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首页> 外文期刊>Cellular & molecular biology letters. >LATENT VIRUSES CAN CAUSE DISEASE BY DISRUPTING THE COMPETITION FOR THE LIMITING FACTOR p300/CBP
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LATENT VIRUSES CAN CAUSE DISEASE BY DISRUPTING THE COMPETITION FOR THE LIMITING FACTOR p300/CBP

机译:潜在病毒可通过破坏限制因子p300 / CBP的竞争而引起疾病

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CBP and p300 are histone acetyltransferase coactivators that control the transcription of numerous genes in humans, viruses, and other organisms. Although two separate genes encode CBP and p300, they share a 61% sequence identity, and they are often mentioned together as p300/CBP. Zhou et al. showed that under hypoxic conditions, HIF1α and the tumor suppressor p53 compete for binding to the limiting p300/CBP coactivator. Jethanandani & Kramer showed that δEF1 and MYOD genes compete for the limited amount of p300/CBP in the cell. Bhattacharyya et al. showed that the limiting availability of p300/CBP in the cell serves as a checkpoint for HIF1α activity. Here, we use the microcompetition model to explain how latent viruses with a specific viral cis-regulatory element in their promoter/enhancer can disrupt this competition, causing diseases such as cancer, diabetes, atherosclerosis, and obesity.
机译:CBP和p300是组蛋白乙酰转移酶共激活因子,可控制人类,病毒和其他生物中众多基因的转录。尽管两个单独的基因编码CBP和p300,但它们具有61%的序列同一性,并且经常一起被称为p300 / CBP。周等。结果表明,在缺氧条件下,HIF1α和肿瘤抑制因子p53竞争与限制性p300 / CBP共激活因子的结合。 Jethanandani&Kramer表明δEF1和MYOD基因竞争细胞中有限数量的p300 / CBP。 Bhattacharyya等。结果表明,细胞中p300 / CBP的有限可用性是HIF1α活性的检查点。在这里,我们使用微竞争模型来解释在其启动子/增强子中具有特定病毒顺式调控元件的潜伏病毒如何破坏这种竞争,从而导致诸如癌症,糖尿病,动脉粥样硬化和肥胖症等疾病。

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