Journal
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES
Volume 19, Issue 2, Pages 393-411Publisher
IVYSPRING INT PUBL
DOI: 10.7150/ijbs.76051
Keywords
Infertility; asthenoteratozoospermia; mitochondrial sheath; FSIP2; ICSI
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Compound heterozygous variants of FSIP2 were identified in three unrelated individuals with asthenoteratozoospermia, causing severe defects in fibrous sheath and axoneme. Additionally, other morphological abnormalities and successful pregnancies through ICSI were observed.
Asthenoteratozoospermia is one of the major factors for male infertility, whereas the causes of large numbers of cases are still unknown. We identified compound heterozygous variants of FSIP2 in three unrelated individuals from a cohort of 105 patients with asthenoteratozoospermia by exome sequencing. Deleterious FSIP2 variations caused severe disassembly of the fibrous sheath and axonemal defects. Intriguingly, spermatozoa in our study manifested super-length mitochondrial sheaths, increased levels of the mitochondrial sheath outer membrane protein TOMM20 and decreased mitochondrial ATP consumption. Dislocation or deletion of the annulus and reduction or dislocation of the annulus protein SEPT4 were also observed. While the lengthened mitochondrial sheaths were not presented in men harboring SEPT4 variants. Furthermore, female partners of two of three men achieved successful pregnancies following intracytoplasmic sperm injection (ICSI). Overall, we presume that FSIP2 may not only serve as a structural protein of the fibrous sheath but also as an intra-flagellar transporter involving in the axonemal assembly, mitochondrial selection and the termination of mitochondrial sheath extension during spermatogenesis, and ICSI is an effective treatment for individuals with FSIP2-associated asthenoteratozoospermia.
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