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Hedgehog Signal and Genetic Disorders.

作者信息

Sasai Noriaki, Toriyama Michinori, Kondo Toru

机构信息

Developmental Biomedical Science, Division of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Japan.

Systems Neurobiology and Medicine, Division of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Japan.

出版信息

Front Genet. 2019 Nov 8;10:1103. doi: 10.3389/fgene.2019.01103. eCollection 2019.


DOI:10.3389/fgene.2019.01103
PMID:31781166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6856222/
Abstract

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/580d/6856222/4ea59e69485f/fgene-10-01103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/580d/6856222/4ea59e69485f/fgene-10-01103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/580d/6856222/4ea59e69485f/fgene-10-01103-g001.jpg

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本文引用的文献

[1]
GPR17 is an essential regulator for the temporal adaptation of sonic hedgehog signalling in neural tube development.

Development. 2019-9-12

[2]
Phase I and phase II sonidegib and vismodegib clinical trials for the treatment of paediatric and adult MB patients: a systemic review and meta-analysis.

Acta Neuropathol Commun. 2019-7-30

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Transl Oncol. 2019-10

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Neuron. 2019-5-1

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Front Genet. 2019-2-12

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Targeting the Oncoprotein Smoothened by Small Molecules: Focus on Novel Acylguanidine Derivatives as Potent Smoothened Inhibitors.

Cells. 2018-12-14

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Progress and potential in organoid research.

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Amyloid-β interrupts canonical Sonic hedgehog signaling by distorting primary cilia structure.

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