Isolation and cytogenetic characterization of zebrafish meiotic prophase I mutants
- Saito, K., Siegfried, K.R., Nüsslein-Volhard, C., and Sakai, N.
- Developmental Dynamics : an official publication of the American Association of Anatomists 240(7): 1779-92 (Journal)
- Registered Authors
- Nüsslein-Volhard, Christiane, Sakai, Noriyoshi, Siegfried, Kellee
- male infertility, meiotic mutant, zebrafish, testis, spermatogenesis
- MeSH Terms
- Infertility, Male/genetics
- Meiotic Prophase I/genetics*
- 21594953 Full text @ Dev. Dyn.
Saito, K., Siegfried, K.R., Nüsslein-Volhard, C., and Sakai, N. (2011) Isolation and cytogenetic characterization of zebrafish meiotic prophase I mutants. Developmental Dynamics : an official publication of the American Association of Anatomists. 240(7):1779-92.
We describe here the isolation and cytogenetic characterization of three meiotic prophase I mutants, denoted ietsugu (its), iesada (isa), and iemochi (imo), isolated by a novel N-ethyl-N-nitrosourea mutagenesis screen for adult zebrafish gonadogenesis. Histological examination and flow cytometry analysis of testes from these mutants showed that each contained neither spermatids nor sperm. Staining for Sycp3 and cleaved Caspase-3 and TUNEL (terminal deoxynucleotidyl transferase–mediated deoxyuridinetriphosphate nick end-labeling) assay further revealed that its had defects at the onset of meiosis, and that isa and imo spermatocytes failed to progress past the zygotene stage with apoptosis occurring in the testicular somatic cells. Staining for phosphorylated histone H2AX showed that foci formation in leptotene spermatocytes was disrupted in isa and imo. Furthermore, in vitro differentiation experiments revealed the possibility that the defects and sterility associated with mutations were germ line autonomous. Our results thus indicate that each responsible gene is necessary for meiotic progression during spermatogenesis and for male fertility.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes