Detection of Mitotic Centromere-Associated Kinesin (MCAK) During Cell-Cycle Progression of Human Jurkat T Cells Using Polyclonal Antibody Raised Against Its N- Terminal Region Overexpressed in E. coli

  • Jun, Do-Youn (Laboratory of Immunobiology, Department of Microbiology, Kyungpook National University) ;
  • Rue, Seok-Woo (Laboratory of Immunobiology, Department of Microbiology, Kyungpook National University) ;
  • Kim, Byung-Woo (Laboratory of Immunobiology, Department of Microbiology, Kyungpook National University) ;
  • Kim, Young-Ho (Laboratory of Immunobiology, Department of Microbiology, Kyungpook National University)
  • Published : 2003.12.01

Abstract

Mitotic centromere-associated kinesin (MCAK), which is a novel kinesin with a central motor domain, is believed to playa role in mitotic segregation of chromosome during the M phase of the cell cycle. In the present study, it is shown that a rabbit polyclonal antibody has been produced using the N-terminal region (187 aa) of human MCAK expressed in E. coli as the antigen. To express the N-terminal region in E. coli, the MCAK cDNA fragment encoding N-terminal 187 aa was obtained by PCR and was then inserted into the pET 3d expression vector. Molecular mass of the N-terminal region overexpressed in the presence of IPTG was 23.2 kDa on SDS-PAGE, and the protein was insoluble and mainly localized in the inclusion body that could be easily purified from the other cellular proteins. The N-terminal region was purified by electro-elution from the gel after the inclusion body was resolved on the SDS-PAGE. The antiserum obtained after tertiary immunization with the purified protein specifically recognized HsMCAK when subjected to Western blot analysis, and showed a fluctuation of the protein level during the cell cycle of human Jurkat T cells. Synchronization of the cell-cycle progression required for recovery of cells at a specific stage of the cell cycle was performed by either hydroxyurea or nocadazole, and subsequent release from each blocking at 2, 4, and 7 h. Northern and Western analyses revealed that both mRNA and protein of HsMCAK reached a maximum level in the S phase and declined to a basal level in the G1 phase. These results indicate that a polyclonal antibody raised against the N-terminal region (187 aa) of HsMCAK, overexpressed in E. coli, specifically detects HsMCAK (81 kDa), and it can analyze the differential expression of HsMCAK protein during the cell cycle.

Keywords

References

  1. J. Biol. Chem. v.242 Hydroxyurea: Reversal of inhibition and use as a cell-synchronizing agent Adams,R.L;J.G.Lindsay
  2. J. Cell Biol. v.119 Kinesin family in murine central nervous system Aizawa,H.;Y.Sekine;R.Takemura;Z.Zhang;M.Nangaku;N.Hirokawa https://doi.org/10.1083/jcb.119.5.1287
  3. Nucleic Acids Res. v.24 The PROSITE database, its status in 1995 Bairoch,A.;P.Bucher;K.Hofmann https://doi.org/10.1093/nar/24.1.189
  4. Protein Prof. v.2 Moter proteins 1: Kinesing Bloom,G.S.;S.A.Endow
  5. Trends Cell Biol. v.5 Biochemical and functional diversity of microtubule motors in the nervous system Brady,S.T. https://doi.org/10.1016/S0962-8924(00)88980-1
  6. Cancer Res. v.36 The effects of methyl[5-(2-thienylcarbonyl)-1H-benzimidazol-2-yl]carbamate (R 17934; NSC238159), a new synthetic antitumoral drug interfering with microtubules, on mammalian cells cultured in vitro De Brabander, M. J.;R. M. Van de Veire;F.E.Aerts;M.Borgers;P.A.Janssen
  7. Trends Biochem. Sci. v.16 Determinants of motor polarity in the kinesin proteins Endow,S.A. https://doi.org/10.1016/0968-0004(91)90089-E
  8. Anal. biochem. v.137 A technique for radiolabeling DNA restriction endonuclease fragment of high specific activity Feinberg,A.P.;B.Volgelstein https://doi.org/10.1016/0003-2697(84)90381-6
  9. Biochem. Biophys. Acta v.1359 Cloning and expression of human mitotic centromere-associated kinesin gene Kim,I.G.;D.Y.Jun;U.Sohn;Y.H.Kim https://doi.org/10.1016/S0167-4889(97)00103-1
  10. J. Immunol. v.149 Expression of the murine homologue of the cell cycle control protein p34$^{cdc2}$ in T lymphocytes Kim,Y.H.;T.J.Proust;M.J.Buchnolz;F.J.Chrest;A.A.Nordin
  11. Biotechniques v.11 An efficient method to purify active eukaryotic proteins from the inclusion bodies in Escherichia coli Lin,K.H.;S.Y.Cheng
  12. J. Cell Biol. v.129 KIF2 is a new microtubule-based anterograde motor that stransports membranous organelles distinct from those carried by kinesin heavy chain or KIF3A/B Noda,Y.;S.Yoshitake;S.Kondo;M.Nangaku;N.Hirokawa https://doi.org/10.1083/jcb.129.1.157
  13. J. Micriobiol. Biotechnol. v.12 Apoptotic activity of insect pathogenic fungus Paecilmyces japonica towar human acute leukemia Jakat T cells is associated with mitochondria-dependent caspase-3 activation regulated by Bcl-2 Park,H.W.;D.Y.Jun;Y.H.Kim
  14. J. Microbiol. Biotechnol. v.10 Antitumor activity of Paecilomyces japonica is mediated by apoptotic cell death Park,Y.H.;E.K.Moon;Y.K.Shin;M.A.Bae;J.G.Kim;Y.H.Kim
  15. Trends Biochem. Sci. v.15 The P-loop, a common motif in ATP- and GTP-binding proteins Saraste,M.;P.R.Sibbald;A.Wittinghofer https://doi.org/10.1016/0968-0004(90)90281-F
  16. Science v.274 Cancer cell cycles Sherr,C.J. https://doi.org/10.1126/science.274.5293.1672
  17. Methods in Enzymology v.185 Use of T7 RNa polymerase to direct expression of cloned gene Studier,F.W.;A.H.Rosenberg;J.J.Dunn;J.W.Dobendorff;D.Goeddel(ed.) https://doi.org/10.1016/0076-6879(90)85008-C
  18. Annu. Rev. Biochem. v.59 Moter proteins of cytoplasmic microtubules Vallee,R.B.;H.S.Shpetner https://doi.org/10.1146/annurev.bi.59.070190.004401
  19. Curr. Opin. Cell Biol. v.8 Motors involved in spindle assembly and chromosome segregation Vernos,I.;E.Karsentik https://doi.org/10.1016/S0955-0674(96)80041-X
  20. Cell v.85 XKCMI: A Xenopus kinesin-related protein that regulates microtubule dynamics during mitosis spindle assembly Walczak,C.E.;T.J.Mitchison https://doi.org/10.1016/S0092-8674(00)81295-7
  21. Cell v.84 Kinesin-related proteins at mitotic spindle poles: Function and regulation Walczak,C.E.;T.J.Mitchison;A.Desai https://doi.org/10.1016/S0092-8674(00)80991-5
  22. EMBO J. v.1 Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP requiring enzymes and a common nucleotide binding fold Walker,J.E.;M.Saraste;M.J.Runswick;N.J.Gay
  23. J. Cell Biol. v.133 DSK1, a novel kinesin-related protein from the diatom Cylindrotheca fusiformis that is involved in anaphase spindle elongation Wein,H.;M.Foss;B.Brady;W.Z.Cande https://doi.org/10.1083/jcb.133.3.595
  24. J. Cell Biol. v.128 Identification and partial characterization of mitotic centromere-associated kinesin, a kinesin-related protein that associates with centromeres during mitosis Wordeman,L.;T.J.Mitchison https://doi.org/10.1083/jcb.128.1.95
  25. Cell Biol. Int. v.23 Mutations in the APT-binding domain affect the subcellular distribution of mitotic centromere-associated kinesin (MCAK) Wordeman,L.;M.Wagenbach;T.Maney https://doi.org/10.1006/cbir.1999.0359