Cargando…

A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis

Primary cilia are sensory antennae crucial for cell and organism development, and defects in their biogenesis cause ciliopathies. Ciliogenesis involves membrane trafficking mediated by small guanosine triphosphatases (GTPases) including Rabs, molecular switches activated by guanine nucleotide exchan...

Descripción completa

Detalles Bibliográficos
Autores principales: Kumar, Rahul, Francis, Vincent, Kulasekaran, Gopinath, Khan, Maleeha, Armstrong, Gary A. B., McPherson, Peter S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865772/
https://www.ncbi.nlm.nih.gov/pubmed/35196081
http://dx.doi.org/10.1126/sciadv.abk3088
_version_ 1784655699787120640
author Kumar, Rahul
Francis, Vincent
Kulasekaran, Gopinath
Khan, Maleeha
Armstrong, Gary A. B.
McPherson, Peter S.
author_facet Kumar, Rahul
Francis, Vincent
Kulasekaran, Gopinath
Khan, Maleeha
Armstrong, Gary A. B.
McPherson, Peter S.
author_sort Kumar, Rahul
collection PubMed
description Primary cilia are sensory antennae crucial for cell and organism development, and defects in their biogenesis cause ciliopathies. Ciliogenesis involves membrane trafficking mediated by small guanosine triphosphatases (GTPases) including Rabs, molecular switches activated by guanine nucleotide exchange factors (GEFs). The largest family of Rab GEFs is the DENN domain–bearing proteins. Here, we screen all 60 Rabs against two major DENN domain families using a cellular GEF assay, uncovering 19 novel DENN/Rab pairs. The screen reveals Rab10 as a substrate for DENND2B, a protein previously implicated in cancer and severe mental retardation. Through activation of Rab10, DENND2B represses the formation of primary cilia. Through a second pathway, DENND2B functions as a GEF for RhoA to control the length of primary cilia. This work thus identifies an unexpected diversity in DENN domain–mediated activation of Rabs, a previously unidentified non-Rab substrate for a DENN domain, and a new regulatory protein in primary ciliogenesis.
format Online
Article
Text
id pubmed-8865772
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-88657722022-03-10 A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis Kumar, Rahul Francis, Vincent Kulasekaran, Gopinath Khan, Maleeha Armstrong, Gary A. B. McPherson, Peter S. Sci Adv Biomedicine and Life Sciences Primary cilia are sensory antennae crucial for cell and organism development, and defects in their biogenesis cause ciliopathies. Ciliogenesis involves membrane trafficking mediated by small guanosine triphosphatases (GTPases) including Rabs, molecular switches activated by guanine nucleotide exchange factors (GEFs). The largest family of Rab GEFs is the DENN domain–bearing proteins. Here, we screen all 60 Rabs against two major DENN domain families using a cellular GEF assay, uncovering 19 novel DENN/Rab pairs. The screen reveals Rab10 as a substrate for DENND2B, a protein previously implicated in cancer and severe mental retardation. Through activation of Rab10, DENND2B represses the formation of primary cilia. Through a second pathway, DENND2B functions as a GEF for RhoA to control the length of primary cilia. This work thus identifies an unexpected diversity in DENN domain–mediated activation of Rabs, a previously unidentified non-Rab substrate for a DENN domain, and a new regulatory protein in primary ciliogenesis. American Association for the Advancement of Science 2022-02-23 /pmc/articles/PMC8865772/ /pubmed/35196081 http://dx.doi.org/10.1126/sciadv.abk3088 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Kumar, Rahul
Francis, Vincent
Kulasekaran, Gopinath
Khan, Maleeha
Armstrong, Gary A. B.
McPherson, Peter S.
A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis
title A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis
title_full A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis
title_fullStr A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis
title_full_unstemmed A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis
title_short A cell-based GEF assay reveals new substrates for DENN domains and a role for DENND2B in primary ciliogenesis
title_sort cell-based gef assay reveals new substrates for denn domains and a role for dennd2b in primary ciliogenesis
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865772/
https://www.ncbi.nlm.nih.gov/pubmed/35196081
http://dx.doi.org/10.1126/sciadv.abk3088
work_keys_str_mv AT kumarrahul acellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT francisvincent acellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT kulasekarangopinath acellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT khanmaleeha acellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT armstronggaryab acellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT mcphersonpeters acellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT kumarrahul cellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT francisvincent cellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT kulasekarangopinath cellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT khanmaleeha cellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT armstronggaryab cellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis
AT mcphersonpeters cellbasedgefassayrevealsnewsubstratesfordenndomainsandarolefordennd2binprimaryciliogenesis