PP2A holoenzymes negatively and positively regulate cell cycle progression by dephosphorylating pocket proteins and multiple CDK substrates

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• 作者：Alison Kurimchak^a ; Xavier Grañ ; a^a ; ^b ; ^{xavier@temple.edu}
• 关键词：CDK ; cyclin dependent kinase ; CKI ; cyclin dependent kinase inhibitor ; PP1 ; protein phosphatase 1 ; PP2A ; protein phosphatase 2A ; RB ; retinoblastoma ; EGF ; epidermal growth factor ; HEAT ; Huntington ; elongation factor 3 ; PR65/A ; TOR ; GANP ; germinal center-ass
• 刊名：Gene
• 出版年：2012
• 期刊代码：73_03781119
• 类别：bio
• 出版时间：10 May, 2012
• 卷：499
• 期：1
• 页码：1-7
• 文件大小：533 K

摘要

Cell cycle progression is negatively regulated by the retinoblastoma family of pocket proteins and CDK inhibitors (CKIs). In contrast, CDKs promote progression through multiple phases of the cell cycle. One prominent way by which CDKs promote cell cycle progression is by inactivation of pocket proteins via hyperphosphorylation. Reactivation of pocket proteins to halt cell cycle progression requires dephosphorylation of multiple CDK-phosphorylated sites and is accomplished by PP2A and PP1 serine/threonine protein phosphatases. The same phosphatases are also implicated in dephosphorylation of multiple CDK substrates as cells exit mitosis and reenter the G1 phase of the cell cycle. This review is primarily focused on the role of PP2A and PP1 in the activation of pocket proteins during the cell cycle and in response to signaling cues that trigger cell cycle exit. Other functions of PP2A during the cell cycle will be discussed in brief, as comprehensive reviews on this topic have been published recently (De Wulf et al., 2009; Wurzenberger and Gerlich, 2011).