Identification of a novel CFAP61 homozygous splicing variant associated with multiple morphological abnormalities of the flagella.

CFAP61 Exome sequencing Genetics of male infertility MMAF

Journal

Journal of assisted reproduction and genetics
ISSN: 1573-7330
Titre abrégé: J Assist Reprod Genet
Pays: Netherlands
ID NLM: 9206495

Informations de publication

Date de publication:
22 May 2024
Historique:
received: 25 01 2024
accepted: 07 05 2024
medline: 22 5 2024
pubmed: 22 5 2024
entrez: 22 5 2024
Statut: aheadofprint

Résumé

In this study, we investigated the role of a newly identified homozygous variant (c.1245 + 6T > C) in the CFAP61 gene in the development of multiple morphologically abnormal flagella (MMAF) in an infertile patient. Using exome sequencing, we identified this variant, which led to exon 12 skipping and the production of a truncated CFAP61 protein. Transmission electron microscopy analysis of the patient's spermatozoa revealed various flagellar abnormalities, including defective nuclear chromatin condensation, axoneme disorganization, and mitochondria embedded in residual cytoplasmic droplets. Despite a fertilization rate of 83.3% through ICSI, there was no successful pregnancy due to poor embryo quality.Our findings suggest a link between the identified CFAP61 variant and MMAF, indicating potential disruption in radial spokes' assembly or function crucial for normal ciliary motility. Furthermore, nearly half of the observed sperm heads displayed chromatin condensation defects, possibly contributing to the low blastulation rate. This case underscores the significance of genetic counseling and testing, particularly for couples dealing with infertility and MMAF. Early identification of such genetic variants can guide appropriate interventions and improve reproductive outcomes.

Identifiants

pubmed: 38775994
doi: 10.1007/s10815-024-03139-0
pii: 10.1007/s10815-024-03139-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Anne-Laure Barbotin (AL)

UMRS1172 Development and Plasticity of the Neuroendocrine Brain, University of Lille, Lille, France.
Institut de Biologie de la Reproduction-Spermiologie-CECOS, CHU Lille, Lille, France.

Angèle Boursier (A)

UMRS1172 Development and Plasticity of the Neuroendocrine Brain, University of Lille, Lille, France.
Institut de Biologie de la Reproduction-Spermiologie-CECOS, CHU Lille, Lille, France.

Anne-Sophie Jourdain (AS)

ULR7364 -RADEME - Maladies Rares du Développement Embryonnaire, University of Lille, Lille, France.
Institut de Génétique Médicale, CHU Lille, Avenue Oscar Lambret, F-59000, Lille, France.

Alexandre Moerman (A)

Clinique de Génétique Guy Fontaine, CHU Lille, Lille, France.

Baptiste Rabat (B)

ULR7364 -RADEME - Maladies Rares du Développement Embryonnaire, University of Lille, Lille, France.

Mariam Chehimi (M)

Institut de Biologie de la Reproduction-Spermiologie-CECOS, CHU Lille, Lille, France.

Caroline Thuillier (C)

Institut de Génétique Médicale, CHU Lille, Avenue Oscar Lambret, F-59000, Lille, France.

Jamal Ghoumid (J)

ULR7364 -RADEME - Maladies Rares du Développement Embryonnaire, University of Lille, Lille, France.
Clinique de Génétique Guy Fontaine, CHU Lille, Lille, France.

Thomas Smol (T)

ULR7364 -RADEME - Maladies Rares du Développement Embryonnaire, University of Lille, Lille, France. thomas.smol@chu-lille.fr.
Institut de Génétique Médicale, CHU Lille, Avenue Oscar Lambret, F-59000, Lille, France. thomas.smol@chu-lille.fr.

Classifications MeSH