5687-5696