Genetic evidence that Sil is required for the sonic hedgehog response pathway

被引:49
作者
Izraeli, S
Lowe, LA
Bertness, VL
Campaner, S
Hahn, H
Kirsch, IR
Kuehn, MR
机构
[1] NCI, Expt Immunol Branch, Canc Res Ctr, NIH, Bethesda, MD 20892 USA
[2] NCI, Genet Branch, Canc Res Ctr, NIH, Bethesda, MD 20892 USA
[3] GSF, Res Ctr Environm & Hlth, Inst Pathol, Neuherberg, Germany
[4] Chaim Sheba Med Ctr, Dept Pediat Hematol Oncol, IL-52621 Tel Hashomer, Israel
关键词
Sil; sonic hedgehog; patched; signaling; apoptosis;
D O I
10.1002/gene.10004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Sil gene encodes a cytosolic protein required for mouse embryonic midline and left/right axial development. Based on the phenotype of Sil mutant embryos, we hypothesized that Sil may be required for the activity of Sonic Hedgehog (Shh), a secreted signaling molecule also critically important for the development of the embryonic axes and found mutated in multiple types of cancer. Here we tested the genetic interaction between Sil and the Shh pathway by generating and analyzing embryos carrying mutations in both Sil and Patched (Ptch), a Shh receptor that normally inhibits the signaling pathway in the absence of ligand and when mutated leads to constitutive activation of the pathway. We find that Sil(-/-) Ptch(-/-) embryos do not activate the Shh pathway and instead have a phenotype indistinguishable from Sil(-/-) embryos, in which there is a loss of activity of Shh. These results provide genetic evidence that Sil is an essential component of the Shh response, acting downstream to Ptch. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:72 / 77
页数:6
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