Cloning and genetic mapping of zebrafish BMP-2

被引:0
|
作者
Lee, KH
Marden, JJ
Thompson, MS
MacLennan, H
Kishimoto, Y
Pratt, SJ
Schulte-Merker, S
Hammerschmidt, M
Johnson, SL
Postlethwaite, JH
Beier, DC
Zon, LI
机构
[1] Childrens Hosp, Howard Hughes Med Inst, Div Hematol Oncol, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Cardiol, Boston, MA 02115 USA
[3] MPI Entwicklungsbiol, Tubingen, Germany
[4] MPI Immunobiol, Spemann Labs, Freiburg, Germany
[5] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[6] Univ Oregon, Inst Neurosci, Eugene, OR 97403 USA
[7] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Genet, Boston, MA 02115 USA
来源
DEVELOPMENTAL GENETICS | 1998年 / 23卷 / 02期
关键词
bone morphogenetic protein; zebrafish; genetics;
D O I
10.1002/(SICI)1520-6408(1998)23:2<97::AID-DVG1>3.3.CO;2-2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The BMP family of polypeptide growth factors has been shown to play diverse roles in establishing embryonic patterning and tissue fates. We report the cloning of the zebrafish homologue of BMP-2, examine its expression during embryogenesis, and find that it is localized to the distal end of the long arm of zebrafish chromosome 20. A missense mutation of the bmp2 gene has recently been shown to be responsible for the early dorsalized phenotype of the zebrafish swirl mutant [Kishimoto et al., 1997]. Given the dynamic expression of bmp2 in the developing embryo and the complex interactions of BMP signaling response in vertebrates, it is possible that other mutant phenotypes, due to altered bmp2 gene expression, will eventually map to or interact with this genetic locus. Dev. Genet. 23:97-103, 1998. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:97 / 103
页数:7
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