4.5 Article

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice

期刊

JOURNAL OF MEDICAL GENETICS
卷 59, 期 7, 页码 710-718

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/jmedgenet-2021-107919

关键词

genetics; medical; genetic variation; reproductive medicine

资金

  1. National Natural Science Foundation of China [31625015, 31521003, 81971441, 32000393]
  2. Shanghai Municipal Science and Technology Major Project [2017SHZDZX01]
  3. Anhui Medical University [TP202002]
  4. Innovative Research Team of High-level Local Universities in Shanghai [SSMU-ZLCX20180500]
  5. Science and Technology Major Project of Inner Mongolia Autonomous Region of China [zdzx2018065]
  6. 111 Project [B13016]
  7. State Key Laboratory of Reproductive Medicine [SKLRM-K202002]
  8. Scientific Research Project of Jiangsu Provincial Health and Family Planning Commission [H2018050]
  9. Maternal and Child Health Research Project of Jiangsu Province [F201866]
  10. French Research Agency (ANR) project FLAGEL-OME [ANR-19-CE17-0014]

向作者/读者索取更多资源

This study identified CCDC34 gene as a key player in III male asthenozoospermia, and through genetic analysis and cell experiments on the samples, revealed the importance of the CCDC34 gene in sperm flagella morphology.
Background Oligoasthenoteratozoospermia is a typical feature of sperm malformations leading to male infertility. Only a few genes have been clearly identified as pathogenic genes of oligoasthenoteratozoospermia. Methods and results Here, we identified a homozygous frameshift variant (c.731dup, p.Asn244Lysfs*3) in CCDC34, which is preferentially expressed in the human testis, using whole-exome sequencing in a cohort of 100 Chinese men with multiple morphological abnormalities of the sperm flagella (MMAF). In an additional cohort of 167 MMAF-affected men from North Africa, Iran and France, we identified a second subject harbouring a homozygous CCDC34 frameshift variant (c.799_817del, p.Glu267Lysfs*72). Both affected men presented a typical MMAF phenotype with an abnormally low sperm concentration (ie, oligoasthenoteratozoospermia). Transmission electron microscopy analysis of the sperm flagella affected by CCDC34 deficiency further revealed dramatic disorganisation of the axoneme. Immunofluorescence assays of the spermatozoa showed that CCDC34 deficiency resulted in almost absent staining of CCDC34 and intraflagellar transport-B complex-associated proteins (such as IFT20 and IFT52). Furthermore, we generated a mouse Ccdc34 frameshift mutant using CRISPR-Cas9 technology. Ccdc34-mutated (Ccdc34(mut/mut) ) male mice were sterile and presented oligoasthenoteratozoospermia with typical MMAF anomalies. Intracytoplasmic sperm injection has good pregnancy outcomes in both humans and mice. Conclusions Our findings support that CCDC34 is crucial to the formation of sperm flagella and that biallelic deleterious mutations in CCDC34/Ccdc34 cause male infertility with oligoasthenoteratozoospermia in humans and mice.

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