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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1981 Aug;78(8):5000–5004. doi: 10.1073/pnas.78.8.5000

Periodic synthesis of microtubular proteins in the cell cycle of Physarum.

T G Laffler, M T Chang, W F Dove
PMCID: PMC320319  PMID: 6946448

Abstract

Periodic polypeptide labeling over the naturally synchronous nuclear replication cycle of Physarum polycephalum was analyzed by fluorography of two-dimensional electropherograms. Two sets of polypeptides, denoted as P and Q, showed strong periodicity; they were maximally labeled just prior to mitosis. This periodicity was shown to reflect synthesis rather than turnover or recovery. Both P and Q copolymerized with porcine microtubular proteins and displayed electrophoretic properties similar to those of porcine tubulins. The significance of the periodic synthesis of these microtubular proteins is discussed as a possible component within the chain of events that establishes the high mitotic synchrony of Physarum syncytia.

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Selected References

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  1. Ben-Ze'ev A., Farmer S. R., Penman S. Mechanisms of regulating tubulin synthesis in cultured mammalian cells. Cell. 1979 Jun;17(2):319–325. doi: 10.1016/0092-8674(79)90157-0. [DOI] [PubMed] [Google Scholar]
  2. Borisy G. G., Marcum J. M., Olmsted J. B., Murphy D. B., Johnson K. A. Purification of tubulin and associated high molecular weight proteins from porcine brain and characterization of microtubule assembly in vitro. Ann N Y Acad Sci. 1975 Jun 30;253:107–132. doi: 10.1111/j.1749-6632.1975.tb19196.x. [DOI] [PubMed] [Google Scholar]
  3. Bravo R., Celis J. E. A search for differential polypeptide synthesis throughout the cell cycle of HeLa cells. J Cell Biol. 1980 Mar;84(3):795–802. doi: 10.1083/jcb.84.3.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cohen W. D., Rebhun L. I. An estimate of the amount of microtubule protein in the isolated mitotic apparatus. J Cell Sci. 1970 Jan;6(1):159–176. doi: 10.1242/jcs.6.1.159. [DOI] [PubMed] [Google Scholar]
  5. Cooke D. J., Dee J. Plasmodium formation without change in nuclear DNA content in Physarum polycephalum. Genet Res. 1974 Jun;23(3):307–317. doi: 10.1017/s0016672300014944. [DOI] [PubMed] [Google Scholar]
  6. DANIEL J. W., BABCOCK K. L., SIEVERT A. H., RUSCH H. P. ORGANIC REQUIREMENTS AND SYNTHETIC MEDIA FOR GROWTH OF THE MYXOMYCETE PHYSARUM POLYCEPHALUM. J Bacteriol. 1963 Aug;86:324–331. doi: 10.1128/jb.86.2.324-331.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Elliott S. G., McLaughlin C. S. Rate of macromolecular synthesis through the cell cycle of the yeast Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4384–4388. doi: 10.1073/pnas.75.9.4384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gudas L. J., James R., Paradee A. B. Evidence of the involvement of an outer membrane protein in DNA initiation. J Biol Chem. 1976 Jun 10;251(11):3470–3479. [PubMed] [Google Scholar]
  9. Jäckle H. Visualization of proteins after isoelectric focusing during two-dimensional gel electrophoresis. Anal Biochem. 1979 Sep 15;98(1):81–84. doi: 10.1016/0003-2697(79)90708-5. [DOI] [PubMed] [Google Scholar]
  10. Lowe P. A., Hager D. A., Burgess R. R. Purification and properties of the sigma subunit of Escherichia coli DNA-dependent RNA polymerase. Biochemistry. 1979 Apr 3;18(7):1344–1352. doi: 10.1021/bi00574a034. [DOI] [PubMed] [Google Scholar]
  11. MITTERMAYER C., BRAUN R., RUSCH H. P. THE EFFECT OF ACTINOMYCIN D ON THE TIMING OF MITOSIS IN PHYSARUM POLYCEPHALUM. Exp Cell Res. 1965 Apr;38:33–41. doi: 10.1016/0014-4827(65)90424-6. [DOI] [PubMed] [Google Scholar]
  12. Maekawa S., Sakai H. Characterization and in vitro polymerization of Tetrahymena tubulin. J Biochem. 1978 Apr;83(4):1065–1075. doi: 10.1093/oxfordjournals.jbchem.a131995. [DOI] [PubMed] [Google Scholar]
  13. O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
  14. Osley M. A., Sheffery M., Newton A. Regulation of flagellin synthesis in the cell cycle of caulobacter: dependence on DNA replication. Cell. 1977 Oct;12(2):393–400. doi: 10.1016/0092-8674(77)90115-5. [DOI] [PubMed] [Google Scholar]
  15. Riddle V. G., Dubrow R., Pardee A. B. Changes in the synthesis of actin and other cell proteins after stimulation of serum-arrested cells. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1298–1302. doi: 10.1073/pnas.76.3.1298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Roobol A., Pogson C. I., Gull K. In vitro assembly of microtubule proteins from myxamoebae of Physarum polycephalum. Exp Cell Res. 1980 Nov;130(1):203–215. doi: 10.1016/0014-4827(80)90057-9. [DOI] [PubMed] [Google Scholar]
  17. Rusch H. P., Sachsenmaier W., Behrens K., Gruter V. Synchronization of mitosis by the fusion of the plasmodia of Physarum polycephalum. J Cell Biol. 1966 Oct;31(1):204–209. doi: 10.1083/jcb.31.1.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Sheir-Neiss G., Lai M. H., Morris N. R. Identification of a gene for beta-tubulin in Aspergillus nidulans. Cell. 1978 Oct;15(2):639–647. doi: 10.1016/0092-8674(78)90032-6. [DOI] [PubMed] [Google Scholar]
  19. Weeks D. P., Collis P. S. Induction and synthesis of tubulin during the cell cycle and life cycle of Chlamydomonas reinhardi. Dev Biol. 1979 Apr;69(2):400–407. doi: 10.1016/0012-1606(79)90300-2. [DOI] [PubMed] [Google Scholar]

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