Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage.


Journal

Gene
ISSN: 1879-0038
Titre abrégé: Gene
Pays: Netherlands
ID NLM: 7706761

Informations de publication

Date de publication:
15 Dec 2023
Historique:
received: 18 07 2023
revised: 10 08 2023
accepted: 22 08 2023
medline: 25 9 2023
pubmed: 26 8 2023
entrez: 25 8 2023
Statut: ppublish

Résumé

Naturally occurring balanced, unbalanced, and complex chromosomal rearrangements have been reported to cause pathogenic genomic or genetic variants leading to infertility and recurrent miscarriage. Therefore, balanced chromosomal rearrangements were used as genomic signposts for identification of candidate genes or genomic loci associated with male infertility due to defects of spermatogenesis, or with recurrent miscarriage. In three male probands, structural chromosomal variants and copy number variants were identified at nucleotide resolution by long-insert genome sequencing approaches and Sanger sequencing. The pathogenic potential of these and affected candidate genes was assessed based on convergent genomic and genotype-phenotype correlation data. Identification of balanced chromosomal rearrangement breakpoints and interpretation in the context of their genomic background of structural and copy number variants led us to conclude that the infertility due to oligoasthenozoospermia and oligozoospermia is most likely associated with a position effect on YIPF5 and SPATC1L, respectively. In a third proband with intellectual disability and recurrent miscarriage, disruption of CAMK2B causing autosomal dominant, intellectual developmental disorder 54 and increased meiotic segregation during gametogenesis of a der(22) are responsible for the reported phenotype. Our data further support the existence of loci at 5q23 and 21q22.3 for these spermatogenesis defects and highlight the importance of the naturally occurring balanced chromosomal rearrangements for assessment of the pathogenic mechanisms. Furthermore, we show comorbidities due to the same balanced chromosomal rearrangement caused by different pathogenic mechanisms.

Identifiants

pubmed: 37625567
pii: S0378-1119(23)00578-4
doi: 10.1016/j.gene.2023.147737
pii:
doi:

Substances chimiques

Vesicular Transport Proteins 0
YIPF5 protein, human 0
SPATC1L protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

147737

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [Dezso David reports financial support was provided by Fundação para a Ciência e a Tecnologia.].

Auteurs

Dezső David (D)

Department of Human Genetics, National Institute of Health Doctor Ricardo Jorge, 1649-016 Lisbon, Portugal. Electronic address: dezso.david@insa.min-saude.pt.

Joana Fino (J)

Department of Human Genetics, National Institute of Health Doctor Ricardo Jorge, 1649-016 Lisbon, Portugal.

Renata Oliveira (R)

Medical Genetics Service, University Hospital Centre of São João, 4200-319 Porto, Portugal.

Sofia Dória (S)

Department of Pathology, Genetics Service, Faculty of Medicine, University of Porto, 4200-450 Porto, Portugal; I3S-Health Research and Innovation Institute, University of Porto, 4200-135 Porto, Portugal.

Cynthia C Morton (CC)

Department of Obstetrics and Gynecology and of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Manchester Centre for Audiology and Deafness (ManCAD), University of Manchester M13 9PL, UK.

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Classifications MeSH