Jelly belly protein activates the receptor tyrosine kinase Alk to specify visceral muscle pioneers

被引:140
作者
Lee, HH
Norris, A
Weiss, JB
Frasch, M
机构
[1] Oregon Hlth Sci Univ, Portland, OR 97201 USA
[2] Mt Sinai Sch Med, Brookdale Dept Mol Cell & Dev Biol, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature01916
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The secreted protein Jelly belly (Jeb) is required for an essential signalling event in Drosophila muscle development. In the absence of functional Jeb, visceral muscle precursors are normally specified but fail to migrate and differentiate(1). The structure and distribution of Jeb protein implies that Jeb functions as a signal to organize the development of visceral muscles(1). Here we show that the Jeb receptor is the Drosophila homologue of anaplastic lymphoma kinase (Alk), a receptor tyrosine kinase of the insulin receptor superfamily. Human ALK was originally identified as a proto-oncogene, but its normal function in mammals is not known(2). In Drosophila, localized Jeb activates Alk and the downstream Ras/mitogen-activated protein kinase cascade to specify a select group of visceral muscle precursors as muscle-patterning pioneers. Jeb/Alk signalling induces the myoblast fusion gene dumbfounded (duf; also known as kirre) as well as org-1, a Drosophila homologue of mammalian TBX1, in these cells.
引用
收藏
页码:507 / 512
页数:6
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