Tan Ban Xiong, Liew Hoe Peng, Chua Joy S, Ghadessy Farid J, Tan Yaw Sing, Lane David P, Coffill Cynthia R
p53 Laboratory, Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, Immunos #06-06, Singapore138648, Singapore.
Bioinformatics Institute, Agency for Science, Technology and Research (A*STAR), 30 Biopolis St, #07-01,Singapore138671, Singapore.
J Mol Cell Biol. 2017 Feb 1;9(1):3-15. doi: 10.1093/jmcb/mjx002.
Mouse double minute (Mdm) genes span an evolutionary timeframe from the ancient eukaryotic placozoa Trichoplax adhaerens to Homo sapiens, implying a significant and possibly conserved cellular role throughout history. Maintenance of DNA integrity and response to DNA damage involve many key regulatory pathways, including precise control over the tumour suppressor protein p53. In most vertebrates, degradation of p53 through proteasomal targeting is primarily mediated by heterodimers of Mdm2 and the Mdm2-related protein Mdm4 (also known as MdmX). Both Mdm2 and Mdm4 have p53-binding regions, acidic domains, zinc fingers, and C-terminal RING domains that are conserved throughout evolution. Vertebrates typically have both Mdm2 and Mdm4 genes, while analyses of sequenced genomes of invertebrate species have identified single Mdm genes, suggesting that a duplication event occurred prior to emergence of jawless vertebrates about 550-440 million years ago. The functional relationship between Mdm and p53 in T. adhaerens, an organism that has existed for 1 billion years, implies that these two proteins have evolved together to maintain a conserved and regulated function.
小鼠双微体(Mdm)基因跨越了从古老的真核生物扁盘动物黏胶丝盘虫到智人的进化时间框架,这意味着在整个历史中它们具有重要且可能保守的细胞作用。DNA完整性的维持和对DNA损伤的反应涉及许多关键调控途径,包括对肿瘤抑制蛋白p53的精确控制。在大多数脊椎动物中,通过蛋白酶体靶向作用使p53降解主要由Mdm2和Mdm2相关蛋白Mdm4(也称为MdmX)的异二聚体介导。Mdm2和Mdm4都具有p53结合区域、酸性结构域、锌指结构以及在整个进化过程中保守的C端RING结构域。脊椎动物通常同时拥有Mdm2和Mdm4基因,而对无脊椎动物物种测序基因组的分析已鉴定出单个Mdm基因,这表明在约5.5亿至4.4亿年前无颌脊椎动物出现之前发生了一次基因复制事件。在已存在10亿年的黏胶丝盘虫中,Mdm与p53之间的功能关系表明这两种蛋白质共同进化以维持保守且受调控的功能。