ARL13B regulates juxtaposed cilia-cilia elongation in BBSome dependent manner in Caenorhabditis elegans

dc.contributor.author Turan, Merve Gul
dc.contributor.author Kantarci, Hanife
dc.contributor.author Cevik, Sebiha
dc.contributor.author Kaplan, Oktay I.
dc.contributor.authorID 0000-0002-0935-1929 en_US
dc.contributor.authorID 0000-0002-8733-0920 en_US
dc.contributor.department AGÜ, Yaşam ve Doğa Bilimleri Fakültesi, Moleküler Biyoloji ve Genetik Bölümü en_US
dc.contributor.institutionauthor Turan, Merve Gul
dc.contributor.institutionauthor Kantarci, Hanife
dc.contributor.institutionauthor Cevik, Sebiha
dc.contributor.institutionauthor Kaplan, Oktay I.
dc.date.accessioned 2025-03-10T08:35:36Z
dc.date.available 2025-03-10T08:35:36Z
dc.date.issued 2025 en_US
dc.description We thank Ferhan Yenisert for her assistance in creating a transgenic strain and Bradley K. Yoder for supplying the plasmid (F16F9.3promoter::GFP, PCP41). Several strains were acquired from the CGC, which is supported by the NIH Office of Research Infrastructure Programs (P40 OD010440), United States. This research was supported by the Health Institutes of Turkey (TUSEB) (Project number: 28555), Turkiye to S.C. en_US
dc.description.abstract The interaction of cilia with various cellular compartments, such as axons, has emerged as a new form of cellular communication. Cilia often extend in proximity to cilia from neighboring cells. However, the mechanisms driving this process termed juxtaposed cilia-cilia elongation (JCE) remain unclear. We use fluorescence-based visualization to study the mechanisms of coordinated cilia elongation in sensory neurons of Caenorhabditis elegans. Conducting a selective gene-based screening strategy reveals that ARL-13/ARL13B and MKS-5/RPGRIP1L are essential for JCE. We demonstrate that ARL-13 modulates JCE independently of cilia length. Loss of NPHP-2/inversin along with HDAC-6 enhances the cilia misdirection phenotype of arl-13 mutants, while disruption of the BBSome complex, but not microtubule components, partially suppresses the JCE defects in arl-13 mutants. We further show changes in the phospholipid compositions in arl-13 mutants. We suggest that ARL-13 contributes to JCE, in part, through the modulation of the ciliary membrane. en_US
dc.description.sponsorship NIH Office of Research Infrastructure Programs, United States P40 OD010440 Health Institutes of Turkey (TUSEB), Turkiye 28555 en_US
dc.identifier.endpage 19 en_US
dc.identifier.issn 2589-0042
dc.identifier.issue 2 en_US
dc.identifier.startpage 1 en_US
dc.identifier.uri https://doi.org/10.1016/j.isci.2025.111791
dc.identifier.uri https://hdl.handle.net/20.500.12573/2441
dc.identifier.volume 28 en_US
dc.language.iso eng en_US
dc.publisher CELL PRESS en_US
dc.relation.isversionof 10.1016/j.isci.2025.111791 en_US
dc.relation.journal ISCIENCE en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject FUNCTIONAL REDUNDANCY en_US
dc.subject TUBULIN TRANSPORT en_US
dc.subject JOUBERT SYNDROME en_US
dc.subject SENSORY CILIA en_US
dc.subject DISEASE GENES en_US
dc.subject PROTEIN en_US
dc.subject CILIOGENESIS en_US
dc.subject MUTATIONS en_US
dc.subject FLAGELLAR en_US
dc.subject BIOGENESIS en_US
dc.title ARL13B regulates juxtaposed cilia-cilia elongation in BBSome dependent manner in Caenorhabditis elegans en_US
dc.type article en_US

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