Literature DB >> 23261303

Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia.

Alexandros Onoufriadis1, Tamara Paff, Dinu Antony, Amelia Shoemark, Dimitra Micha, Bertus Kuyt, Miriam Schmidts, Stavroula Petridi, Jeanette E Dankert-Roelse, Eric G Haarman, Johannes M A Daniels, Richard D Emes, Robert Wilson, Claire Hogg, Peter J Scambler, Eddie M K Chung, Gerard Pals, Hannah M Mitchison.   

Abstract

Defects in motile cilia and sperm flagella cause primary ciliary dyskinesia (PCD), characterized by chronic airway disease, infertility, and left-right laterality disturbances, usually as a result of loss of the outer dynein arms (ODAs) that power cilia/flagella beating. Here, we identify loss-of-function mutations in CCDC114 causing PCD with laterality malformations involving complex heart defects. CCDC114 is homologous to DCC2, an ODA microtubule-docking complex component of the biflagellate alga Chlamydomonas. We show that CCDC114 localizes along the entire length of human cilia and that its deficiency causes a complete absence of ciliary ODAs, resulting in immotile cilia. Thus, CCDC114 is an essential ciliary protein required for microtubular attachment of ODAs in the axoneme. Fertility is apparently not greatly affected by CCDC114 deficiency, and qPCR shows that this may explained by low transcript expression in testis compared to ciliated respiratory epithelium. One CCDC114 mutation, c.742G>A, dating back to at least the 1400s, presents an important diagnostic and therapeutic target in the isolated Dutch Volendam population.
Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23261303      PMCID: PMC3542455          DOI: 10.1016/j.ajhg.2012.11.002

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  48 in total

1.  Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates.

Authors:  D Jeganathan; R Chodhari; M Meeks; O Faeroe; D Smyth; K Nielsen; I Amirav; A S Luder; H Bisgaard; R M Gardiner; E M K Chung; H M Mitchison
Journal:  J Med Genet       Date:  2004-03       Impact factor: 6.318

2.  Aetiology in adult patients with bronchiectasis.

Authors:  A Shoemark; L Ozerovitch; R Wilson
Journal:  Respir Med       Date:  2007-01-12       Impact factor: 3.415

3.  Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1.

Authors:  Masha Mazor; Soliman Alkrinawi; Vered Chalifa-Caspi; Esther Manor; Val C Sheffield; Micha Aviram; Ruti Parvari
Journal:  Am J Hum Genet       Date:  2011-04-14       Impact factor: 11.025

4.  Cell biology: How cilia beat.

Authors:  T J Mitchison; H M Mitchison
Journal:  Nature       Date:  2010-01-21       Impact factor: 49.962

5.  Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.

Authors:  Heike Olbrich; Karsten Häffner; Andreas Kispert; Alexander Völkel; Andreas Volz; Gürsel Sasmaz; Richard Reinhardt; Steffen Hennig; Hans Lehrach; Nikolaus Konietzko; Maimoona Zariwala; Peadar G Noone; Michael Knowles; Hannah M Mitchison; Maggie Meeks; Eddie M K Chung; Friedhelm Hildebrandt; Ralf Sudbrak; Heymut Omran
Journal:  Nat Genet       Date:  2002-01-14       Impact factor: 38.330

6.  CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.

Authors:  Anne-Christine Merveille; Erica E Davis; Anita Becker-Heck; Marie Legendre; Israel Amirav; Géraldine Bataille; John Belmont; Nicole Beydon; Frédéric Billen; Annick Clément; Cécile Clercx; André Coste; Rachelle Crosbie; Jacques de Blic; Stephane Deleuze; Philippe Duquesnoy; Denise Escalier; Estelle Escudier; Manfred Fliegauf; Judith Horvath; Kent Hill; Mark Jorissen; Jocelyne Just; Andreas Kispert; Mark Lathrop; Niki Tomas Loges; June K Marthin; Yukihide Momozawa; Guy Montantin; Kim G Nielsen; Heike Olbrich; Jean-François Papon; Isabelle Rayet; Gilles Roger; Miriam Schmidts; Henrique Tenreiro; Jeffrey A Towbin; Diana Zelenika; Hanswalter Zentgraf; Michel Georges; Anne-Sophie Lequarré; Nicholas Katsanis; Heymut Omran; Serge Amselem
Journal:  Nat Genet       Date:  2010-12-05       Impact factor: 38.330

Review 7.  To beat or not to beat: roles of cilia in development and disease.

Authors:  Inés Ibañez-Tallon; Nathaniel Heintz; Heymut Omran
Journal:  Hum Mol Genet       Date:  2003-04-01       Impact factor: 6.150

8.  Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality.

Authors:  Kenjiro Kosaki; Kazushige Ikeda; Kei Miyakoshi; Mari Ueno; Rika Kosaki; Daisuke Takahashi; Mamoru Tanaka; Chikao Torikata; Yasunori Yoshimura; Takao Takahashi
Journal:  Am J Med Genet A       Date:  2004-09-01       Impact factor: 2.802

9.  Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia.

Authors:  Philippe Duquesnoy; Estelle Escudier; Laetitia Vincensini; Judy Freshour; Anne-Marie Bridoux; André Coste; Antoine Deschildre; Jacques de Blic; Marie Legendre; Guy Montantin; Henrique Tenreiro; Anne-Marie Vojtek; Céline Loussert; Annick Clément; Denise Escalier; Philippe Bastin; David R Mitchell; Serge Amselem
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

10.  Mutations at twelve independent loci result in absence of outer dynein arms in Chylamydomonas reinhardtii.

Authors:  R Kamiya
Journal:  J Cell Biol       Date:  1988-12       Impact factor: 10.539

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  69 in total

1.  Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.

Authors:  Esther Kott; Marie Legendre; Bruno Copin; Jean-François Papon; Florence Dastot-Le Moal; Guy Montantin; Philippe Duquesnoy; William Piterboth; Daniel Amram; Laurence Bassinet; Julie Beucher; Nicole Beydon; Eric Deneuville; Véronique Houdouin; Hubert Journel; Jocelyne Just; Nadia Nathan; Aline Tamalet; Nathalie Collot; Ludovic Jeanson; Morgane Le Gouez; Benoit Vallette; Anne-Marie Vojtek; Ralph Epaud; André Coste; Annick Clement; Bruno Housset; Bruno Louis; Estelle Escudier; Serge Amselem
Journal:  Am J Hum Genet       Date:  2013-08-29       Impact factor: 11.025

Review 2.  Cilia and coordination of signaling networks during heart development.

Authors:  Karen Koefoed; Iben Rønn Veland; Lotte Bang Pedersen; Lars Allan Larsen; Søren Tvorup Christensen
Journal:  Organogenesis       Date:  2013-12-17       Impact factor: 2.500

3.  ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry.

Authors:  Rim Hjeij; Anna Lindstrand; Richard Francis; Maimoona A Zariwala; Xiaoqin Liu; You Li; Rama Damerla; Gerard W Dougherty; Marouan Abouhamed; Heike Olbrich; Niki T Loges; Petra Pennekamp; Erica E Davis; Claudia M B Carvalho; Davut Pehlivan; Claudius Werner; Johanna Raidt; Gabriele Köhler; Karsten Häffner; Miguel Reyes-Mugica; James R Lupski; Margaret W Leigh; Margaret Rosenfeld; Lucy C Morgan; Michael R Knowles; Cecilia W Lo; Nicholas Katsanis; Heymut Omran
Journal:  Am J Hum Genet       Date:  2013-07-11       Impact factor: 11.025

Review 4.  Expanding horizons: ciliary proteins reach beyond cilia.

Authors:  Shiaulou Yuan; Zhaoxia Sun
Journal:  Annu Rev Genet       Date:  2013-09-06       Impact factor: 16.830

Review 5.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

Review 6.  Gene mutations in primary ciliary dyskinesia related to otitis media.

Authors:  Manuel Mata; Lara Milian; Miguel Armengot; Carmen Carda
Journal:  Curr Allergy Asthma Rep       Date:  2014-03       Impact factor: 4.806

7.  Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex.

Authors:  Heike Olbrich; Carolin Cremers; Niki T Loges; Claudius Werner; Kim G Nielsen; June K Marthin; Maria Philipsen; Julia Wallmeier; Petra Pennekamp; Tabea Menchen; Christine Edelbusch; Gerard W Dougherty; Oliver Schwartz; Holger Thiele; Janine Altmüller; Frank Rommelmann; Heymut Omran
Journal:  Am J Hum Genet       Date:  2015-09-17       Impact factor: 11.025

8.  Cilia Loss and Dynein Assembly Defects in Planaria Lacking an Outer Dynein Arm-Docking Complex Subunit.

Authors:  Ayaka Kyuji; Ramila S Patel-King; Toru Hisabori; Stephen M King; Ken-Ichi Wakabayashi
Journal:  Zoolog Sci       Date:  2020-02       Impact factor: 0.931

9.  Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms.

Authors:  Inga M Höben; Rim Hjeij; Heike Olbrich; Gerard W Dougherty; Tabea Nöthe-Menchen; Isabella Aprea; Diana Frank; Petra Pennekamp; Bernd Dworniczak; Julia Wallmeier; Johanna Raidt; Kim G Nielsen; Maria C Philipsen; Francesca Santamaria; Laura Venditto; Israel Amirav; Huda Mussaffi; Freerk Prenzel; Kaman Wu; Zeineb Bakey; Miriam Schmidts; Niki T Loges; Heymut Omran
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

10.  C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia.

Authors:  Mahmoud R Fassad; Amelia Shoemark; Pierrick le Borgne; France Koll; Mitali Patel; Mellisa Dixon; Jane Hayward; Charlotte Richardson; Emily Frost; Lucy Jenkins; Thomas Cullup; Eddie M K Chung; Michel Lemullois; Anne Aubusson-Fleury; Claire Hogg; David R Mitchell; Anne-Marie Tassin; Hannah M Mitchison
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

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