ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies

Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia basal body in epidermal cells, interacts with the ci...

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Autores principales: Hyun-Sook Park, Eirini Papanastasi, Gabriela Blanchard, Elena Chiticariu, Daniel Bachmann, Markus Plomann, Fanny Morice-Picard, Pierre Vabres, Asma Smahi, Marcel Huber, Christine Pich, Daniel Hohl
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/a0f02e7c75a741a59d63e638f2446851
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spelling oai:doaj.org-article:a0f02e7c75a741a59d63e638f24468512021-12-02T16:57:13ZARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies10.1038/s42003-021-02054-92399-3642https://doaj.org/article/a0f02e7c75a741a59d63e638f24468512021-05-01T00:00:00Zhttps://doi.org/10.1038/s42003-021-02054-9https://doaj.org/toc/2399-3642Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia basal body in epidermal cells, interacts with the cilia machinery, and is needed for proper ciliogenesis.Hyun-Sook ParkEirini PapanastasiGabriela BlanchardElena ChiticariuDaniel BachmannMarkus PlomannFanny Morice-PicardPierre VabresAsma SmahiMarcel HuberChristine PichDaniel HohlNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 4, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Hyun-Sook Park
Eirini Papanastasi
Gabriela Blanchard
Elena Chiticariu
Daniel Bachmann
Markus Plomann
Fanny Morice-Picard
Pierre Vabres
Asma Smahi
Marcel Huber
Christine Pich
Daniel Hohl
ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
description Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia basal body in epidermal cells, interacts with the cilia machinery, and is needed for proper ciliogenesis.
format article
author Hyun-Sook Park
Eirini Papanastasi
Gabriela Blanchard
Elena Chiticariu
Daniel Bachmann
Markus Plomann
Fanny Morice-Picard
Pierre Vabres
Asma Smahi
Marcel Huber
Christine Pich
Daniel Hohl
author_facet Hyun-Sook Park
Eirini Papanastasi
Gabriela Blanchard
Elena Chiticariu
Daniel Bachmann
Markus Plomann
Fanny Morice-Picard
Pierre Vabres
Asma Smahi
Marcel Huber
Christine Pich
Daniel Hohl
author_sort Hyun-Sook Park
title ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
title_short ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
title_full ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
title_fullStr ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
title_full_unstemmed ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
title_sort arp-t1-associated bazex–dupré–christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/a0f02e7c75a741a59d63e638f2446851
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