Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1983 May;154(2):702–707. doi: 10.1128/jb.154.2.702-707.1983

Podospora mutant defective in glucose-dependent growth control.

P Durrens
PMCID: PMC217519  PMID: 6841314

Abstract

A mutation (modE), previously described as a membrane mutation, results in several modifications of the female developmental cycle: a high density of protoperithecia, the unscheduled development of protoperithecia into sterile perithecia on the homokaryons of each mating type, and the independence of ascospore outgrowth from the substances normally required for germination. Cultured in liquid medium, the modE strain showed two additional specific features: a higher growth yield than that of wild-type cultures (plus 10% of dry weight) and an extreme reduction of cell life span. Both mutant traits were specific to glucose limitation. Despite the large difference existing in the sensitivity of cells to glucose starvation, the glycogen and trehalose reserves of mutant and wild-type cells were nearly identical. Considered together, these results suggest that the primary effect of the mutation lies in the disruption of a glucose-dependent regulation controlling the transition of the metabolic pattern of cells from growth to quiescence.

Full text

PDF
702

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boucherie H., Bernet J. Protoplasmic Incompatibility in PODOSPORA ANSERINA: a Possible Function for Incompatibility Genes. Genetics. 1980 Oct;96(2):399–411. doi: 10.1093/genetics/96.2.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boucherie H., Bernet J. Protoplasmic incompatibility and female organ formation in Podospora anserina: Properties of mutations abolishing both processes. Mol Gen Genet. 1974;135(2):163–174. doi: 10.1007/BF00264783. [DOI] [PubMed] [Google Scholar]
  3. Bürk R. R. One-step growth cycle for BHK21-13 hamster fibroblasts. Exp Cell Res. 1970 Dec;63(2):309–316. doi: 10.1016/0014-4827(70)90218-1. [DOI] [PubMed] [Google Scholar]
  4. Campisi J., Medrano E. E., Morreo G., Pardee A. B. Restriction point control of cell growth by a labile protein: evidence for increased stability in transformed cells. Proc Natl Acad Sci U S A. 1982 Jan;79(2):436–440. doi: 10.1073/pnas.79.2.436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Durrens P., Laigret F., Labarère J., Bernet J. Podospora anserina mutant defective in protoperithecium formation, ascospore germination, and cell regeneration. J Bacteriol. 1979 Dec;140(3):835–842. doi: 10.1128/jb.140.3.835-842.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Glinos A. D., Werrlein R. J. Density dependent regulation of growth in suspension cultures of L-929 cells. J Cell Physiol. 1972 Feb;79(1):79–90. doi: 10.1002/jcp.1040790109. [DOI] [PubMed] [Google Scholar]
  7. Gorin P. A., Spencer J. F. Structural chemistry of fungal polysaccharides. Adv Carbohydr Chem Biochem. 1968;23:367–417. doi: 10.1016/s0096-5332(08)60172-1. [DOI] [PubMed] [Google Scholar]
  8. Gunja-Smith Z., Patil N. B., Smith E. E. Two pools of glycogen in Saccharomyces. J Bacteriol. 1977 May;130(2):818–825. doi: 10.1128/jb.130.2.818-825.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Johnston G. C., Singer R. A., McFarlane S. Growth and cell division during nitrogen starvation of the yeast Saccharomyces cerevisiae. J Bacteriol. 1977 Nov;132(2):723–730. doi: 10.1128/jb.132.2.723-730.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Labarere J., Bernet J. Protoplasmic Incompatibility in PODOSPORA ANSERINA: A Possible Role for Its Associated Proteolytic Activity. Genetics. 1979 Nov;93(3):525–537. doi: 10.1093/genetics/93.3.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lillie S. H., Pringle J. R. Reserve carbohydrate metabolism in Saccharomyces cerevisiae: responses to nutrient limitation. J Bacteriol. 1980 Sep;143(3):1384–1394. doi: 10.1128/jb.143.3.1384-1394.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Medrano E. E., Pardee A. B. Prevalent deficiency in tumor cells of cycloheximide-induced cycle arrest. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4123–4126. doi: 10.1073/pnas.77.7.4123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pardee A. B. A restriction point for control of normal animal cell proliferation. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1286–1290. doi: 10.1073/pnas.71.4.1286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Piñon R. Folded chromosomes in non-cycling yeast cells: evidence for a characteristic g0 form. Chromosoma. 1978 Jul 31;67(3):263–274. doi: 10.1007/BF02569039. [DOI] [PubMed] [Google Scholar]
  15. Piñon R., Salts Y. Isolation of folded chromosomes from the yeast Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1977 Jul;74(7):2850–2854. doi: 10.1073/pnas.74.7.2850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Rossow P. W., Riddle V. G., Pardee A. B. Synthesis of labile, serum-dependent protein in early G1 controls animal cell growth. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4446–4450. doi: 10.1073/pnas.76.9.4446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Smith D., Muscatine L., Lewis D. Carbohydrate movement from autotrophs to heterotrophs in parasitic and mutualistic symbiosis. Biol Rev Camb Philos Soc. 1969 Feb;44(1):17–90. doi: 10.1111/j.1469-185x.1969.tb00821.x. [DOI] [PubMed] [Google Scholar]
  18. Stoker M. G. The Leeuwenhoek lecture, 1971. Tumour viruses and the sociology of fibroblasts. Proc R Soc Lond B Biol Sci. 1972 Apr 18;181(1062):1–17. doi: 10.1098/rspb.1972.0038. [DOI] [PubMed] [Google Scholar]
  19. Studzinski G. P., Gierthy J. F. Selective inhibition of the cell cycle of cultured human diploid fibroblasts by aminonucleoside of puromycin. J Cell Physiol. 1973 Feb;81(1):71–83. doi: 10.1002/jcp.1040810109. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES