Location, location, and location: compartmentalization of Hedgehog signaling at primary cilia
Primary cilia are solitary, microtubule‐based organelles that serve as signaling hubs for the Hedgehog (Hh) pathway, which regulates embryonic development and adult tissue homeostasis. While protein localization studies have suggested that the dynamic trafficking of Hh components at cilia plays an i...
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description | Primary cilia are solitary, microtubule‐based organelles that serve as signaling hubs for the Hedgehog (Hh) pathway, which regulates embryonic development and adult tissue homeostasis. While protein localization studies have suggested that the dynamic trafficking of Hh components at cilia plays an important role, the molecular basis of Hh signal transduction at cilia is not well understood. In a recent study published in
Nature Cell Biology
(He
et al
, 2014), He and colleagues demonstrate that the kinesin KIF7, a conserved regulator of Hh signaling, limits ciliary length by acting at the plus‐ends of microtubules to both reduce growth rate and increase catastrophe frequency. They propose that this biochemical activity establishes a specialized compartment at the tip of the cilia where the activity the Gli family of Hh transcription factors is regulated.
Graphical Abstract
KIF7 is a conserved kinesin involved in Hh signaling that associates with microtubule plus‐ends in cilia to regulate axonemal stability and length, and to generate a cilia‐tip compartment where Gli proteins processing is regulated. |
doi_str_mv | 10.15252/embj.201489294 |
format | Article |
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Nature Cell Biology
(He
et al
, 2014), He and colleagues demonstrate that the kinesin KIF7, a conserved regulator of Hh signaling, limits ciliary length by acting at the plus‐ends of microtubules to both reduce growth rate and increase catastrophe frequency. They propose that this biochemical activity establishes a specialized compartment at the tip of the cilia where the activity the Gli family of Hh transcription factors is regulated.
Graphical Abstract
KIF7 is a conserved kinesin involved in Hh signaling that associates with microtubule plus‐ends in cilia to regulate axonemal stability and length, and to generate a cilia‐tip compartment where Gli proteins processing is regulated.</description><identifier>ISSN: 0261-4189</identifier><identifier>EISSN: 1460-2075</identifier><identifier>DOI: 10.15252/embj.201489294</identifier><identifier>PMID: 25037564</identifier><identifier>CODEN: EMJODG</identifier><language>eng</language><publisher>London: Blackwell Publishing Ltd</publisher><subject>Animals ; Biochemistry ; Cellular biology ; Cilia - metabolism ; EMBO05 ; EMBO37 ; Embryonic growth stage ; Have You Seen? ; Hedgehog Proteins - metabolism ; Humans ; Kinesin - metabolism ; Molecular biology ; Signal Transduction ; Transcription factors</subject><ispartof>The EMBO journal, 2014-09, Vol.33 (17), p.1852-1854</ispartof><rights>The Authors 2014</rights><rights>2014 The Authors</rights><rights>2014 EMBO</rights><rights>2014 The Authors 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5514-9c7c74b0338d9ecb999ba60d5b6ff03d6e2ab0ee21d6f90a92014cfbcefc97e63</citedby><cites>FETCH-LOGICAL-c5514-9c7c74b0338d9ecb999ba60d5b6ff03d6e2ab0ee21d6f90a92014cfbcefc97e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195781/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195781/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,1433,27924,27925,41120,42189,45574,45575,46409,46833,51576,53791,53793</link.rule.ids><linktorsrc>$$Uhttps://doi.org/10.15252/embj.201489294$$EView_record_in_Springer_Nature$$FView_record_in_$$GSpringer_Nature</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25037564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pusapati, Ganesh V</creatorcontrib><creatorcontrib>Rohatgi, Rajat</creatorcontrib><title>Location, location, and location: compartmentalization of Hedgehog signaling at primary cilia</title><title>The EMBO journal</title><addtitle>EMBO J</addtitle><addtitle>EMBO J</addtitle><description>Primary cilia are solitary, microtubule‐based organelles that serve as signaling hubs for the Hedgehog (Hh) pathway, which regulates embryonic development and adult tissue homeostasis. While protein localization studies have suggested that the dynamic trafficking of Hh components at cilia plays an important role, the molecular basis of Hh signal transduction at cilia is not well understood. In a recent study published in
Nature Cell Biology
(He
et al
, 2014), He and colleagues demonstrate that the kinesin KIF7, a conserved regulator of Hh signaling, limits ciliary length by acting at the plus‐ends of microtubules to both reduce growth rate and increase catastrophe frequency. They propose that this biochemical activity establishes a specialized compartment at the tip of the cilia where the activity the Gli family of Hh transcription factors is regulated.
Graphical Abstract
KIF7 is a conserved kinesin involved in Hh signaling that associates with microtubule plus‐ends in cilia to regulate axonemal stability and length, and to generate a cilia‐tip compartment where Gli proteins processing is regulated.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Cellular biology</subject><subject>Cilia - metabolism</subject><subject>EMBO05</subject><subject>EMBO37</subject><subject>Embryonic growth stage</subject><subject>Have You Seen?</subject><subject>Hedgehog Proteins - metabolism</subject><subject>Humans</subject><subject>Kinesin - metabolism</subject><subject>Molecular biology</subject><subject>Signal Transduction</subject><subject>Transcription factors</subject><issn>0261-4189</issn><issn>1460-2075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EokNhzQ5FYtMFaW3HduIukOjQB2gKm6KukOU4N6mHJJ7aGaD99XiaIRqQECs_7nePz_VB6CXBh4RTTo-gK5eHFBNWSCrZIzQjTOCU4pw_RjNMBUkZKeQeehbCEmPMi5w8RXuU4yzngs3Q14UzerCuf5O000731XQ6TozrVtoPHfSDbu39w23i6uQCqgZuXJME2_Sx0jeJHpKVt532d4mxrdXP0ZNatwFebNd99OXs9Gp-kS4-n3-Yv1ukhnPCUmlyk7MSZ1lRSTCllLLUAle8FHWNs0oA1SUGoKQStcRabgY2dWmgNjIHke2jt6Pual12UJlo1etWbb0op636s9LbG9W474oRyfOCRIGDrYB3t2sIg-psMNC2uge3DopwLgUpKMERff0XunRrHz9gQwlBeMZlHqmjkTLeheChnswQrB6iU5vo1BRd7Hi1O8PE_84qAscj8MO2cPc_PXV6efJxVx2PzSH29Q34Hdf_NJSOLTYM8HN6T_tvSuTRkrr-dK7eX7MTejXH6jL7BVmvxv4</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Pusapati, Ganesh V</creator><creator>Rohatgi, Rajat</creator><general>Blackwell Publishing Ltd</general><general>Nature Publishing Group UK</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140901</creationdate><title>Location, location, and location: compartmentalization of Hedgehog signaling at primary cilia</title><author>Pusapati, Ganesh V ; 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While protein localization studies have suggested that the dynamic trafficking of Hh components at cilia plays an important role, the molecular basis of Hh signal transduction at cilia is not well understood. In a recent study published in
Nature Cell Biology
(He
et al
, 2014), He and colleagues demonstrate that the kinesin KIF7, a conserved regulator of Hh signaling, limits ciliary length by acting at the plus‐ends of microtubules to both reduce growth rate and increase catastrophe frequency. They propose that this biochemical activity establishes a specialized compartment at the tip of the cilia where the activity the Gli family of Hh transcription factors is regulated.
Graphical Abstract
KIF7 is a conserved kinesin involved in Hh signaling that associates with microtubule plus‐ends in cilia to regulate axonemal stability and length, and to generate a cilia‐tip compartment where Gli proteins processing is regulated.</abstract><cop>London</cop><pub>Blackwell Publishing Ltd</pub><pmid>25037564</pmid><doi>10.15252/embj.201489294</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biochemistry Cellular biology Cilia - metabolism EMBO05 EMBO37 Embryonic growth stage Have You Seen? Hedgehog Proteins - metabolism Humans Kinesin - metabolism Molecular biology Signal Transduction Transcription factors |
title | Location, location, and location: compartmentalization of Hedgehog signaling at primary cilia |
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