Lavin Martin F
Queensland Cancer Fund Research Unit, Queensland Institute of Medical Research, P.O. Box Royal Brisbane Hospital, Herston, Brisbane, Qld 4029, Australia.
DNA Repair (Amst). 2004 Nov 2;3(11):1515-20. doi: 10.1016/j.dnarep.2004.07.001.
Mutations in components of the Mre11/Rad50/Nbs1 complex give rise to genetic disorders characterized by neurological abnormalities, radiosensitivity, cell cycle checkpoint defects, genomic instability and cancer predisposition. Evidence exists that this complex associates with chromatin during DNA replication and acts as a sensor of double strand breaks (dsbs) in DNA after exposure to radiation. A series of recent reports provides additional support that the complex senses breaks in DNA and relays this information to ATM, mutated in ataxia-telangiectasia (A-T), which in turn activates pathways for cell cycle checkpoint activation. Paradoxically members of the Mre11 complex are also downstream of ATM in these pathways. Here, Lavin attempts to make sense of this sensing mechanism with reference to a series of recent reports on the topic.
Mre11/Rad50/Nbs1复合物成分的突变会引发一些遗传性疾病,其特征包括神经异常、辐射敏感性、细胞周期检查点缺陷、基因组不稳定和癌症易感性。有证据表明,该复合物在DNA复制过程中与染色质结合,并在暴露于辐射后作为DNA双链断裂(dsb)的传感器。最近的一系列报告进一步支持了该复合物能够感知DNA断裂并将此信息传递给共济失调毛细血管扩张症(A-T)中发生突变的ATM,而ATM继而激活细胞周期检查点激活途径。矛盾的是,在这些途径中,Mre11复合物的成员也处于ATM的下游。在此,拉文试图参考最近一系列关于该主题的报告来解读这种传感机制。