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・ Cycling at the 1964 Summer Olympics – Men's individual road race
・ Cycling at the 1964 Summer Olympics – Men's sprint
・ Cycling at the 1964 Summer Olympics – Men's tandem
・ Cycling at the 1964 Summer Olympics – Men's team pursuit
・ Cycling at the 1964 Summer Olympics – Men's team time trial
・ Cycling at the 1967 Pan American Games
・ Cycling at the 1968 Summer Olympics
・ Cycling at the 1968 Summer Olympics – Men's 1000m time trial
・ Cycling at the 1968 Summer Olympics – Men's individual pursuit
・ Cycling at the 1968 Summer Olympics – Men's individual road race
・ Cycling at the 1968 Summer Olympics – Men's sprint
・ Cycling at the 1968 Summer Olympics – Men's tandem
・ Cycling at the 1968 Summer Olympics – Men's team pursuit
・ Cycling at the 1968 Summer Olympics – Men's team time trial
・ Cycling at the 1970 Asian Games
Cyclin E
・ Cyclin E1
・ Cyclin E2
・ Cyclin H
・ Cyclin K
・ Cyclin O
・ Cyclin T1
・ Cyclin T2
・ Cyclin-dependent kinase
・ Cyclin-dependent kinase 1
・ Cyclin-dependent kinase 10
・ Cyclin-dependent kinase 2
・ Cyclin-dependent kinase 3
・ Cyclin-dependent kinase 4
・ Cyclin-dependent kinase 5


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Cyclin E : ウィキペディア英語版
Cyclin E

Cyclin E is a member of the cyclin family.
Cyclin E binds to G1 phase Cdk2, which is required for the transition from G1 to S phase of the cell cycle that determines cell division. The Cyclin E/CDK2 complex phosphorylates p27Kip1 (an inhibitor of Cyclin D), tagging it for degradation, thus promoting expression of Cyclin A, allowing progression to S phase.
==Functions of Cyclin E==
Like all cyclin family members, cyclin E forms a complex with cyclin-dependent kinase (CDK2). Cyclin E/CDK2 regulates multiple cellular processes by phosphorylating numerous downstream proteins.
Cyclin E/CDK2 plays a critical role in the G1 phase and in the G1-S phase transition. Cyclin E/CDK2 phosphorylates retinoblastoma protein (Rb) to promote G1 progression. Hyper-phosphorylated Rb will no longer interact with E2F transcriptional factor, thus release it to promote expression of genes that drive cells to S phase through G1 phase.〔Hinds PW, Mittnacht S, Dulic V, et al. Regulation of retinoblastoma protein functions by ectopic expression of human cyclins. Cell. 1992, 70: 993-1006〕 Cyclin E/CDK2 also phosphorylates p27 and p21 during G1 and S phases, respectively. Smad3, a key mediator of TGF-β pathway which inhibits cell cycle progression, can be phosphorylated by cyclin E/CDK2. The phosphorylation of Smad3 by cyclin E/CDK2 inhibits its transcriptional activity and ultimately facilitates cell cycle progression.〔Cooley A, Zelivianski S, Jeruss JS. Impact of cyclin E overexpression on Smad3 activity in breast cancer cell lines. Cell Cycle. 2010, 9: 4900-4907〕 CBP/p300 and E2F-5 are also substrates of cyclin E/CDK2. Phosphorylation of these two proteins stimulates the transcriptional events during cell cycle progression.〔Morris L, Allen KE, La Thangue NB. Regulation of E2F transcription by cyclin E-Cdk2 kinase mediated through p300/CBP co-activators. Nat Cell Biol. 2000, 2: 232-239〕 Cyclin E/CDK2 can phosphorylate p220(NPAT) to promote histone gene transcription during cell cycle progression.〔Ma T, Van Tine BA, Wei Y, et al. Cell cycle-regulated phosphorylation of p220(NPAT) by cyclin E/Cdk2 in Cajal bodies promotes histone gene transcription. Genes Dev. 2000, 14: 2298-2313〕
Apart from the function in cell cycle progression, cyclin E/CDK2 plays a role in the centrosome cycle. This function is performed by phosphorylating nucleophosmin (NPM). Then NPM is released from binding to an unduplicated centrosome, thereby triggering duplication.〔Okuda M, Horn HF, Tarapore P, et al. Nucleophosmin/B23 is a target of CDK2/cyclin E in centrosome duplication. Cell 2000, 103: 127-140〕 CP110 is another cyclin E/CDK2 substrate which involves in centriole duplication and centrosome separation.〔Chen Z, Indjeian VB, McManus M, et al. CP110, a cell cycle-dependent CDK substrate, regulates centrosome duplication in human cells. Dev Cell. 2002, 3: 339-350〕 Cyclin E/CDK2 has also been shown to regulate the apoptotic response to DNA damage via phosphorylation of FOXO1.〔Huang H, Regan KM, Lou Z, et al. Cdk2-dependent phosphorylation of FOXO1 as an apoptotic response to DNA damage. Science. 2006, 314: 294-297〕

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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