Portal de investigación
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
Fecha de publicación:
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Olcese, Chiara
- Patel, Mitali P.
- Shoemark, Amelia
- Kiviluoto, Santeri
- Legendre, Marie
- Williams, Hywel J.
- Vaughan, Cara K.
- Hayward, Jane
- Goldenberg, Alice
- Emes, Richard D.
- Munye, Mustafa M.
- Dyer, Laura
- Cahill, Thomas
- Bevillard, Jeremy
- Gehrig, Corinne
- Guipponi, Michel
- Chantot, Sandra
- Duquesnoy, Philippe
- Thomas, Lucie
- Jeanson, Ludovic
- Copin, Bruno
- Tamalet, Aline
- Thauvin-Robinet, Christel
- Papon, Jean-Francois
- Garin, Antoine
- Pin, Isabelle
- Vera, Gabriella
- Aurora, Paul
- Fassad, Mahmoud R.
- Jenkins, Lucy
- Boustred, Christopher
- Cullup, Thomas
- Dixon, Mellisa
- Onoufriadis, Alexandros
- Bush, Andrew
- Chung, Eddie M. K.
- Antonarakis, Stylianos E.
- Loebinger, Michael R.
- Wilson, Robert
- Escudier, Estelle
- Hogg, Claire
- Amselem, Serge
- Sun, Zhaoxia
- Bartoloni, Lucia
- Blouin, Jean-Louis
- Mitchison, Hannah M.
- UK10K Rare Grp
Grupos
Abstract
By moving essential body fluids and molecules, motile cilia and flagella govern respiratory mucociliary clearance, laterality determination and the transport of gametes and cerebrospinal fluid. Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder frequently caused by non-assembly of dynein arm motors into cilia and flagella axonemes. Before their import into cilia and flagella, multi-subunit axonemal dynein arms are thought to be stabilized and pre-assembled in the cytoplasm through a DNAAF2DNAAF4- HSP90 complex akin to the HSP90 co-chaperone R2TP complex. Here, we demonstrate that large genomic deletions as well as point mutations involving PIH1D3 are responsible for an X-linked form of PCD causing disruption of early axonemal dynein assembly. We propose that PIH1D3, a protein that emerges as a new player of the cytoplasmic pre-assembly pathway, is part of a complementary conserved R2TP-like HSP90 co-chaperone complex, the loss of which affects assembly of a subset of inner arm dyneins.
Datos de la publicación
- ISSN/ISSNe:
- 2041-1723, 2041-1723
- Tipo:
- Article
- Páginas:
- -
- DOI:
- 10.1038/ncomms14279
- PubMed:
- 28176794
- Factor de Impacto:
- 6,582 SCImago ℠
- Cuartil:
- Q1 SCImago ℠
Nature Communications NATURE PORTFOLIO
Citas Recibidas en Web of Science: 122
Documentos
- No hay documentos
Filiaciones
Keywords
- OF-FUNCTION MUTATIONS; IDENTIFIES MUTATIONS; R2TP COMPLEX; DEFECTS; OUTER; PROTEIN; ARMS; VARIANTS; MOTILITY; INNER
Campos de Estudio
Cita
Olcese C,Patel MP,Shoemark A,Kiviluoto S,Legendre M,Williams HJ,Vaughan CK,Hayward J,Goldenberg A,Emes RD,Munye MM,Dyer L,Cahill T,Bevillard J,Gehrig C,Guipponi M,Chantot S,Duquesnoy P,Thomas L,Jeanson L,Copin B,Tamalet A,Thauvin C,Papon J,Garin A,Pin I,Vera G,Aurora P,Fassad MR,Jenkins L,Boustred C,Cullup T,Dixon M,Onoufriadis A,Bush A,Chung EMK,Antonarakis SE,Loebinger MR,Wilson R,ARMENGOT M,Escudier E,Hogg C,Amselem S,Sun Z,Bartoloni L,Blouin J,Mitchison HM,UK10K GRP. X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3. Nat. Commun. 2017. 8. 14279. IF:12,353. (1).