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Article: Dishevelled attenuates the repelling activity of Wnt signaling during neurite outgrowth in Caenorhabditis elegans

TitleDishevelled attenuates the repelling activity of Wnt signaling during neurite outgrowth in Caenorhabditis elegans
Authors
KeywordsDishevelled
Wnt
Touch receptor neurons
C. Elegans
Axonal guidance
Issue Date2015
Citation
Proceedings of the National Academy of Sciences of the United States of America, 2015, v. 112, n. 43, p. 13243-13248 How to Cite?
AbstractWnt proteins regulate axonal outgrowth along the anterior-posterior axis, but the intracellular mechanisms that modulate the strength of Wnt signaling in axon guidance are largely unknown. Using the Caenorhabditis elegans mechanosensory PLM neurons, we found that posteriorly enriched LIN-44/Wnt acts as a repellent to promote anteriorly directed neurite outgrowth through the LIN-17/Frizzled receptor, instead of controlling neuronal polarity as previously thought. Dishevelled (Dsh) proteins DSH-1 and MIG-5 redundantly mediate the repulsive activity of the Wnt signals to induce anterior outgrowth, whereas DSH-1 also provides feedback inhibition to attenuate the signaling to allow posterior outgrowth against the Wnt gradient. This inhibitory function of DSH-1, which requires its dishevelled, Egl-10, and pleckstrin (DEP) domain, acts by promoting LIN-17 phosphorylation and is antagonized by planar cell polarity signaling components Van Gogh (VANG-1) and Prickle (PRKL-1). Our results suggest that Dsh proteins both respond to Wnt signals to shape neuronal projections and moderate its activity to fine-tune neuronal morphology.
Persistent Identifierhttp://hdl.handle.net/10722/265676
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZheng, Chaogu-
dc.contributor.authorDiaz-Cuadros, Margarete-
dc.contributor.authorChalfie, Martin-
dc.date.accessioned2018-12-03T01:21:21Z-
dc.date.available2018-12-03T01:21:21Z-
dc.date.issued2015-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America, 2015, v. 112, n. 43, p. 13243-13248-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/265676-
dc.description.abstractWnt proteins regulate axonal outgrowth along the anterior-posterior axis, but the intracellular mechanisms that modulate the strength of Wnt signaling in axon guidance are largely unknown. Using the Caenorhabditis elegans mechanosensory PLM neurons, we found that posteriorly enriched LIN-44/Wnt acts as a repellent to promote anteriorly directed neurite outgrowth through the LIN-17/Frizzled receptor, instead of controlling neuronal polarity as previously thought. Dishevelled (Dsh) proteins DSH-1 and MIG-5 redundantly mediate the repulsive activity of the Wnt signals to induce anterior outgrowth, whereas DSH-1 also provides feedback inhibition to attenuate the signaling to allow posterior outgrowth against the Wnt gradient. This inhibitory function of DSH-1, which requires its dishevelled, Egl-10, and pleckstrin (DEP) domain, acts by promoting LIN-17 phosphorylation and is antagonized by planar cell polarity signaling components Van Gogh (VANG-1) and Prickle (PRKL-1). Our results suggest that Dsh proteins both respond to Wnt signals to shape neuronal projections and moderate its activity to fine-tune neuronal morphology.-
dc.languageeng-
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America-
dc.subjectDishevelled-
dc.subjectWnt-
dc.subjectTouch receptor neurons-
dc.subjectC. Elegans-
dc.subjectAxonal guidance-
dc.titleDishevelled attenuates the repelling activity of Wnt signaling during neurite outgrowth in Caenorhabditis elegans-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1073/pnas.1518686112-
dc.identifier.pmid26460008-
dc.identifier.scopuseid_2-s2.0-84945545639-
dc.identifier.volume112-
dc.identifier.issue43-
dc.identifier.spage13243-
dc.identifier.epage13248-
dc.identifier.eissn1091-6490-
dc.identifier.isiWOS:000363458100047-
dc.identifier.issnl0027-8424-

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