p16/CKDN2A位点的替代产物连接Rb和p53肿瘤抑制因子。

M C James, G Peters
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引用次数: 21

摘要

CDKN2A位点,p16INK4a细胞周期蛋白依赖性激酶抑制剂和一种称为ARF的蛋白指定了两种不同的产物。ARF已被证明与Mdm2-p53复合物结合,导致两种蛋白的稳定,并且存在一个反馈回路,通过该反馈回路,ARF水平受到p53的负调控。值得注意的是,ARF的表达受到转录因子E2F家族成员的正调控。这提供了Rb和p53途径之间的联系,以及Rb失活和E2F释放将导致p53稳定和功能激活的机制。编码ARF功能性氨基末端部分的另一个外显子可能代表了一个与p16INK4a共定位的独立基因,以利用共同的调控机制或目的。
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Alternative product of the p16/CKDN2A locus connects the Rb and p53 tumor suppressors.

Two distinct products are specified by the CDKN2A locus, the p16INK4a cyclin dependent kinase inhibitor and a protein termed ARF. ARF has been shown to bind to the Mdm2-p53 complex, resulting in stabilisation of both proteins, and a feedback loop exists through which ARF levels are negatively regulated by p53. Significantly, ARF expression is positively regulated by members of the E2F family of transcription factors. This provides a link between the Rb and p53 pathways and a mechanism whereby inactivation of Rb and release of E2F will lead to the stabilisation and functional activation of p53. The alternative exon encoding the functional amino terminal portion of ARF presumably represents an independent gene that has become co-localized with p16INK4a in order to exploit a common regulatory mechanism or purpose.

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