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1.
Nat Commun ; 15(1): 4316, 2024 May 21.
Article in English | MEDLINE | ID: mdl-38773095

ABSTRACT

As signalling organelles, cilia regulate their G protein-coupled receptor content by ectocytosis, a process requiring localised actin dynamics to alter membrane shape. Photoreceptor outer segments comprise an expanse of folded membranes (discs) at the tip of highly-specialised connecting cilia, into which photosensitive GPCRs are concentrated. Discs are shed and remade daily. Defects in this process, due to mutations, cause retinitis pigmentosa (RP). Whilst fundamental for vision, the mechanism of photoreceptor disc generation is poorly understood. Here, we show membrane deformation required for disc genesis is driven by dynamic actin changes in a process akin to ectocytosis. We show RPGR, a leading RP gene, regulates actin-binding protein activity central to this process. Actin dynamics, required for disc formation, are perturbed in Rpgr mouse models, leading to aborted membrane shedding as ectosome-like vesicles, photoreceptor death and visual loss. Actin manipulation partially rescues this, suggesting the pathway could be targeted therapeutically. These findings help define how actin-mediated dynamics control outer segment turnover.


Subject(s)
Actins , Eye Proteins , Retinitis Pigmentosa , Animals , Actins/metabolism , Mice , Retinitis Pigmentosa/metabolism , Retinitis Pigmentosa/genetics , Eye Proteins/metabolism , Eye Proteins/genetics , Cilia/metabolism , Humans , Retinal Photoreceptor Cell Outer Segment/metabolism , Mice, Knockout , Mice, Inbred C57BL , Cell Membrane/metabolism
2.
Science ; 384(6694): eadf5489, 2024 Apr 26.
Article in English | MEDLINE | ID: mdl-38662826

ABSTRACT

Tubulin, one of the most abundant cytoskeletal building blocks, has numerous isotypes in metazoans encoded by different conserved genes. Whether these distinct isotypes form cell type- and context-specific microtubule structures is poorly understood. Based on a cohort of 12 patients with primary ciliary dyskinesia as well as mouse mutants, we identified and characterized variants in the TUBB4B isotype that specifically perturbed centriole and cilium biogenesis. Distinct TUBB4B variants differentially affected microtubule dynamics and cilia formation in a dominant-negative manner. Structure-function studies revealed that different TUBB4B variants disrupted distinct tubulin interfaces, thereby enabling stratification of patients into three classes of ciliopathic diseases. These findings show that specific tubulin isotypes have distinct and nonredundant subcellular functions and establish a link between tubulinopathies and ciliopathies.


Subject(s)
Axoneme , Centrioles , Cilia , Ciliary Motility Disorders , Tubulin , Animals , Humans , Mice , Axoneme/metabolism , Centrioles/metabolism , Cilia/metabolism , Ciliary Motility Disorders/genetics , Ciliary Motility Disorders/metabolism , Mutation , Protein Isoforms/genetics , Protein Isoforms/metabolism , Tubulin/genetics , Tubulin/metabolism , Male , Female , Mice, Knockout
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