Sansom Owen J, Maddison Kathryn, Clarke Alan R
Cardiff School of Biosciences, Cardiff University, Cardiff, UK.
Nat Clin Pract Oncol. 2007 May;4(5):305-15. doi: 10.1038/ncponc0812.
The methyl-CpG-binding domain (MBD) proteins 'read' and interpret the methylation moieties on DNA, and thus are critical mediators of many epigenetic processes. Currently, the MBD family comprises five members; MBD1, MBD2, MBD3, MBD4 and MeCP2. Although not a 'classical' MBD protein, Kaiso also mediates transcriptional repression by using zinc finger domains to bind its targets. Since DNA hypermethylation is a well-recognized mechanism underlying gene silencing events in both tumorigenesis and drug resistance, it is likely that the MBD proteins may be important modulators of tumorigenesis. We review the recent work addressing this possibility, and discuss several of the MBD proteins as potentially excellent novel therapeutic targets.
甲基化CpG结合结构域(MBD)蛋白“读取”并解读DNA上的甲基化部分,因此是许多表观遗传过程的关键调节因子。目前,MBD家族包含五个成员:MBD1、MBD2、MBD3、MBD4和MeCP2。尽管Kaiso不是一种“经典的”MBD蛋白,但它也通过利用锌指结构域结合其靶标来介导转录抑制。由于DNA高甲基化是肿瘤发生和耐药性中基因沉默事件的一种公认机制,MBD蛋白很可能是肿瘤发生的重要调节因子。我们回顾了针对这种可能性的近期研究工作,并讨论了几种MBD蛋白作为潜在的优秀新型治疗靶点。