DNA Damage Response Group, Basic Medical Science, St George's University of London, Cranmer Terrace, Tooting, London SW17 0RE, UK.
Biochem Soc Trans. 2010 Feb;38(Pt 1):87-91. doi: 10.1042/BST0380087.
The DDR (DNA damage response) is a signalling transduction cascade utilizing many forms of post-translation modification of proteins, including phosphorylation and ubiquitination. The well-known function of ubiquitination is to target proteins for proteasomal degradation; however, it is also involved in the regulation of protein function. The present review describes how ubiquitination regulates the function of certain proteins involved in DDR, in particular FANCD2 (Fanconi's anaemia complementation group D2) and PCNA (proliferating-cell nuclear antigen). Also, the proteomic methods currently used to identify new ubiquitinated proteins in response to DNA damage, including the advantages of using the UBD (ubiquitin-binding domain) beads to purify the ubiquitinated proteins, are considered.
DDR(DNA 损伤反应)是一个信号转导级联反应,利用蛋白质的多种翻译后修饰形式,包括磷酸化和泛素化。泛素化的一个众所周知的功能是将蛋白质靶向蛋白酶体降解;然而,它也参与了蛋白质功能的调节。本综述描述了泛素化如何调节 DDR 中某些蛋白质的功能,特别是 FANCD2(范可尼贫血互补组 D2)和 PCNA(增殖细胞核抗原)。此外,还考虑了目前用于鉴定 DNA 损伤反应中新型泛素化蛋白质的蛋白质组学方法,包括使用 UBD(泛素结合域)珠来纯化泛素化蛋白质的优点。