Expression of Murine Asb-9 During Mouse Spermatogenesis

  • Lee, Man Ryul (Department of Anatomy and Cell Biology and Department of Biomedical Science, Hanyang University, College of Medicine) ;
  • Kim, Soo Kyoung (Department of Anatomy and Cell Biology and Department of Biomedical Science, Hanyang University, College of Medicine) ;
  • Kim, Jong Soo (Department of Anatomy and Cell Biology and Department of Biomedical Science, Hanyang University, College of Medicine) ;
  • Rhim, Si Youn (Department of surgery, Hanyang University, College of Medicine) ;
  • Kim, Kye-Seong (Department of Anatomy and Cell Biology and Department of Biomedical Science, Hanyang University, College of Medicine)
  • Received : 2008.07.07
  • Accepted : 2008.09.03
  • Published : 2008.12.31

Abstract

We previously showed that Asb-4 and Asb-17 is uniquely expressed in developing male germ cells. A recent report showed that Asb-9 is specifically expressed in the kidney and testes; however, detailed expression patterns in developing germ cells have not been shown. Northern blot analysis in various tissues demonstrated that mAsb-9 was strongly expressed in the testes. Expression analysis by RT-PCR and Northern blot in developing mouse testes indicates that mAsb-9 is expressed from the fourth week after birth to adulthood, with the highest expression in round spermatids. Expression sites were further localized by in situ hybridization in the testes. Pachytene spermatocytes and spermatids expressed mAsb-9 but spermatogonia and generated spermatozoa did not. This study reveals that mAsb-9 could be a specific marker of active spermatogenesis and would be useful for studies of male germ cell development.

Keywords

Acknowledgement

Supported by : Korea Science and Engineering Foundation

References

  1. Bellve, A.R., Millette, C.F., Bhatnagar, Y.M., and O'Brien, D.A. (1977). Dissociation of the mouse testis and characterization of isolated spermatogenic cells. J. Histochem. Cytochem. 25, 480- 494 https://doi.org/10.1177/25.7.893996
  2. Breeden, L., and Nasmyth, K. (1987). Similarity between cell-cycle genes of budding yeast and fission yeast and the Notch gene of Drosophila. Nature 329, 651-654 https://doi.org/10.1038/329651a0
  3. Debrincat, M.A., Zhang, J.G., Willson, T.A., Silke, J., Connolly, L.M., Simpson, R.J., Alexander, W.S., Nicola, N.A., Kile, B.T., and Hilton, D.J. (2007). Ankyrin repeat and suppressors of cytokine signaling box protein asb-9 targets creatine kinase B for degradation. J. Biol. Chem 282 4728-4737 https://doi.org/10.1074/jbc.M609164200
  4. Guo, J.H., Saiyin, H., Wei, Y.H., Chen, S., Chen, L., Bi, G., Ma, L.J., Zhou, G.J., Huang, C.Q., Yu, L., et al. (2004). Expression of testis specific ankyrin repeat and SOCS box-containing 17 gene. Arch. Androl. 50, 155-161 https://doi.org/10.1080/01485010490425485
  5. Kile, B.T., Metcalf, D., Mifsud, S., DiRago, L., Nicola, N.A., Hilton, D.J., and Alexander, W.S. (2001). Functional analysis of Asb-1 using genetic modification in mice. Mol. Cell. Biol. 21, 6189-6197 https://doi.org/10.1128/MCB.21.18.6189-6197.2001
  6. Kim, K.S., Kim, M.S., Kim, S.K., and Baek, K.H. (2004). Murine Asb-17 expression during mouse testis development and spermatogenesis. Zygote 12, 151-156 https://doi.org/10.1017/S0967199404002722
  7. Kim, S.K., Rhim, S.Y., Lee, M.R., Kim, J.S., Kim, H.J., Lee, D.R., and Kim, K.S. (2008). Stage-specific expression of ankyrin and SOCS box protein-4 (Asb-4) during spermatogenesis. Mol. Cells 25, 317-321
  8. Kohroki, J., Nishiyama, T., Nakamura, T., and Masuho, Y. (2005). ASB proteins interact with Cullin5 and Rbx2 to form E3 ubiquitin ligase complexes. FEBS Lett. 579, 6796-6802 https://doi.org/10.1016/j.febslet.2005.11.016
  9. Nicholson, S.E., Willson, T.A., Farley, A., Starr, R., Zhang, J.G., Baca, M., Alexander, W.S., Metcalf, D., Hilton, D.J., and Nicola, N.A. (1999). Mutational analyses of the SOCS proteins suggest a dual domain requirement but distinct mechanisms for inhibition of LIF and IL-6 signal transduction. EMBO J. 18, 375-385 https://doi.org/10.1093/emboj/18.2.375
  10. Park, C., Choi, W.S., Kwon, H., and Kwon, Y.K. (2001). Temporal and spatial expression of neurotrophins and their receptors during male germ cell development. Mol. Cells 12, 360-367
  11. Rhee, K., and Wolgemuth, D.J. (2002). Tcp10 promoter-directed expression of the Nek2 gene in mouse meiotic spermatocytes. Mol. Cells 13, 85-90
  12. Romrell, L.J., Bellve, A.R., and Fawcett, D.W. (1976). Separation of mouse spermatogenic cells by sedimentation velocity. A morphological characterization. Dev. Biol. 49, 119-131 https://doi.org/10.1016/0012-1606(76)90262-1
  13. Sedgwick, S.G., and Smerdon, S.J. (1999). The ankyrin repeat: a diversity of interactions on a common structural framework. Trends Biochem. Sci. 24, 311-316 https://doi.org/10.1016/S0968-0004(99)01426-7
  14. Serrano, M., Hannon, G.J., and Beach, D. (1993). A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature 366, 704-707 https://doi.org/10.1038/366704a0
  15. Wharton, K.A., Johansen, K.M., Xu, T., and Artavanis-Tsakonas, S. (1985). Nucleotide sequence from the neurogenic locus notch implies a gene product that shares homology with proteins containing EGF-like repeats. Cell 43, 567-581 https://doi.org/10.1016/0092-8674(85)90229-6
  16. Yoshimura, A., Ohkubo, T., Kiguchi, T., Jenkins, N.A., Gilbert, D.J., Copeland, N.G., Hara, T., and Miyajima, A. (1995). A novel cytokine- inducible gene CIS encodes an SH2-containing protein that binds to tyrosine-phosphorylated interleukin 3 and erythropoietin receptors. EMBO J. 14, 2816-2826
  17. Yoshimura, T., Miyazaki, T., Toyoda, S., Miyazaki, S., Tashiro, F., Yamato, E., and Miyazaki, J. (2007). Gene expression pattern of Cue110: a member of the uncharacterized UPF0224 gene family preferentially expressed in germ cells. Gene Expr. Patterns 8. 27-35 https://doi.org/10.1016/j.modgep.2007.08.003