The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans
Male
0301 basic medicine
570
610
male infertility
Article
576
Tacrolimus Binding Proteins
LINE-1
Mice
03 medical and health sciences
Gynaecology - Radboud University Medical Center
Semen
Testis
meiosis
Animals
Humans
genetics
RNA, Small Interfering
Spermatogenesis
11 Medical and Health Sciences
Infertility, Male
Azoospermia
Genetics & Heredity
Genetics of Male Infertility Initiative (GEMINI) consortium
Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience
ta1184
azoospermia
06 Biological Sciences
spermatogenesis
oligozoospermia
FKBP6
Long Interspersed Nucleotide Elements
round spermatid arrest
Urology - Radboud University Medical Center
piRNA-pathway
Radboudumc 0: Other Research RIHS: Radboud Institute for Health Sciences
Radboudumc 10: Reconstructive and regenerative medicine RIHS: Radboud Institute for Health Sciences
DOI:
10.1016/j.ajhg.2022.09.002
Publication Date:
2022-09-22T14:36:18Z
AUTHORS (27)
ABSTRACT
Infertility affects around 7% of the male population and can be due to severe spermatogenic failure (SPGF), resulting in no or very few sperm in the ejaculate. We initially identified a homozygous frameshift variant in FKBP6 in a man with extreme oligozoospermia. Subsequently, we screened a total of 2,699 men with SPGF and detected rare bi-allelic loss-of-function variants in FKBP6 in five additional persons. All six individuals had no or extremely few sperm in the ejaculate, which were not suitable for medically assisted reproduction. Evaluation of testicular tissue revealed an arrest at the stage of round spermatids. Lack of FKBP6 expression in the testis was confirmed by RT-qPCR and immunofluorescence staining. In mice, Fkbp6 is essential for spermatogenesis and has been described as being involved in piRNA biogenesis and formation of the synaptonemal complex (SC). We did not detect FKBP6 as part of the SC in normal human spermatocytes, but small RNA sequencing revealed that loss of FKBP6 severely impacted piRNA levels, supporting a role for FKBP6 in piRNA biogenesis in humans. In contrast to findings in piRNA-pathway mouse models, we did not detect an increase in LINE-1 expression in men with pathogenic FKBP6 variants. Based on our findings, FKBP6 reaches a "strong" level of evidence for being associated with male infertility according to the ClinGen criteria, making it directly applicable for clinical diagnostics. This will improve patient care by providing a causal diagnosis and will help to predict chances for successful surgical sperm retrieval.
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