Revisiting retinoblastoma protein phosphorylation during the mammalian cell cycle |
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Authors: | S. Cooper J.A. Shayman |
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Affiliation: | (1) Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor (Michigan 48109-0620, USA), Fax +1 734 764 3562, e-mail: cooper@umich.edu, US;(2) Nephrology Division, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor (Michigan 48109-0676, USA), e-mail: jshayman@umich.edu, US |
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Abstract: | ![]() It is widely accepted that phosphorylation of the retinoblastoma (Rb) protein during the G1 phase of the mammalian division cycle is a major control element regulating passage of cells into S phase and through the division cycle. The experiments supporting G1-phase-specific Rb phosphorylation and the historical development of this idea are reviewed. By making a rigorous distinction between 'growth cessation' and the phenomena of 'cell cycle exit' or 'G1-phase arrest', the evidence for the G1-phase-specific phosphorylation of Rb protein is reinterpreted. We show that the evidence for G1-phase phosphorylation of Rb rests on few experiments and a chain of reasoning with some weak links. Evidence is reviewed that growth conditions regulate the phosphorylation of Rb. A growth-regulated control system that is independent of the cell cycle explains much of the evidence adduced to support cycle-specific phosphorylation of Rb. We propose that additional experimental evidence is needed to decide whether there is a G1-phase-specific phosphorylation of Rb protein. Received 16 October 2000; received after revision 13 November 2000; accepted 15 November 2000 |
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Keywords: | . G1 phase cell cycle G1-phase arrest phosphorylation. |
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