Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility

dc.contributor.authorGerlevik, Umut
dc.contributor.authorErgoren, Mahmut Cerkez
dc.contributor.authorSezerman, Osman Ugur
dc.contributor.authorTemel, Sehime Gulsun
dc.date.accessioned2023-02-21T12:37:08Z
dc.date.available2023-02-21T12:37:08Z
dc.date.issued2022-01-01
dc.description.abstractBackground: Impaired meiosis can result in absence of sperm in the seminal fluid. This condition, namely non-obstructive azoospermia (NOA), is one of the reasons of male infertility. Despite the low number of studies on meiosis 1-associated protein (M1AP) in the literature, MIAP is known to be crucial for spermatogenesis. Recently, seven variants (five missense, one frameshift, one splice-site) have been reported in the MIAP gene as associated with NOA, cryptozoospermia and oligozoospermia in two separate studies. However, all missense variants were evaluated as variant of uncertain significance by these studies. Therefore, we aimed to analyze their structural impacts on the M1AP protein that could lead to NOA. Methods: We firstly performed an evolutionary conservation analysis for the variant positions. Afterwards, a comprehensive molecular modelling study was performed for the M1AP structure. By utilizing this model, protein dynamics were sampled for the wild-type and variants by performing molecular dynamics (MD) simulations. Results: All variant positions are highly conserved, indicating that they are potentially important for function. In MD simulations, none of the variants led to a general misfolding or loss of stability in the protein structure, but they did cause severe modifications in the conformational dynamics of M1AP, particularly through changes in local interactions affecting flexibility, hinge and secondary structure. Conclusions: Due to critical perturbations in protein dynamics, we propose that these variants may cause NOA by affecting important interactions regulating meiosis, particularly in wild-type M1AP deficiency since the variants are reported to be homozygous or bi-allelic in the infertile individuals. Our results provided reasonable insights about the MIAP structure and the effects of the variants to the structure and dynamics, which should be further investigated by experimental studies to validate.
dc.description.issueMAR 21
dc.description.volume10
dc.identifier.doi10.7717/peerj.12947
dc.identifier.urihttps://hdl.handle.net/11443/2203
dc.identifier.urihttp://dx.doi.org/10.7717/peerj.12947
dc.identifier.wosWOS:000775102200001
dc.publisherPEERJ INC
dc.relation.ispartofPEERJ
dc.subjectMolecular modelling
dc.subjectMolecular dynamics simulations
dc.subjectMale infertility
dc.subjectMeisos 1-associated protein (M1AP)
dc.subjectNon-obstructive azoospermia (NOA)
dc.subjectCryptozoospermia
dc.subjectVariant effect on protein structure
dc.titleStructural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility
dc.typeArticle

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