Novel mutations of PMFBP1 in a man with acephalic spermatozoa defects. Issue 9 (20th July 2022)

• Record Type: Journal Article
• Authors: Nie, Hua; Tang, Yunge; Zhang, Xiaoyu; Tan, Yuqiu; Qin, Weibing
• Is Part Of: Molecular genetics & genomic medicine. Volume 10:Issue 9(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-07-20
• Subjects: acephalic spermatozoa -- headless sperm -- PMFBP1 gene -- truncated protein; Medical genetics -- Periodicals; Genomics -- Periodicals; 616.042
• DOI: 10.1002/mgg3.2020
• Languages: English
• ISSNs: 2324-9269

Abstract

Abstract: Background: Acephalic spermatozoa (AS) is a serious but rare reproductive genetic disorder that causes infertility in men. To date, only a few genes associated with AS defects have been identified, including the polyamine modulated factor 1 binding protein 1 ( PMFBP1 ) gene. Consistent with this, PMFBP1 localizes to the head–neck connection, which bridges the implantation fossa and basal body. Methods: A male patient was diagnosed as having an AS defect. Blood samples from all family members and a sample of the patient's semen were collected to determine the genetic causes of his infertility. Results: Compound heterozygote mutation in the PMFBP1 gene, which is associated with AS defects in the present case: two loss‐of‐function mutations, with one a nonsense mutation c.361C > T p.Gln121Ter, and another a splice donor mutation c.414 + 1G > T. The current study, together with previous studies, suggests that the nonsense mutation is responsible for a truncated PMFBP1 protein during its formation; a splice donor mutation c.414 + 1G > T might lead to new open reading frames, from which the dysfunction of an abnormal PMFBP1 protein might be predicted. Additionally, the expression of outer dense fiber 1 (ODF1) and ODF2 proteins has been experimentally shown to be regulated by the truncated PMFBP1 protein. Conclusion: We herein present a case with AS defects associated with heterozygote mutations of PMFBP1, which have been shown to be rare and pathogenic; the association with an AS defect is a monogenic disorder with a recessive inherited pattern in the patient's family. Abstract : Two novel heterozygote variations in the PMFBP1 gene, which are associated with acephalic spermatozoa defects, have been identified in the present case:one is a nonsense mutation, another is a splice donor mutation. The current study together with previous studies suggest that loss‐of‐function mutations are responsible for a truncated PMFBP1 protein during its formation. The mature PMFBP1 mRNA retains part of introns 4 and/or 5 forming an alternative structure of the PMFBP1 protein and changing the normal function of PMFBP1.