4.7 Article

DDB1-and CUL4-associated factor 8 plays a critical role in spermatogenesis

Journal

FRONTIERS OF MEDICINE
Volume 15, Issue 2, Pages 302-312

Publisher

SPRINGER
DOI: 10.1007/s11684-021-0851-8

Keywords

Dcaf8; male infertility; spermatogenesis

Funding

  1. Key Program of Natural Science Foundation of China [8153006, 81870112, 81970134]
  2. Shanghai Science and Technology Development Funds [18ZR1423600]
  3. Shanghai Collaborative Innovation Program on Regenerative Medicine and Stem Cell Research [2019CXJQ01]
  4. Samuel Waxman Cancer Research Foundation
  5. Innovative Research Team of High-level Local Universities in Shanghai

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The study demonstrated that DCAF8 plays a critical role in spermatogenesis and is a key component of CRL4 in the reproductive system. Knockout of the Dcaf8 gene led to male infertility in mice, with decreased sperm motility and increased morphological abnormalities.
Cullin-RING E3 ubiquitin ligase (CRL)-4 is a member of the large CRL family in eukaryotes. It plays important roles in a wide range of cellular processes, organismal development, and physiological and pathological conditions. DDB1- and CUL4-associated factor 8 (DCAF8) is a WD40 repeat-containing protein, which serves as a substrate receptor for CRL4. The physiological role of DCAF8 is unknown. In this study, we constructed Dcaf8 knockout mice. Homozygous mice were viable with no noticeable abnormalities. However, the fertility of Dcaf8-deficient male mice was markedly impaired, consistent with the high expression of DCAF8 in adult mouse testis. Sperm movement characteristics, including progressive motility, path velocity, progressive velocity, and track speed, were significantly lower in Dcaf8 knockout mice than in wild-type (WT) mice. However, the total motility was similar between WT and Dcaf8 knockout sperm. More than 40% of spermatids in Dcaf8 knockout mice showed pronounced morphological abnormalities with typical bent head malformation. The acrosome and nucleus of Dcaf8 knockout sperm looked similar to those of WT sperm. In vitro tests showed that the fertilization rate of Dcaf8 knockout mice was significantly reduced. The results demonstrated that DCAF8 plays a critical role in spermatogenesis, and DCAF8 is a key component of CRL4 function in the reproductive system.

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