Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.

Primary cilia are specialised sensory and developmental signalling devices extending from the surface of most eukaryotic cells. Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiolog...

Full description

Bibliographic Details
Main Authors: Victor L Jensen, Stephen Carter, Anna A W M Sanders, Chunmei Li, Julie Kennedy, Tiffany A Timbers, Jerry Cai, Noemie Scheidel, Breandán N Kennedy, Ryan D Morin, Michel R Leroux, Oliver E Blacque
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-12-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC5145144?pdf=render
_version_ 1819102335371051008
author Victor L Jensen
Stephen Carter
Anna A W M Sanders
Chunmei Li
Julie Kennedy
Tiffany A Timbers
Jerry Cai
Noemie Scheidel
Breandán N Kennedy
Ryan D Morin
Michel R Leroux
Oliver E Blacque
author_facet Victor L Jensen
Stephen Carter
Anna A W M Sanders
Chunmei Li
Julie Kennedy
Tiffany A Timbers
Jerry Cai
Noemie Scheidel
Breandán N Kennedy
Ryan D Morin
Michel R Leroux
Oliver E Blacque
author_sort Victor L Jensen
collection DOAJ
description Primary cilia are specialised sensory and developmental signalling devices extending from the surface of most eukaryotic cells. Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs. Cilium formation, maintenance and function depend on intracellular transport systems such as intraflagellar transport (IFT), which is driven by kinesin-2 and IFT-dynein motors and regulated by the Bardet-Biedl syndrome (BBS) cargo-adaptor protein complex, or BBSome. To identify new cilium-associated genes, we employed the nematode C. elegans, where ciliogenesis occurs within a short timespan during late embryogenesis when most sensory neurons differentiate. Using whole-organism RNA-Seq libraries, we discovered a signature expression profile highly enriched for transcripts of known ciliary proteins, including FAM-161 (FAM161A orthologue), CCDC-104 (CCDC104), and RPI-1 (RP1/RP1L1), which we confirm are cilium-localised in worms. From a list of 185 candidate ciliary genes, we uncover orthologues of human MAP9, YAP, CCDC149, and RAB28 as conserved cilium-associated components. Further analyses of C. elegans RAB-28, recently associated with autosomal-recessive cone-rod dystrophy, reveal that this small GTPase is exclusively expressed in ciliated neurons where it dynamically associates with IFT trains. Whereas inactive GDP-bound RAB-28 displays no IFT movement and diffuse localisation, GTP-bound (activated) RAB-28 concentrates at the periciliary membrane in a BBSome-dependent manner and undergoes bidirectional IFT. Functional analyses reveal that whilst cilium structure, sensory function and IFT are seemingly normal in a rab-28 null allele, overexpression of predicted GDP or GTP locked variants of RAB-28 perturbs cilium and sensory pore morphogenesis and function. Collectively, our findings present a new approach for identifying ciliary proteins, and unveil RAB28, a GTPase most closely related to the BBS protein RABL4/IFT27, as an IFT-associated cargo with BBSome-dependent cell autonomous and non-autonomous functions at the ciliary base.
first_indexed 2024-12-22T01:32:52Z
format Article
id doaj.art-6dd5e2f10a5341d08051a0d2fe967767
institution Directory Open Access Journal
issn 1553-7390
1553-7404
language English
last_indexed 2024-12-22T01:32:52Z
publishDate 2016-12-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj.art-6dd5e2f10a5341d08051a0d2fe9677672022-12-21T18:43:27ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042016-12-011212e100646910.1371/journal.pgen.1006469Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.Victor L JensenStephen CarterAnna A W M SandersChunmei LiJulie KennedyTiffany A TimbersJerry CaiNoemie ScheidelBreandán N KennedyRyan D MorinMichel R LerouxOliver E BlacquePrimary cilia are specialised sensory and developmental signalling devices extending from the surface of most eukaryotic cells. Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs. Cilium formation, maintenance and function depend on intracellular transport systems such as intraflagellar transport (IFT), which is driven by kinesin-2 and IFT-dynein motors and regulated by the Bardet-Biedl syndrome (BBS) cargo-adaptor protein complex, or BBSome. To identify new cilium-associated genes, we employed the nematode C. elegans, where ciliogenesis occurs within a short timespan during late embryogenesis when most sensory neurons differentiate. Using whole-organism RNA-Seq libraries, we discovered a signature expression profile highly enriched for transcripts of known ciliary proteins, including FAM-161 (FAM161A orthologue), CCDC-104 (CCDC104), and RPI-1 (RP1/RP1L1), which we confirm are cilium-localised in worms. From a list of 185 candidate ciliary genes, we uncover orthologues of human MAP9, YAP, CCDC149, and RAB28 as conserved cilium-associated components. Further analyses of C. elegans RAB-28, recently associated with autosomal-recessive cone-rod dystrophy, reveal that this small GTPase is exclusively expressed in ciliated neurons where it dynamically associates with IFT trains. Whereas inactive GDP-bound RAB-28 displays no IFT movement and diffuse localisation, GTP-bound (activated) RAB-28 concentrates at the periciliary membrane in a BBSome-dependent manner and undergoes bidirectional IFT. Functional analyses reveal that whilst cilium structure, sensory function and IFT are seemingly normal in a rab-28 null allele, overexpression of predicted GDP or GTP locked variants of RAB-28 perturbs cilium and sensory pore morphogenesis and function. Collectively, our findings present a new approach for identifying ciliary proteins, and unveil RAB28, a GTPase most closely related to the BBS protein RABL4/IFT27, as an IFT-associated cargo with BBSome-dependent cell autonomous and non-autonomous functions at the ciliary base.http://europepmc.org/articles/PMC5145144?pdf=render
spellingShingle Victor L Jensen
Stephen Carter
Anna A W M Sanders
Chunmei Li
Julie Kennedy
Tiffany A Timbers
Jerry Cai
Noemie Scheidel
Breandán N Kennedy
Ryan D Morin
Michel R Leroux
Oliver E Blacque
Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
PLoS Genetics
title Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
title_full Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
title_fullStr Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
title_full_unstemmed Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
title_short Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
title_sort whole organism developmental expression profiling identifies rab 28 as a novel ciliary gtpase associated with the bbsome and intraflagellar transport
url http://europepmc.org/articles/PMC5145144?pdf=render
work_keys_str_mv AT victorljensen wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT stephencarter wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT annaawmsanders wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT chunmeili wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT juliekennedy wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT tiffanyatimbers wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT jerrycai wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT noemiescheidel wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT breandannkennedy wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT ryandmorin wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT michelrleroux wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport
AT olivereblacque wholeorganismdevelopmentalexpressionprofilingidentifiesrab28asanovelciliarygtpaseassociatedwiththebbsomeandintraflagellartransport