McPherson Matthew T, Holub Ashton S, Husbands Aman Y, Petreaca Ruben C
Department of Molecular Genetics, The Ohio State University, Columbus, OH 43215, USA.
Cancers (Basel). 2020 Dec 16;12(12):3794. doi: 10.3390/cancers12123794.
The MRN complex (MRE11, RAD50, NBS1/NBN) is a DNA double strand break sensor in eukaryotes. The complex directly participates in, or coordinates, several activities at the break such as DNA resection, activation of the DNA damage checkpoint, chromatin remodeling and recruitment of the repair machinery. Mutations in components of the MRN complex have been described in cancer cells for several decades. Using the Catalogue of Somatic Mutations in Cancer (COSMIC) database, we characterized all the reported MRN mutations. This analysis revealed several hotspot frameshift mutations in all three genes that introduce premature stop codons and truncate large regions of the C-termini. We also found through evolutionary analyses that COSMIC mutations are enriched in conserved residues of NBS1/NBN and RAD50 but not in MRE11. Given that all three genes are important to carcinogenesis, we propose these differential enrichment patterns may reflect a more severe pleiotropic role for MRE11.
MRN复合物(MRE11、RAD50、NBS1/NBN)是真核生物中的一种DNA双链断裂传感器。该复合物直接参与或协调断裂处的多种活动,如DNA切除、DNA损伤检查点的激活、染色质重塑以及修复机制的招募。几十年来,癌细胞中已发现MRN复合物各组分的突变。利用癌症体细胞突变目录(COSMIC)数据库,我们对所有已报道的MRN突变进行了特征分析。该分析揭示了所有三个基因中的几个热点移码突变,这些突变引入了过早的终止密码子并截断了C末端的大片区域。我们还通过进化分析发现,COSMIC突变在NBS1/NBN和RAD50的保守残基中富集,而在MRE11中未富集。鉴于这三个基因对致癌作用都很重要,我们认为这些不同的富集模式可能反映了MRE11更严重的多效性作用。