Please use this identifier to cite or link to this item: https://doi.org/10.1042/BSR20160152
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dc.titleAPC/C and retinoblastoma interaction: cross-talk of retinoblastoma protein with the ubiquitin proteasome pathway
dc.contributor.authorRamanujan, Ajeena
dc.contributor.authorTiwari, Swati
dc.date.accessioned2022-04-13T05:40:48Z
dc.date.available2022-04-13T05:40:48Z
dc.date.issued2016-10-01
dc.identifier.citationRamanujan, Ajeena, Tiwari, Swati (2016-10-01). APC/C and retinoblastoma interaction: cross-talk of retinoblastoma protein with the ubiquitin proteasome pathway. BIOSCIENCE REPORTS 36 (5). ScholarBank@NUS Repository. https://doi.org/10.1042/BSR20160152
dc.identifier.issn0144-8463
dc.identifier.issn1573-4935
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/219116
dc.description.abstractThe ubiquitin (Ub) ligase anaphase promoting complex/cyclosome (APC/C) and the tumour suppressor retinoblastoma protein (pRB) play key roles in cell cycle regulation. APC/C is a critical regulator of mitosis and G1-phase of the cell cycle whereas pRB keeps a check on proliferation by inhibiting transition to the S-phase. APC/C and pRB interact with each other via the co-activator of APC/C, FZR1, providing an alternative pathway of regulation of G1 to S transition by pRB using a post-translational mechanism. Both pRB and FZR1 have complex roles and are implicated not only in regulation of cell proliferation but also in differentiation, quiescence, apoptosis, maintenance of chromosomal integrity and metabolism. Both are also targeted by transforming viruses. We discuss recent advances in our understanding of the involvement of APC/C and pRB in cell cycle based decisions and how these insights will be useful for development of anti-cancer and anti-viral drugs.
dc.language.isoen
dc.publisherPORTLAND PRESS LTD
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiochemistry & Molecular Biology
dc.subjectCell Biology
dc.subjectanaphase promoting complex/cyclosome
dc.subjectcell cycle
dc.subjectFZR1
dc.subjecthuman papilloma virus
dc.subjectLxCxE
dc.subjectretinoblastoma
dc.subjectANAPHASE-PROMOTING COMPLEX
dc.subjectPAPILLOMAVIRUS TYPE-16 E7
dc.subjectCELL-CYCLE PROGRESSION
dc.subjectTUMOR-SUPPRESSOR
dc.subjectLOW-PENETRANCE
dc.subjectGENE-PRODUCT
dc.subjectCOMPLEX/CYCLOSOME APC/C
dc.subjectS-PHASE
dc.subjectD-BOX
dc.subjectTRANSCRIPTIONAL REPRESSOR
dc.typeReview
dc.date.updated2022-04-13T03:39:49Z
dc.contributor.departmentPHYSIOLOGY
dc.description.doi10.1042/BSR20160152
dc.description.sourcetitleBIOSCIENCE REPORTS
dc.description.volume36
dc.description.issue5
dc.published.statePublished
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