Cargando…
The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells
Wnt and Netrin signaling regulate diverse essential functions. Using a genetic approach combined with temporal gene expression analysis, we found a regulatory link between the Wnt receptor MOM-5/Frizzled and the UNC-6/Netrin receptor UNC-5. These two receptors play key roles in guiding cell and axon...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546399/ https://www.ncbi.nlm.nih.gov/pubmed/26292279 http://dx.doi.org/10.1371/journal.pgen.1005446 |
_version_ | 1782386920440987648 |
---|---|
author | Levy-Strumpf, Naomi Krizus, Meghan Zheng, Hong Brown, Louise Culotti, Joseph G. |
author_facet | Levy-Strumpf, Naomi Krizus, Meghan Zheng, Hong Brown, Louise Culotti, Joseph G. |
author_sort | Levy-Strumpf, Naomi |
collection | PubMed |
description | Wnt and Netrin signaling regulate diverse essential functions. Using a genetic approach combined with temporal gene expression analysis, we found a regulatory link between the Wnt receptor MOM-5/Frizzled and the UNC-6/Netrin receptor UNC-5. These two receptors play key roles in guiding cell and axon migrations, including the migration of the C. elegans Distal Tip Cells (DTCs). DTCs migrate post-embryonically in three sequential phases: in the first phase along the Antero-Posterior (A/P) axis, in the second, along the Dorso-Ventral (D/V) axis, and in the third, along the A/P axis. Loss of MOM-5/Frizzled function causes third phase A/P polarity reversals of the migrating DTCs. We show that an over-expression of UNC-5 causes similar DTC A/P polarity reversals and that unc-5 deficits markedly suppress the A/P polarity reversals caused by mutations in mom-5/frizzled. This implicates MOM-5/Frizzled as a negative regulator of unc-5. We provide further evidence that small GTPases mediate MOM-5’s regulation of unc-5 such that one outcome of impaired function of small GTPases like CED-10/Rac and MIG-2/RhoG is an increase in unc-5 function. The work presented here demonstrates the existence of cross talk between components of the Netrin and Wnt signaling pathways and provides further insights into the way guidance signaling mechanisms are integrated to orchestrate directed cell migration. |
format | Online Article Text |
id | pubmed-4546399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45463992015-08-26 The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells Levy-Strumpf, Naomi Krizus, Meghan Zheng, Hong Brown, Louise Culotti, Joseph G. PLoS Genet Research Article Wnt and Netrin signaling regulate diverse essential functions. Using a genetic approach combined with temporal gene expression analysis, we found a regulatory link between the Wnt receptor MOM-5/Frizzled and the UNC-6/Netrin receptor UNC-5. These two receptors play key roles in guiding cell and axon migrations, including the migration of the C. elegans Distal Tip Cells (DTCs). DTCs migrate post-embryonically in three sequential phases: in the first phase along the Antero-Posterior (A/P) axis, in the second, along the Dorso-Ventral (D/V) axis, and in the third, along the A/P axis. Loss of MOM-5/Frizzled function causes third phase A/P polarity reversals of the migrating DTCs. We show that an over-expression of UNC-5 causes similar DTC A/P polarity reversals and that unc-5 deficits markedly suppress the A/P polarity reversals caused by mutations in mom-5/frizzled. This implicates MOM-5/Frizzled as a negative regulator of unc-5. We provide further evidence that small GTPases mediate MOM-5’s regulation of unc-5 such that one outcome of impaired function of small GTPases like CED-10/Rac and MIG-2/RhoG is an increase in unc-5 function. The work presented here demonstrates the existence of cross talk between components of the Netrin and Wnt signaling pathways and provides further insights into the way guidance signaling mechanisms are integrated to orchestrate directed cell migration. Public Library of Science 2015-08-20 /pmc/articles/PMC4546399/ /pubmed/26292279 http://dx.doi.org/10.1371/journal.pgen.1005446 Text en © 2015 Levy-Strumpf et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Levy-Strumpf, Naomi Krizus, Meghan Zheng, Hong Brown, Louise Culotti, Joseph G. The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
title | The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
title_full | The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
title_fullStr | The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
title_full_unstemmed | The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
title_short | The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
title_sort | wnt frizzled receptor mom-5 regulates the unc-5 netrin receptor through small gtpase-dependent signaling to determine the polarity of migrating cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546399/ https://www.ncbi.nlm.nih.gov/pubmed/26292279 http://dx.doi.org/10.1371/journal.pgen.1005446 |
work_keys_str_mv | AT levystrumpfnaomi thewntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT krizusmeghan thewntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT zhenghong thewntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT brownlouise thewntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT culottijosephg thewntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT levystrumpfnaomi wntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT krizusmeghan wntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT zhenghong wntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT brownlouise wntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells AT culottijosephg wntfrizzledreceptormom5regulatestheunc5netrinreceptorthroughsmallgtpasedependentsignalingtodeterminethepolarityofmigratingcells |