McCulloch Scott D, Kunkel Thomas A
Department of Environmental and Molecular Toxicology, North Carolina State University, Campus Box 7633, Raleigh, NC 27695, USA.
Cell Res. 2008 Jan;18(1):148-61. doi: 10.1038/cr.2008.4.
In their seminal publication describing the structure of the DNA double helix, Watson and Crick wrote what may be one of the greatest understatements in the scientific literature, namely that "It has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material." Half a century later, we more fully appreciate what a huge challenge it is to replicate six billion nucleotides with the accuracy needed to stably maintain the human genome over many generations. This challenge is perhaps greater than was realized 50 years ago, because subsequent studies have revealed that the genome can be destabilized not only by environmental stresses that generate a large number and variety of potentially cytotoxic and mutagenic lesions in DNA but also by various sequence motifs of normal DNA that present challenges to replication. Towards a better understanding of the many determinants of genome stability, this chapter reviews the fidelity with which undamaged and damaged DNA is copied, with a focus on the eukaryotic B- and Y-family DNA polymerases, and considers how this fidelity is achieved.
在描述DNA双螺旋结构的开创性论文中,沃森和克里克写下了科学文献中或许最为低调的表述之一,即“我们注意到,我们所假设的特定配对方式立即暗示了遗传物质可能的复制机制。”半个世纪后,我们更充分地认识到,要以稳定维持人类基因组多代所需的准确性复制60亿个核苷酸是一项多么巨大的挑战。这项挑战或许比50年前所意识到的更大,因为后续研究表明,基因组不仅会因在DNA中产生大量且多样的潜在细胞毒性和诱变损伤的环境压力而变得不稳定,还会因正常DNA的各种序列基序给复制带来挑战而不稳定。为了更好地理解基因组稳定性的诸多决定因素,本章回顾了未受损和受损DNA的复制保真度,重点关注真核生物的B族和Y族DNA聚合酶,并探讨了如何实现这种保真度。