DOI QR코드

DOI QR Code

Centrobin/Nip2 Expression In Vivo Suggests Its Involvement in Cell Proliferation

  • Lee, Jungmin (Department of Biological Sciences, Seoul National University) ;
  • Kim, Sunmi (Department of Biological Sciences, Seoul National University) ;
  • Jeong, Yeontae (Department of Biological Sciences, Seoul National University) ;
  • Rhee, Kunsoo (Department of Biological Sciences, Seoul National University)
  • Received : 2009.03.25
  • Accepted : 2009.05.06
  • Published : 2009.07.31

Abstract

Centrobin/Nip2 was initially identified as a centrosome protein that is critical for centrosome duplication and spindle assembly. In the present study, we determined the expression and subcellular localization of centrobin in selected mouse tissues. Immunoblot analysis revealed that the centrobin-specific band of 100 kDa was detected in all tissues tested but most abundantly in the thymus, spleen and testis. In the testis, centrobin was localized at the centrosomes of spermatocytes and early round spermatids, but no specific signal was detected in late round spermatids and elongated spermatids. Our results also revealed that the centrosome duplication occurs at interphase of the second meiotic division of the mouse male germ cells. The centrobin protein was more abundant in the mitotically active ovarian follicular cells and thymic cortex cells than in non-proliferating corpus luteal cells and thymic medullary cells. The expression pattern of centrobin suggests that the biological functions of centrobin are related to cell proliferation. Consistent with the proposal, we observed reduction of the centrobin levels when NIH3T3 became quiescent in the serum-starved culture conditions. However, a residual amount of centrobin was also detected at the centrosomes of the resting cells, suggesting its role for maintaining integrity of the centrosome, especially of the daughter centriole in the cells.

Keywords

Acknowledgement

Supported by : Ministry of Health and Welfare

References

  1. Andersen, J.S., Wilkinson, C.J., Mayor, T., Mortensen, P., Nigg, E.A., and Mann, M. (2003). Proteomic characterization of the human centrosome by protein correlation profiling. Nature 426, 570-574 https://doi.org/10.1038/nature02166
  2. Bettencourt-Dias, M., and Carvalho-Santos, Z. (2008). Double life of centrioles: CP110 in the spotlight. Trends Cell Biol. 18, 8-11 https://doi.org/10.1016/j.tcb.2007.11.002
  3. Blagden, S.P., and Glover, D.M. (2003). Polar expeditions--provisioning the centrosome for mitosis. Nat. Cell Biol. 5, 505-511 https://doi.org/10.1038/ncb0603-505
  4. Bornens, M. (2002). Centrosome composition and microtubule anchoring mechanisms. Curr. Opin. Cell Biol. 14, 25-34 https://doi.org/10.1016/S0955-0674(01)00290-3
  5. Jackman, M., Lindon, C., Nigg, E.A., and Pines, J. (2003). Active cyclin B1-Cdk1 first appears on centrosomes in prophase. Nat. Cell Biol. 5, 143-148 https://doi.org/10.1038/ncb918
  6. Jeong, Y., Lee, J., Kim, K., Yoo, J.C., and Rhee, K. (2007). Characterization of NIP2/centrobin, a novel substrate of Nek2, and its potential role in microtubule stabilization. J. Cell Sci. 120, 2106-2016 https://doi.org/10.1242/jcs.03458
  7. Kramer, A., Mailand, N., Lukas, C., Syljuasen, R.G., Wilkinson, C.J., Nigg, E.A., Bartek, J., and Lukas, J. (2004). Centrosomeassociated Chk1 prevents premature activation of cyclin-B-Cdk1 kinase. Nat. Cell Biol. 6, 884-891 https://doi.org/10.1038/ncb1165
  8. Krioutchkova, M.M., and Onishchenko, G.E. (1999). Structural and functional characteristics of the centrosome in gametogenesis and early embryogenesis of animals. Int. Rev. Cytol. 185, 107-156 https://doi.org/10.1016/S0074-7696(08)60150-3
  9. Loncarek, J., and Khodjakov, A. (2009). Ab ovo or novo? Mechanisms of centriole duplication. Mol. Cells 27, 135-142 https://doi.org/10.1007/s10059-009-0017-z
  10. Manandhar, G., Schatten, H., and Sutovsky, P. (2005). Centrosome reduction during gametogenesis and its significance. Biol. Reprod. 72, 2-13 https://doi.org/10.1095/biolreprod.104.031245
  11. Nigg, E.A. (2007). Centrosome duplication: of rules and licenses. Trends Cell Biol. 17, 215-221 https://doi.org/10.1016/j.tcb.2007.03.003
  12. Piel, M., Meyer, P., Khodjakov, A., Rieder, C.L., and Bornens, M. (2000). The respective contributions of the mother and daughter centrioles to centrosome activity and behavior in vertebrate cells. J. Cell Biol. 149, 317-330 https://doi.org/10.1083/jcb.149.2.317
  13. Rhee, K., and Wolgemuth, D.J. (1997). The NIMA-related kinase 2, Nek2, is expressed in specific stages of the meiotic cell cycle and associates with meiotic chromosomes. Development 124, 2167-2177
  14. Saunders, P.T., Turner, J.M., Ruggiu, M., Taggart, M., Burgoyne, P.S., Elliott, D., and Cooke, H.J. (2003). Absence of mDazl produces a final block on germ cell development at meiosis. Reproduction 126, 589-597 https://doi.org/10.1530/rep.0.1260589
  15. Tsou, M.F., and Stearns, T. (2006). Mechanism limiting centrosome duplication to once per cell cycle. Nature 442, 947-951 https://doi.org/10.1038/nature04985
  16. Yamashita, S., and Okada, Y. (2005). Application of heat-induced antigen retrieval to aldehyde-fixed fresh frozen sections. J. Histochem. Cytochem. 53, 1421-1432
  17. Zou, C., Li, J., Bai, Y., Gunning, W.T., Wazer, D.E., Band, V., and Gao, Q. (2005). Centrobin: a novel daughter centriole-associated protein that is required for centriole duplication. J. Cell Biol. 171, 437-445 https://doi.org/10.1083/jcb.200506185

Cited by

  1. Microarray-Based Analysis of Cell-Cycle Gene Expression During Spermatogenesis in the Mouse1 vol.83, pp.4, 2009, https://doi.org/10.1095/biolreprod.110.084889
  2. Inhibition of centriole duplication by centrobin depletion leads to p38@?p53 mediated cell-cycle arrest vol.22, pp.5, 2009, https://doi.org/10.1016/j.cellsig.2010.01.009
  3. Centrobin/NIP2 Is a Microtubule Stabilizer Whose Activity Is Enhanced by PLK1 Phosphorylation during Mitosis vol.285, pp.33, 2010, https://doi.org/10.1074/jbc.m109.099127
  4. Nek2 and its substrate, centrobin/Nip2, are required for proper meiotic spindle formation of the mouse oocytes vol.19, pp.1, 2009, https://doi.org/10.1017/s0967199410000183
  5. Total cellular glycomics allows characterizing cells and streamlining the discovery process for cellular biomarkers vol.110, pp.6, 2009, https://doi.org/10.1073/pnas.1214233110