Dual roles for patched in sequestering and transducing hedgehog

被引:760
作者
Chen, Y
Struhl, G
机构
[1] Howard Hughes Medical Institute, Dept. of Genetics and Development, Columbia Univ. Coll. of Phys. and S., New York
关键词
D O I
10.1016/S0092-8674(00)81374-4
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
Secreted proteins of the Hedgehog (Hh) family have diverse organizing roles in animal development. Recently, a serpentine protein Smoothened (Smo) has been proposed as a Hh receptor. Here, we present evidence that implicates another multiple-pass transmembrane protein, Patched (Ptc), in Hh reception and suggests a novel signal transduction mechanism in which Hh binds to Ptc, or a Ptc-Smo complex, and thereby induces Smo activity. Our results also show that Ptc limits the range of Hh action; we provide evidence that high levels of Ptc induced by Hh serve to sequester any free Hh and therefore create a barrier to its further movement.
引用
收藏
页码:553 / 563
页数:11
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