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Article: Microtubule Motors Drive Hedgehog Signaling in Primary Cilia

TitleMicrotubule Motors Drive Hedgehog Signaling in Primary Cilia
Authors
KeywordsHedgehog pathway
dynein
ciliopathies
kinesin
microtubules
primary cilia
Issue Date2017
Citation
Trends in Cell Biology, 2017, v. 27, n. 2, p. 110-125 How to Cite?
AbstractThe mammalian Hedgehog (Hh) signaling pathway is required for development and for maintenance of adult stem cells, and overactivation of the pathway can cause tumorigenesis. All responses to Hh family ligands in mammals require the primary cilium, an ancient microtubule-based organelle that extends from the cell surface. Genetic studies in mice and humans have defined specific functions for cilium-associated microtubule motor proteins: they act in the construction and disassembly of the primary cilium, they control ciliary length and stability, and some have direct roles in mammalian Hh signal transduction. These studies highlight how integrated genetic and cell biological studies can define the molecular mechanisms that underlie cilium-associated health and disease.
Persistent Identifierhttp://hdl.handle.net/10722/298186
ISSN
2021 Impact Factor: 21.167
2020 SCImago Journal Rankings: 8.705
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHe, Mu-
dc.contributor.authorAgbu, Stephanie-
dc.contributor.authorAnderson, Kathryn V.-
dc.date.accessioned2021-04-08T03:07:52Z-
dc.date.available2021-04-08T03:07:52Z-
dc.date.issued2017-
dc.identifier.citationTrends in Cell Biology, 2017, v. 27, n. 2, p. 110-125-
dc.identifier.issn0962-8924-
dc.identifier.urihttp://hdl.handle.net/10722/298186-
dc.description.abstractThe mammalian Hedgehog (Hh) signaling pathway is required for development and for maintenance of adult stem cells, and overactivation of the pathway can cause tumorigenesis. All responses to Hh family ligands in mammals require the primary cilium, an ancient microtubule-based organelle that extends from the cell surface. Genetic studies in mice and humans have defined specific functions for cilium-associated microtubule motor proteins: they act in the construction and disassembly of the primary cilium, they control ciliary length and stability, and some have direct roles in mammalian Hh signal transduction. These studies highlight how integrated genetic and cell biological studies can define the molecular mechanisms that underlie cilium-associated health and disease.-
dc.languageeng-
dc.relation.ispartofTrends in Cell Biology-
dc.subjectHedgehog pathway-
dc.subjectdynein-
dc.subjectciliopathies-
dc.subjectkinesin-
dc.subjectmicrotubules-
dc.subjectprimary cilia-
dc.titleMicrotubule Motors Drive Hedgehog Signaling in Primary Cilia-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1016/j.tcb.2016.09.010-
dc.identifier.pmid27765513-
dc.identifier.pmcidPMC5258846-
dc.identifier.scopuseid_2-s2.0-85005808039-
dc.identifier.volume27-
dc.identifier.issue2-
dc.identifier.spage110-
dc.identifier.epage125-
dc.identifier.eissn1879-3088-
dc.identifier.isiWOS:000393927300003-
dc.identifier.issnl0962-8924-

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