Hedgehog Signal and Genetic Disorders

被引:98
|
作者
Sasai, Noriaki [1 ]
Toriyama, Michinori [2 ,3 ]
Kondo, Toru [4 ]
机构
[1] Nara Inst Sci & Technol, Div Biol Sci, Dev Biomed Sci, Ikoma, Japan
[2] Nara Inst Sci & Technol, Div Biol Sci, Syst Neurobiol & Med, Ikoma, Japan
[3] Kwansel Gakuin Univ, Sch Sci & Technol, Dept Biomed Chem, Sanda, Japan
[4] Hokkaido Univ, Inst Genet Med, Div Stem Cell Biol, Sapporo, Hokkaido, Japan
基金
日本学术振兴会;
关键词
sonic hedgehog (Shh); development; genetic disease; mouse model; ciliopathies; cancer; HEREDITARY MULTIPLE EXOSTOSES; ARREST-SPECIFIC GENE-1; STEROL-SENSING DOMAIN; SONIC-HEDGEHOG; DESERT-HEDGEHOG; CHOLESTEROL MODIFICATION; INDIAN-HEDGEHOG; PRIMARY CILIA; JOUBERT SYNDROME; MOUSE MODEL;
D O I
10.3389/fgene.2019.01103
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The hedgehog (Hh) family comprises sonic hedgehog (Shh), Indian hedgehog (Ihh), and desert hedgehog (Dhh), which are versatile signaling molecules involved in a wide spectrum of biological events including cell differentiation, proliferation, and survival; establishment of the vertebrate body plan; and aging. These molecules play critical roles from embryogenesis to adult stages; therefore, alterations such as abnormal expression or mutations of the genes involved and their downstream factors cause a variety of genetic disorders at different stages. The Hh family involves many signaling mediators and functions through complex mechanisms, and achieving a comprehensive understanding of the entire signaling system is challenging. This review discusses the signaling mediators of the Hh pathway and their functions at the cellular and organismal levels. We first focus on the roles of Hh signaling mediators in signal transduction at the cellular level and the networks formed by these factors. Then, we analyze the spatiotemporal pattern of expression of Hh pathway molecules in tissues and organs, and describe the phenotypes of mutant mice. Finally, we discuss the genetic disorders caused by malfunction of Hh signaling-related molecules in humans.
引用
收藏
页数:23
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