Cargando…
Multiple ciliary localization signals control INPP5E ciliary targeting
Primary cilia are sensory membrane protrusions whose dysfunction causes ciliopathies. INPP5E is a ciliary phosphoinositide phosphatase mutated in ciliopathies like Joubert syndrome. INPP5E regulates numerous ciliary functions, but how it accumulates in cilia remains poorly understood. Herein, we sho...
Autores principales: | Cilleros-Rodriguez, Dario, Martin-Morales, Raquel, Barbeito, Pablo, Deb Roy, Abhijit, Loukil, Abdelhalim, Sierra-Rodero, Belen, Herranz, Gonzalo, Pampliega, Olatz, Redrejo-Rodriguez, Modesto, Goetz, Sarah C, Izquierdo, Manuel, Inoue, Takanari, Garcia-Gonzalo, Francesc R |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444247/ https://www.ncbi.nlm.nih.gov/pubmed/36063381 http://dx.doi.org/10.7554/eLife.78383 |
Ejemplares similares
-
A recombinant BBSome core complex and how it interacts with ciliary cargo
por: Klink, Björn Udo, et al.
Publicado: (2017) -
Targeting an anchored phosphatase-deacetylase unit restores renal ciliary homeostasis
por: Gopalan, Janani, et al.
Publicado: (2021) -
Disrupting the ciliary gradient of active Arl3 affects rod photoreceptor nuclear migration
por: Travis, Amanda M, et al.
Publicado: (2023) -
A complex of distal appendage–associated kinases linked to human disease regulates ciliary trafficking and stability
por: Loukil, Abdelhalim, et al.
Publicado: (2021) -
Interaction of INPP5E with ARL13B is essential for its ciliary membrane retention but dispensable for its ciliary entry
por: Qiu, Hantian, et al.
Publicado: (2021)