Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice

• Published in: Human reproduction open 2024, Vol.2024 (1), p.hoae003
• Main Authors: Meng, Gui-Quan, Wang, Yaling, Luo, Chen, Tan, Yu-Mei, Li, Yong, Tan, Chen, Tu, Chaofeng, Zhang, Qian-Jun, Hu, Liang, Zhang, Huan, Meng, Lan-Lan, Liu, Chun-Yu, Deng, Leiyu, Lu, Guang-Xiu, Lin, Ge, Du, Juan, Tan, Yue-Qiu, Sha, Yanwei, Wang, Lingbo, He, Wen-Bin
• Format: Article
• Language: English
• Subjects: Causes of; Dynein; Genetic aspects; Genetic variation; Health aspects; Infertility, Male; Medical research; Medicine, Experimental
• ISSN: 2399-3529; 2399-3529
• DOI: 10.1093/hropen/hoae003

STUDY QUESTION Are there other pathogenic genes for asthenoteratozoospermia (AT)? SUMMARY ANSWER DNAH3 is a novel candidate gene for AT in humans and mice. WHAT IS KNOWN ALREADY AT is a major cause of male infertility. Several genes underlying AT have been reported; however, the genetic aetiology remains unknown in a majority of affected men. STUDY DESIGN, SIZE, DURATION A total of 432 patients with AT were recruited in this study. DNAH3 mutations were identified by whole-exome sequencing (WES). Dnah3 knockout mice were generated using the genome editing tool. The morphology and motility of sperm from Dnah3 knockout mice were investigated. The entire study was conducted over 3 years. PARTICIPANTS/MATERIALS, SETTING, METHODS WES was performed on 432 infertile patients with AT. In addition, two lines of Dnah3 knockout mice were generated. Haematoxylin and eosin (H&E) staining, transmission electron microscopy (TEM), immunostaining, and computer-aided sperm analysis (CASA) were performed to investigate the morphology and motility of the spermatozoa. ICSI was used to overcome the infertility of one patient and of the Dnah3 knockout mice. MAIN RESULTS AND THE ROLE OF CHANCE DNAH3 biallelic variants were identified in three patients from three unrelated families. H&E staining revealed various morphological abnormalities in the flagella of sperm from the patients, and TEM and immunostaining further showed the loss of the central pair of microtubules, a dislocated mitochondrial sheath and fibrous sheath, as well as a partial absence of the inner dynein arms. In addition, the two Dnah3 knockout mouse lines demonstrated AT. One patient and the Dnah3 knockout mice showed good treatment outcomes after ICSI. LARGE SCALE DATA N/A. LIMITATIONS, REASONS FOR CAUTION This is a preliminary report suggesting that defects in DNAH3 can lead to asthenoteratozoospermia in humans and mice. The pathogenic mechanism needs to be further examined in a future study. WIDER IMPLICATIONS OF THE FINDINGS Our findings show that DNAH3 is a novel candidate gene for AT in humans and mice and provide crucial insights into the biological underpinnings of this disorder. The findings may also be beneficial for counselling affected individuals. STUDY FUNDING/COMPETING INTEREST(S) This work was supported by grants from National Natural Science Foundation of China (82201773, 82101961, 82171608, 32322017, 82071697, and 81971447), National Key Research and Development Program of China (2022YFC2702604),