Difference between revisions of "3187043"

From CellBiology
(pRb)
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--[[User:S8600021|Mark Hill]] 18:58, 12 May 2009 (EST)Your individual project (due week 10) needs significant work.
 
  
==Individual Project==
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'''Retinoblastoma Protein'''
  
Rb Protein
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named from a chidhood cancer where it was first discovered
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rb inhibits the cell cycle
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becomes inactive when it is phosphorylated by protein cyclin-dependent kinases Cdk4 and Cdk2, unblocking and allowing the cell to pass the restriction point in order to progress from the G1 phase into the S phase of the cell cycle. Prior to this crutial step, the activation of Cdk4 and Cdk2 must occur through the synthesis and binding of cyclins D and E to Cdk4 and Cdk2, respectively, which form cyclin-cdk complexes.
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Purves et al. Life The Science Of Biology 7E
  
 
"previous studies indicate that the HCV RNA-dependent RNA polymerase, nonstructural protein 5B (NS5B), forms a complex with the retinoblastoma tumor suppressor protein (pRb), targeting it for degradation, activating E2F-responsive promoters, and stimulating cellular proliferation....the abundance of pRb is strongly downregulated, and its normal nuclear localization altered to include a major cytoplasmic component..."
 
"previous studies indicate that the HCV RNA-dependent RNA polymerase, nonstructural protein 5B (NS5B), forms a complex with the retinoblastoma tumor suppressor protein (pRb), targeting it for degradation, activating E2F-responsive promoters, and stimulating cellular proliferation....the abundance of pRb is strongly downregulated, and its normal nuclear localization altered to include a major cytoplasmic component..."

Revision as of 16:39, 13 May 2009

Retinoblastoma Protein

named from a chidhood cancer where it was first discovered rb inhibits the cell cycle becomes inactive when it is phosphorylated by protein cyclin-dependent kinases Cdk4 and Cdk2, unblocking and allowing the cell to pass the restriction point in order to progress from the G1 phase into the S phase of the cell cycle. Prior to this crutial step, the activation of Cdk4 and Cdk2 must occur through the synthesis and binding of cyclins D and E to Cdk4 and Cdk2, respectively, which form cyclin-cdk complexes.

Purves et al. Life The Science Of Biology 7E

"previous studies indicate that the HCV RNA-dependent RNA polymerase, nonstructural protein 5B (NS5B), forms a complex with the retinoblastoma tumor suppressor protein (pRb), targeting it for degradation, activating E2F-responsive promoters, and stimulating cellular proliferation....the abundance of pRb is strongly downregulated, and its normal nuclear localization altered to include a major cytoplasmic component..."

http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2323300&tool=pmcentrez&rendertype=abstract

Structure-function analysis of the retinoblastoma tumor suppressor protein – is the whole a sum of its parts?

Human papillomavirus immortalization and transformation functions