Stephen Cooper

Summary

Affiliation: University of Michigan
Country: USA

Publications

  1. ncbi On a heuristic point of view concerning the expression of numerous genes during the cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA
    IUBMB Life 64:10-7. 2012
  2. ncbi Is whole-culture synchronization biology's 'perpetual-motion machine'?
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Trends Biotechnol 22:266-9. 2004
  3. ncbi Rejoinder: whole-culture synchronization cannot, and does not, synchronize cells
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor MI 48109 0620, USA
    Trends Biotechnol 22:274-6. 2004
  4. ncbi Control and maintenance of mammalian cell size
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    BMC Cell Biol 5:35. 2004
  5. ncbi Reanalysis of the protocol for in vitro synchronization of mammalian astrocytic cultures by serum deprivation
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Brain Res Brain Res Protoc 15:115-8. 2005
  6. ncbi Comment on and reply to "Analysis of variation of amplitudes in cell cycle gene expression" by Liu, Gaido and Wolfinger: on the analysis of gene expression during the normal, eukaryotic, cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Theor Biol Med Model 2:47. 2005
  7. ncbi Nocodazole does not synchronize cells: implications for cell-cycle control and whole-culture synchronization
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Cell Tissue Res 324:237-42. 2006
  8. ncbi Distinguishing between linear and exponential cell growth during the division cycle: single-cell studies, cell-culture studies, and the object of cell-cycle research
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Theor Biol Med Model 3:10. 2006
  9. ncbi Checkpoints and restriction points in bacteria and eukaryotic cells
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Bioessays 28:1035-9. 2006
  10. ncbi Regulation of DNA synthesis in bacteria: Analysis of the Bates/Kleckner licensing/initiation-mass model for cell cycle control
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Mol Microbiol 62:303-7. 2006

Collaborators

Detail Information

Publications37

  1. ncbi On a heuristic point of view concerning the expression of numerous genes during the cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA
    IUBMB Life 64:10-7. 2012
    ..An alternative view of the cell cycle proposes cycle-independent, invariant accumulation of mRNA during the cell cycle with decreases of specific proteins occurring only during the mitotic period of the cell cycle...
  2. ncbi Is whole-culture synchronization biology's 'perpetual-motion machine'?
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Trends Biotechnol 22:266-9. 2004
    ....
  3. ncbi Rejoinder: whole-culture synchronization cannot, and does not, synchronize cells
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor MI 48109 0620, USA
    Trends Biotechnol 22:274-6. 2004
    ....
  4. ncbi Control and maintenance of mammalian cell size
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    BMC Cell Biol 5:35. 2004
    ..If there is no cell-size-control system, then exponential growth is not allowed, as exponential growth, according to Conlon and Raff, would require a cell-size-control system...
  5. ncbi Reanalysis of the protocol for in vitro synchronization of mammalian astrocytic cultures by serum deprivation
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Brain Res Brain Res Protoc 15:115-8. 2005
    ..Thus, the proposed protocol will not produce a synchronized culture...
  6. ncbi Comment on and reply to "Analysis of variation of amplitudes in cell cycle gene expression" by Liu, Gaido and Wolfinger: on the analysis of gene expression during the normal, eukaryotic, cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Theor Biol Med Model 2:47. 2005
    ..are discussed in order to see whether their analysis is related to gene expression during the division cycle...
  7. ncbi Nocodazole does not synchronize cells: implications for cell-cycle control and whole-culture synchronization
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Cell Tissue Res 324:237-42. 2006
    ..The current view of cell-cycle control that is based on methods that are not suitable for cell-cycle analysis must therefore be reconsidered when results are based on whole-culture synchronization...
  8. ncbi Distinguishing between linear and exponential cell growth during the division cycle: single-cell studies, cell-culture studies, and the object of cell-cycle research
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Theor Biol Med Model 3:10. 2006
    ..In contrast to Mitchison's viewpoint, it is argued here that the biological laws underlying cell growth are not to be found in single-cell studies. The cellular growth law can and should be understood by studying cells as an aggregate...
  9. ncbi Checkpoints and restriction points in bacteria and eukaryotic cells
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Bioessays 28:1035-9. 2006
    ..Some of the ubiquitous checkpoint phenomena widely described may be merely the result of the inherent incompleteness of earlier events preventing the initiation of subsequent events...
  10. ncbi Regulation of DNA synthesis in bacteria: Analysis of the Bates/Kleckner licensing/initiation-mass model for cell cycle control
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Mol Microbiol 62:303-7. 2006
    ....
  11. ncbi Membrane-elution analysis of content of cyclins A, B1, and E during the unperturbed mammalian cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Cell Div 2:28. 2007
    ..The membrane-elution method is a method that allows the study of the cell cycle by producing a culture of unperturbed, synchronized cells...
  12. ncbi Microarrays and the relationship of mRNA variation to protein variation during the cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    J Theor Biol 249:574-81. 2007
    ..We conclude that mRNA variations during the division cycle, as measured by microarrays, cannot by themselves, identify cycle-specific functions related to protein variations...
  13. ncbi Thymidine block does not synchronize L1210 mouse leukaemic cells: implications for cell cycle control, cell cycle analysis and whole-culture synchronization
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Cell Prolif 41:156-67. 2008
    ..Generalizing the results to other cell lines, we suggest that these conclusions call into question experimental measurements of gene expression during the division cycle based on thymidine inhibition synchronization...
  14. ncbi On the use of metaphor to understand, explain, or rationalize redundant genes in yeast
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    FEMS Yeast Res 8:345-8; discussion 349-50. 2008
    ..The redundant gene proposal is analyzed, and it is noted that there are many problems with the redundant gene model. An alternative metaphor is suggested to explain the genetic composition of a yeast culture...
  15. ncbi On the fiftieth anniversary of the Schaechter, Maaløe, Kjeldgaard experiments: implications for cell-cycle and cell-growth control
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 5620, USA
    Bioessays 30:1019-24. 2008
    ..In particular, the emphasis on steady-state growth conditions, and clear and sharp changes in growth conditions were fundamental to their experiments and have been codified in the principles of the Copenhagen School of Microbiology...
  16. ncbi Experimental reconsideration of the utility of serum starvation as a method for synchronizing mammalian cells
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Cell Biol Int 33:71-7. 2009
    ....
  17. ncbi Invariant mRNA and mitotic protein breakdown solves the Russian Doll problem of the cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0520, USA
    Cell Biol Int 33:10-8. 2009
    ..These results, and theoretical ideas support an alternative view of the cell cycle where many of the proposed control systems do not exist...
  18. ncbi Rethinking synchronization of mammalian cells for cell cycle analysis
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Cell Mol Life Sci 60:1099-106. 2003
    ..Release of arrested cells from inhibition does not produce cells reflecting cells during the normal division cycle. Thus, cells produced by batch or forcing methods are not experimental models for analysis of the normal cell cycle...
  19. ncbi How the change from FLM to FACS affected our understanding of the G1-phase of the cell cycle
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0620, USA
    Cell Cycle 2:157-9. 2003
    ..It is suggested that these G1-phase controls and phenomena require a critical reevaluation in the light of an alternative cell-cycle model that does not require or postulate such G1-phase controls...
  20. ncbi Division pattern of a round mutant of Escherichia coli
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620, USA
    J Bacteriol 179:5582-4. 1997
    ..These results differ from a previous proposal that division planes in this round mutant are perpendicular to the prior division plane (W. D. Donachie, S. Addinall, and K. Begg, Bioessays 17:569-576, 1995)...
  21. ncbi On the interpretation of the shortening of the G1-phase by overexpression of cyclins in mammalian cells
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 49109 0620, USA
    Exp Cell Res 238:110-5. 1998
    ..Thus, the experiments on cyclin overexpression and their effect on G1-phase length cannot be used to support the proposal that cyclins act specifically during the G1-phase of the division cycle...
  22. ncbi On the proposal of a G0 phase and the restriction point
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 49109 0620, USA
    FASEB J 12:367-73. 1998
    ..Their experiments are consistent with the continuum model of the mammalian division cycle. There is no need to postulate a restriction point or a G0 phase to explain the serum starvation results...
  23. ncbi Mammalian cells are not synchronized in G1-phase by starvation or inhibition: considerations of the fundamental concept of G1-phase synchronization
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620, USA
    Cell Prolif 31:9-16. 1998
    ..However, these cells are not arrested at a particular point in the G1-phase. Analysis of 'G1 arrested cells' suggests that, upon resumption of growth, the cells are not synchronized...
  24. ncbi Cycle-specific replication of chromosomal and F-plasmid origins
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620, USA
    FEMS Microbiol Lett 163:217-22. 1998
    ....
  25. ncbi G1 and S phase gene expression cannot be analyzed in mammalian cells synchronized by inhibition
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, USA
    Microb Comp Genomics 2:269-73. 1997
    ..This proposal has a wide applicability and should not be confined to the specific article under discussion...
  26. ncbi Phosphorylation-dephosphorylation of retinoblastoma protein not necessary for passage through the mammalian cell division cycle
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620, USA
    IUBMB Life 48:225-30. 1999
    ..We propose that phosphorylation-dephosphorylation of Rb is independent of the division cycle and is primarily determined by growth conditions throughout the division cycle...
  27. ncbi Revisiting retinoblastoma protein phosphorylation during the mammalian cell cycle
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620, USA
    Cell Mol Life Sci 58:580-95. 2001
    ..We propose that additional experimental evidence is needed to decide whether there is a G1-phase-specific phosphorylation of Rb protein...
  28. ncbi Helical growth and the curved shape of Vibrio cholerae
    S Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620, USA
    FEMS Microbiol Lett 198:123-4. 2001
    ..The comma-like shape of V. cholerae is not due to an asymmetrical positioning of peptidoglycan such that some chains of peptidoglycan are placed so they are more spread out on one side of the cell and squeezed together on the other side...
  29. ncbi The Schaechter-Bentzon-Maaløe experiment and the analysis of cell cycle events in eukaryotic cells
    Stephen Cooper
    Dept of Microbiology, University of Michigan School of Medicine, Ann Arbor, MI 48109 0620, USA
    Trends Microbiol 10:169-73. 2002
    ..The idea of an control experiment under unperturbed conditions is proposed for the analysis of data on cell-cycle-specific gene expression in yeast and mammalian cells...
  30. ncbi Minimally disturbed, multicycle, and reproducible synchrony using a eukaryotic "baby machine"
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Bioessays 24:499-501. 2002
    ..But most important, the baby machine method now opens the way for the study of the cell cycle of minimally disturbed, artifact-free, well-synchronized, mammalian cells...
  31. ncbi Reappraisal of G1-phase arrest and synchronization by lovastatin
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    Cell Biol Int 26:715-27. 2002
    ..Analysis of previous reports of 'synchronization' and growth-arrest support these findings. It is concluded that lovastatin neither synchronizes cells, nor arrests cells in the G1-phase of the division cycle...
  32. ncbi Reappraisal of serum starvation, the restriction point, G0, and G1 phase arrest points
    Stephen Cooper
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109 0620, USA
    FASEB J 17:333-40. 2003
    ..It is proposed that the arrest of cells with a particular DNA content equivalent to that in cells in the G1 phase of the division cycle does not mean there is any particular G1 phase control point...
  33. ncbi Analysis of cell-cycle gene expression in Saccharomyces cerevisiae using microarrays and multiple synchronization methods
    Kerby Shedden
    Department of Statistics, University of Michigan, Ann Arbor, MI 48109 1285, USA
    Nucleic Acids Res 30:2920-9. 2002
    ..Under this alternative explanation, the observed cyclicities in the other three experiments are a stress response to synchronization, and may not reproduce in unperturbed cells...
  34. ncbi Analysis of cell-cycle-specific gene expression in human cells as determined by microarrays and double-thymidine block synchronization
    Kerby Shedden
    Department of Statistics, University of Michigan, Ann Arbor, MI 48109-1285, USA
    Proc Natl Acad Sci U S A 99:4379-84. 2002
    ..This finding places doubt on the assumption that the cells are actually synchronized. We propose that the microarray results do not support the proposal that there are numerous cell-cycle-specifically expressed genes in human cells...
  35. ncbi SDF-1alpha/CXCL12 enhances retroviral-mediated gene transfer into immature subsets of human and murine hematopoietic progenitor cells
    W Tao
    Department of Microbiology and Immunology, The Walther Oncology Center, Indiana University School of Medicine, Indianapolis, IN 46202-5181, USA
    Gene Ther 11:61-9. 2004
    ..These results may be of clinical relevance...
  36. ncbi Effect of mecillinam on peptidoglycan synthesis during the division cycle of Salmonella typhimurium 2616
    J Licht
    Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109 0620
    Res Microbiol 144:423-33. 1993
    ..Other antibiotics added at equivalent activities did not show an increase in cross-linking...
  37. ncbi Cell cycle analysis and microarrays
    Stephen Cooper
    Trends Genet 18:289-90. 2002