Rajpurohit Yogendra Singh, Lal Mitu, Sharma Dhirendra Kumar, Soni Ishu
Molecular Biology Division, Bhabha Atomic Research Centre, 2-46-S, Modular Lab, A-Block, Mumbai, 400085, India.
Homi Bhabha National Institute (DAE-Deemed University), Mumbai, 400094, India.
Mol Cell Biochem. 2025 May 23. doi: 10.1007/s11010-025-05291-2.
The maintenance of genomic stability is crucial for life, threatened by DNA damage from both endogenous and exogenous sources. Cells employ DNA damage response through various repair mechanisms and DNA damage tolerance via translesion synthesis (TLS), to bypass DNA lesions and prevent replication fork collapse. This review explores the roles of human TLS polymerases in navigating replication stress, a critical process that can lead to genomic instability and cancer. It discusses TLS polymerase's dual role in genome preservation under certain physiological conditions while may also contribute to adaptive mutagenesis, highlighting their significance in DNA damage tolerance, somatic hypermutations, and cancer therapeutics. Understanding these mechanisms offers insights for developing targeted cancer therapies.
基因组稳定性的维持对生命至关重要,它受到内源性和外源性来源的DNA损伤的威胁。细胞通过各种修复机制进行DNA损伤应答,并通过跨损伤合成(TLS)实现DNA损伤耐受,以绕过DNA损伤并防止复制叉崩溃。本综述探讨了人类TLS聚合酶在应对复制应激中的作用,复制应激是一个关键过程,可导致基因组不稳定和癌症。它讨论了TLS聚合酶在某些生理条件下在基因组保存中的双重作用,同时也可能导致适应性诱变,强调了它们在DNA损伤耐受、体细胞高频突变和癌症治疗中的重要性。了解这些机制为开发靶向癌症治疗提供了思路。