CDC14A phosphatase is essential for hearing and male fertility in mouse and human.

Journal: Human molecular genetics

Volume: 27

Issue: 5

Year of Publication: 2019

Affiliated Institutions:  Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD , USA. Section on Sensory Cell Development and Function, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD , USA. Laboratory of Molecular and Cellular Neurobiology, Section on Molecular and Cellular Signaling, National Institute of Mental Health, NIH, Bethesda, MD , USA. School of Biological Sciences, University of the Punjab, Lahore , Pakistan. Laboratoire Procédés de Criblage Moléculaire et Cellulaire, Centre de Biotechnologie de Sfax, Université de Sfax, Sfax , Tunisia. Center of Excellence in Molecular Biology, University of the Punjab, Lahore , Pakistan. Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology - Head and Neck Surgery, University of Iowa, Iowa City, , IA, USA. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran , Iran. Mouse Auditory Testing Core Facility, NIH, Bethesda, MD , USA. Auditory Development and Restoration Program, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD , USA. Division of Veterinary Resources, National Institutes of Health, Bethesda, MD , USA. Genetic Engineering Core, National Eye Institute, NIH, Bethesda, MD , USA. Genomics and Computational Biology Core, National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, MD , USA.

Abstract summary 

The Cell Division-Cycle-14 gene encodes a dual-specificity phosphatase necessary in yeast for exit from mitosis. Numerous disparate roles of vertebrate Cell Division-Cycle-14 (CDC14A) have been proposed largely based on studies of cultured cancer cells in vitro. The in vivo functions of vertebrate CDC14A are largely unknown. We generated and analyzed mutations of zebrafish and mouse CDC14A, developed a computational structural model of human CDC14A protein and report four novel truncating and three missense alleles of CDC14A in human families segregating progressive, moderate-to-profound deafness. In five of these families segregating pathogenic variants of CDC14A, deaf males are infertile, while deaf females are fertile. Several recessive mutations of mouse Cdc14a, including a CRISPR/Cas9-edited phosphatase-dead p.C278S substitution, result in substantial perinatal lethality, but survivors recapitulate the human phenotype of deafness and male infertility. CDC14A protein localizes to inner ear hair cell kinocilia, basal bodies and sound-transducing stereocilia. Auditory hair cells of postnatal Cdc14a mutants develop normally, but subsequently degenerate causing deafness. Kinocilia of germ-line mutants of mouse and zebrafish have normal lengths, which does not recapitulate the published cdc14aa knockdown morphant phenotype of short kinocilia. In mutant male mice, degeneration of seminiferous tubules and spermiation defects result in low sperm count, and abnormal sperm motility and morphology. These findings for the first time define a new monogenic syndrome of deafness and male infertility revealing an absolute requirement in vivo of vertebrate CDC14A phosphatase activity for hearing and male fertility.

Authors & Co-authors:  Imtiaz Ayesha A Belyantseva Inna A IA Beirl Alisha J AJ Fenollar-Ferrer Cristina C Bashir Rasheeda R Bukhari Ihtisham I Bouzid Amal A Shaukat Uzma U Azaiez Hela H Booth Kevin T KT Kahrizi Kimia K Najmabadi Hossein H Maqsood Azra A Wilson Elizabeth A EA Fitzgerald Tracy S TS Tlili Abdelaziz A Olszewski Rafal R Lund Merete M Chaudhry Taimur T Rehman Atteeq U AU Starost Matthew F MF Waryah Ali M AM Hoa Michael M Dong Lijin L Morell Robert J RJ Smith Richard J H RJH Riazuddin Sheikh S Masmoudi Saber S Kindt Katie S KS Naz Sadaf S Friedman Thomas B TB

Study Outcome 

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Citations :  Wood J.S., Hartwell L.H. (1982) A dependent pathway of gene functions leading to chromosome segregation in Saccharomyces cerevisiae. J. Cell. Biol., 94, 718–726.
Authors :  31
Identifiers
Doi : 10.1093/hmg/ddx440
SSN : 1460-2083
Study Population
Male,Males,Females
Mesh Terms
Animals
Other Terms
Study Design
Cross Sectional Study
Study Approach
Country of Study
Publication Country
England