4.7 Article

FAM71F1 binds to RAB2A and RAB2B and is essential for acrosome formation and male fertility in mice

期刊

DEVELOPMENT
卷 148, 期 21, 页码 -

出版社

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.199644

关键词

Acrosome; Spermatogenesis; Globozoospermia; Mouse

资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT)/Japan Society for the Promotion of Science (JSPS) KAKENHI grants [JP19J12450, JP17H04987, JP21K19569, JP19J21619, JP18K14612, JP20H03172, JP19H05750, JP21H04753, JP21H05033]
  2. Takeda Science Foundation
  3. Nakajima Foundation
  4. Japan Agency for Medical Research and Development (AMED) [JP21gm5010001]
  5. Eunice Kennedy Shriver National Institute of Child Health and Human Development [P01HD087157, R01HD088412]
  6. Bill and Melinda Gates Foundation [INV-001902]

向作者/读者索取更多资源

The acrosome is a cap-shaped organelle derived from the Golgi apparatus, located over the anterior of the sperm nucleus, and highly conserved throughout evolution. FAM71F1 plays a crucial role in male fertility by forming a complex with active RAB2A/B to suppress excessive vesicle trafficking during acrosome formation.
The acrosome is a cap-shaped, Golgi-derived membranous organelle that is located over the anterior of the sperm nucleus and highly conserved throughout evolution. Although morphological changes during acrosome biogenesis in spermatogenesis have been well described, the molecular mechanism underlying this process is still largely unknown. Family with sequence similarity 71, member F1 and F2 (FAM71F1 and FAM71F2) are testis-enriched proteins that contain a RAB2B-binding domain, a small GTPase involved in vesicle transport and membrane trafficking. Here, by generating mutant mice for each gene, we found that Fam71f1 is essential for male fertility. In Fam71f1-mutant mice, the acrosome was abnormally expanded at the round spermatid stage, likely because of enhanced vesicle trafficking. Mass spectrometry analysis after immunoprecipitation indicated that, in testes, FAM71F1 binds not only RAB2B, but also RAB2A. Further study suggested that FAM71F1 binds to the GTP-bound active form of RAB2A/B, but not the inactive form. These results indicate that a complex of FAM71F1 and active RAB2A/B suppresses excessive vesicle trafficking during acrosome formation.

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