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Deficiency of TBL1XR1 causes asthenozoospermia
- Source :
- Andrologia. 53
- Publication Year :
- 2021
- Publisher :
- Hindawi Limited, 2021.
-
Abstract
- Transducin (β)-like 1 X-linked receptor 1 (TBL1XR1) is an evolutionarily conserved protein related to spermatozoa. To clarify its role and mechanism of action in spermatozoa, qRT-PCR was used to analyse the expression of TBL1XR1 in human spermatozoa and mouse testes. The mice were established as an animal model by injecting the mice testes with small interfering RNA against TBL1XR1 or control siRNA. Our results indicated that deficiency of TBL1XR1 in mice reduced the motility of spermatozoa and disrupted the histone-to-protamine transition. We also found the decreased expression of TBL1XR1 in the spermatozoa of human patients with asthenozoospermia (AZ) compared with that in the spermatozoa of healthy males. Moreover, we carried out chromatin immunoprecipitation analyses and found that genes downstream of TBL1XR1 were related to sperm motility. Thus, TBL1XR1 might be related to sperm motility and might function through its downstream genes. Our data highlight the role of TBL1XR1 involved in spermatozoa and provide new molecular insights into the intricate systems required for male fertility.
- Subjects :
- Male
endocrine system
Small interfering RNA
Urology
030232 urology & nephrology
Receptors, Cytoplasmic and Nuclear
Motility
Biology
Asthenozoospermia
Mice
03 medical and health sciences
0302 clinical medicine
Endocrinology
medicine
Animals
Humans
Receptor
Gene
reproductive and urinary physiology
Sperm motility
030219 obstetrics & reproductive medicine
urogenital system
Nuclear Proteins
General Medicine
medicine.disease
Spermatozoa
Cell biology
Repressor Proteins
Mechanism of action
Sperm Motility
medicine.symptom
Chromatin immunoprecipitation
Subjects
Details
- ISSN :
- 14390272 and 03034569
- Volume :
- 53
- Database :
- OpenAIRE
- Journal :
- Andrologia
- Accession number :
- edsair.doi.dedup.....63d842e993d9ef76b7a33985b4d4fa53
- Full Text :
- https://doi.org/10.1111/and.13980