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. 1986 Nov 1;103(5):1855–1861. doi: 10.1083/jcb.103.5.1855

Identification of a 52-kD calmodulin-binding protein associated with the mitotic spindle apparatus in mammalian cells

PMCID: PMC2114387  PMID: 3536955

Abstract

A pool of 10 calmodulin-binding proteins (CBPs) was isolated from Chinese hamster ovary (CHO) cells via calmodulin (CaM)-Sepharose affinity chromatography. One of these ten isolated CBPs with a molecular mass of 52 kD was also found to be present in isolated CHO cell mitotic spindles. Affinity-purified antibodies generated against this pool of isolated CBPs recognize a single 52-kD protein in isolated CHO cell mitotic spindles by immunoblot analysis. Immunofluorescence examination of CHO, 3T3, NRK, PTK-2, and HeLa cells resulted in a distinct pattern of mitotic spindle fluorescence. The localization pattern of this 52-kD CBP directly parallels that of CaM in the spindle apparatus throughout the various stages of mitosis. Interestingly, there was no association of this 52-kD CBP with cytoplasmic microtubules. As is the case with CaM, the localization pattern of the 52-kD CBP in interphase cells is diffuse within the cytoplasm and is not associated with any discrete, cellular structures. This 52-kD CBP appears to represent the first mitotic spindle-specific calmodulin- binding protein identified and represents an initial step toward the ultimate determination of CaM function in the mitotic spindle apparatus.

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Selected References

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  1. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
  2. Brady R. C., Karnaky K. J., Jr, Dedman J. R. Reserpine-induced alterations in mucus production and calmodulin-binding proteins in a human epithelial cell line. Exp Cell Res. 1984 Jan;150(1):141–151. doi: 10.1016/0014-4827(84)90709-2. [DOI] [PubMed] [Google Scholar]
  3. Cabral F., Sobel M. E., Gottesman M. M. CHO mutants resistant to colchicine, colcemid or griseofulvin have an altered beta-tubulin. Cell. 1980 May;20(1):29–36. doi: 10.1016/0092-8674(80)90231-7. [DOI] [PubMed] [Google Scholar]
  4. Chafouleas J. G., Dedman J. R., Munjaal R. P., Means A. R. Calmodulin. Development and application of a sensitive radioimmunoassay. J Biol Chem. 1979 Oct 25;254(20):10262–10267. [PubMed] [Google Scholar]
  5. Davis B. A., Schwartz A., Samaha F. J., Kranias E. G. Regulation of cardiac sarcoplasmic reticulum calcium transport by calcium-calmodulin-dependent phosphorylation. J Biol Chem. 1983 Nov 25;258(22):13587–13591. [PubMed] [Google Scholar]
  6. Dean W. L., Sullivan D. M. Structural and functional properties of a Ca2+-ATPase from human platelets. J Biol Chem. 1982 Dec 10;257(23):14390–14394. [PubMed] [Google Scholar]
  7. Dedman J. R., Welsh M. J., Means A. R. Ca2+-dependent regulator. Production and characterization of a monospecific antibody. J Biol Chem. 1978 Oct 25;253(20):7515–7521. [PubMed] [Google Scholar]
  8. Famulski K. S., Carafoli E. Calmodulin-dependent protein phosphorylation and calcium uptake in rat-liver microsomes. Eur J Biochem. 1984 May 15;141(1):15–20. doi: 10.1111/j.1432-1033.1984.tb08149.x. [DOI] [PubMed] [Google Scholar]
  9. Gorelick F. S., Cohn J. A., Freedman S. D., Delahunt N. G., Gershoni J. M., Jamieson J. D. Calmodulin-stimulated protein kinase activity from rat pancreas. J Cell Biol. 1983 Oct;97(4):1294–1298. doi: 10.1083/jcb.97.4.1294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hawkes R., Niday E., Gordon J. A dot-immunobinding assay for monoclonal and other antibodies. Anal Biochem. 1982 Jan 1;119(1):142–147. doi: 10.1016/0003-2697(82)90677-7. [DOI] [PubMed] [Google Scholar]
  11. Izant J. G., Weatherbee J. A., McIntosh J. R. A microtubule-associated protein antigen unique to mitotic spindle microtubules in PtK1 cells. J Cell Biol. 1983 Feb;96(2):424–434. doi: 10.1083/jcb.96.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Izant J. G., Weatherbee J. A., McIntosh J. R. A microtubule-associated protein in the mitotic spindle and the interphase nucleus. Nature. 1982 Jan 21;295(5846):248–250. doi: 10.1038/295248a0. [DOI] [PubMed] [Google Scholar]
  13. Jameson L., Caplow M. Modification of microtubule steady-state dynamics by phosphorylation of the microtubule-associated proteins. Proc Natl Acad Sci U S A. 1981 Jun;78(6):3413–3417. doi: 10.1073/pnas.78.6.3413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Jameson L., Frey T., Zeeberg B., Dalldorf F., Caplow M. Inhibition of microtubule assembly by phosphorylation of microtubule-associated proteins. Biochemistry. 1980 May 27;19(11):2472–2479. doi: 10.1021/bi00552a027. [DOI] [PubMed] [Google Scholar]
  15. Kanagasuntheram P., Teo T. S. Calmodulin-sensitive ATP-dependent calcium transport by the rat parotid endoplasmic reticulum. FEBS Lett. 1982 May 17;141(2):233–236. doi: 10.1016/0014-5793(82)80055-0. [DOI] [PubMed] [Google Scholar]
  16. Keller T. C., 3rd, Jemiolo D. K., Burgess W. H., Rebhun L. I. Strongylocentrotus purpuratus spindle tubulin. II. Characteristics of its sensitivity to Ca++ and the effects of calmodulin isolated from bovine brain and S. purpuratus eggs. J Cell Biol. 1982 Jun;93(3):797–803. doi: 10.1083/jcb.93.3.797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kiehart D. P. Studies on the in vivo sensitivity of spindle microtubules to calcium ions and evidence for a vesicular calcium-sequestering system. J Cell Biol. 1981 Mar;88(3):604–617. doi: 10.1083/jcb.88.3.604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kirchberger M. A., Antonetz T. Calmodulin-mediated regulation of calcium transport and (Ca2+ + Mg2+)-activated ATPase activity in isolated cardiac sarcoplasmic reticulum. J Biol Chem. 1982 May 25;257(10):5685–5691. [PubMed] [Google Scholar]
  19. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  20. Lee Y. C., Wolff J. The calmodulin-binding domain on microtubule-associated protein 2. J Biol Chem. 1984 Jul 10;259(13):8041–8044. [PubMed] [Google Scholar]
  21. Marcum J. M., Dedman J. R., Brinkley B. R., Means A. R. Control of microtubule assembly-disassembly by calcium-dependent regulator protein. Proc Natl Acad Sci U S A. 1978 Aug;75(8):3771–3775. doi: 10.1073/pnas.75.8.3771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. McGuinness T. L., Lai Y., Greengard P. Ca2+/calmodulin-dependent protein kinase II. Isozymic forms from rat forebrain and cerebellum. J Biol Chem. 1985 Feb 10;260(3):1696–1704. [PubMed] [Google Scholar]
  23. Means A. R., Dedman J. R. Calmodulin--an intracellular calcium receptor. Nature. 1980 May 8;285(5760):73–77. doi: 10.1038/285073a0. [DOI] [PubMed] [Google Scholar]
  24. Mullins J. M., McIntosh J. R. Isolation and initial characterization of the mammalian midbody. J Cell Biol. 1982 Sep;94(3):654–661. doi: 10.1083/jcb.94.3.654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Palfrey H. C., Rothlein J. E., Greengard P. Calmodulin-dependent protein kinase and associated substrates in Torpedo electric organ. J Biol Chem. 1983 Aug 10;258(15):9496–9503. [PubMed] [Google Scholar]
  26. Petzelt C. Biochemistry of the mitotic spindle. Int Rev Cytol. 1979;60:53–92. doi: 10.1016/s0074-7696(08)61259-0. [DOI] [PubMed] [Google Scholar]
  27. Petzelt C. Localization of an intracellular membrane-bound Ca2+-ATPase in PtK-cells using immunofluorescence techniques. Eur J Cell Biol. 1984 Jan;33(1):55–59. [PubMed] [Google Scholar]
  28. Renart J., Reiser J., Stark G. R. Transfer of proteins from gels to diazobenzyloxymethyl-paper and detection with antisera: a method for studying antibody specificity and antigen structure. Proc Natl Acad Sci U S A. 1979 Jul;76(7):3116–3120. doi: 10.1073/pnas.76.7.3116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Salmon E. D., Segall R. R. Calcium-labile mitotic spindles isolated from sea urchin eggs (Lytechinus variegatus). J Cell Biol. 1980 Aug;86(2):355–365. doi: 10.1083/jcb.86.2.355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Schulman H. Differential phosphorylation of MAP-2 stimulated by calcium-calmodulin and cyclic AMP. Mol Cell Biol. 1984 Jun;4(6):1175–1178. doi: 10.1128/mcb.4.6.1175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Silver R. B., Cole R. D., Cande W. Z. Isolation of mitotic apparatus containing vesicles with calcium sequestration activity. Cell. 1980 Feb;19(2):505–516. doi: 10.1016/0092-8674(80)90525-5. [DOI] [PubMed] [Google Scholar]
  32. Sobue K., Fujita M., Muramoto Y., Kakiuchi S. The calmodulin-binding protein in microtubules is tau factor. FEBS Lett. 1981 Sep 14;132(1):137–140. doi: 10.1016/0014-5793(81)80447-4. [DOI] [PubMed] [Google Scholar]
  33. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Welsh M. J., Dedman J. R., Brinkley B. R., Means A. R. Calcium-dependent regulator protein: localization in mitotic apparatus of eukaryotic cells. Proc Natl Acad Sci U S A. 1978 Apr;75(4):1867–1871. doi: 10.1073/pnas.75.4.1867. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Welsh M. J., Dedman J. R., Brinkley B. R., Means A. R. Tubulin and calmodulin. Effects of microtubule and microfilament inhibitors on localization in the mitotic apparatus. J Cell Biol. 1979 Jun;81(3):624–634. doi: 10.1083/jcb.81.3.624. [DOI] [PMC free article] [PubMed] [Google Scholar]

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