Affiliation:
1. Research Institute for Microbial Diseases Osaka University Suita Osaka Japan
2. Graduate School of Pharmaceutical Sciences Osaka University Suita Osaka Japan
3. The Institute of Medical Science The University of Tokyo Minato‐ku Tokyo Japan
4. Center for Infectious Disease Education and Research Osaka University Suita Osaka Japan
Abstract
AbstractBackgroundTSN (translin), also called testis brain RNA‐binding protein, binds to TSNAX (translin‐associated factor X) and is suggested to play diverse roles, such as RNA metabolism and DNA damage response. TSNAXIP1 (Translin‐associated factor X‐interacting protein 1) was identified as a TSNAX‐interacting protein using a yeast two‐hybrid system, but its function in vivo was unknown.ObjectiveTo reveal the function of TSNAXIP1 in vivo in mice.Materials and methodsWe generated Tsnaxip1 knockout mice using the CRISPR/Cas9 system and analyzed their fertility and sperm motility. Further, we generated 1700010I14Rik knockout mice, because 1700010I14RIK is also predominantly expressed in testes and contains the same Pfam (protein families) domain as TSNAXIP1.ResultsReduced male fertility and impaired sperm motility with asymmetric flagellar waveforms were observed in not only Tsnaxip1 but also 1700010I14Rik knockout mice. Unlike Tsn knockout mice, no abnormalities were found in testicular sections of either Tsnaxip1 or 1700010I14Rik knockout mice. Furthermore, TSNAXIP1 was detected in the sperm tail and fractionated with axonemal proteins.Discussion and conclusionUnlike the TSN–TSNAX complex, whose disruption causes abnormal vacuoles in mouse testes, TSNAXIP1 and 1700010I14RIK may play roles in regulating sperm flagellar beating patterns.
Funder
Takeda Science Foundation
Eunice Kennedy Shriver National Institute of Child Health and Human Development
Subject
Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism