The retinoblastoma family of proteins and their regulatory functions in the mammalian cell division cycle
被引:210
作者:
Henley, Shauna A.
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Univ Western Ontario, London Reg Canc Program, London, ON, Canada
Univ Western Ontario, Dept Biochem, London, ON, Canada
Grande Prairie Coll, Grande Prairie, AB, CanadaUniv Western Ontario, London Reg Canc Program, London, ON, Canada
Henley, Shauna A.
[1
,3
,4
]
Dick, Frederick A.
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Univ Western Ontario, London Reg Canc Program, London, ON, Canada
Univ Western Ontario, Childrens Hlth Res Inst, London, ON, Canada
Univ Western Ontario, Dept Biochem, London, ON, CanadaUniv Western Ontario, London Reg Canc Program, London, ON, Canada
Dick, Frederick A.
[1
,2
,3
]
机构:
[1] Univ Western Ontario, London Reg Canc Program, London, ON, Canada
[2] Univ Western Ontario, Childrens Hlth Res Inst, London, ON, Canada
[3] Univ Western Ontario, Dept Biochem, London, ON, Canada
[4] Grande Prairie Coll, Grande Prairie, AB, Canada
The retinoblastoma (RB) family of proteins are found in organisms as distantly related as humans, plants, and insects. These proteins play a key role in regulating advancement of the cell division cycle from the G1 to S-phases. This is achieved through negative regulation of two important positive regulators of cell cycle entry, E2F transcription factors and cyclin dependent kinases. In growth arrested cells transcriptional activity by E2Fs is repressed by RB proteins. Stimulation of cell cycle entry by growth factor signaling leads to activation of cyclin dependent kinases. They in turn phosphorylate and inactivate the RB family proteins, leading to E2F activation and additional cyclin dependent kinase activity. This propels the cell cycle irreversibly forward leading to DNA synthesis. This review will focus on the basic biochemistry and cell biology governing the regulation and activity of mammalian RB family proteins in cell cycle control.
机构:
Univ Toulouse, CNRS, LBCMCP, UMR5088, Toulouse, FranceFred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
Besson, Arnaud
;
Dowdy, Steven F.
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Univ Calif San Diego, Sch Med, Howard Hughes Med Inst, Dept Cellular & Mol Med, La Jolla, CA 92093 USAFred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
Dowdy, Steven F.
;
Roberts, James M.
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Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USAFred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
机构:
Univ Ottawa, Fac Med, Dept Microbiol & Immunol, Ottawa Inst Syst Biol & Biochem, Ottawa, ON K1H 8M5, CanadaNYU, Sch Med, Dept Pathol, New York, NY 10016 USA
Blais, Alexandre
;
Dynlacht, Brian D.
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NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
NYU, Sch Med, Inst Canc, New York, NY 10016 USANYU, Sch Med, Dept Pathol, New York, NY 10016 USA
机构:
Univ Toulouse, CNRS, LBCMCP, UMR5088, Toulouse, FranceFred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
Besson, Arnaud
;
Dowdy, Steven F.
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h-index: 0
机构:
Univ Calif San Diego, Sch Med, Howard Hughes Med Inst, Dept Cellular & Mol Med, La Jolla, CA 92093 USAFred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
Dowdy, Steven F.
;
Roberts, James M.
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h-index: 0
机构:
Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USAFred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
机构:
Univ Ottawa, Fac Med, Dept Microbiol & Immunol, Ottawa Inst Syst Biol & Biochem, Ottawa, ON K1H 8M5, CanadaNYU, Sch Med, Dept Pathol, New York, NY 10016 USA
Blais, Alexandre
;
Dynlacht, Brian D.
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机构:
NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
NYU, Sch Med, Inst Canc, New York, NY 10016 USANYU, Sch Med, Dept Pathol, New York, NY 10016 USA