Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, United States.
Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, MN, 55455, United States.
DNA Repair (Amst). 2020 Oct;94:102875. doi: 10.1016/j.dnarep.2020.102875. Epub 2020 Jun 23.
Telomeres consist of repetitive tracts of DNA that shield a chromosome's contents from erosion and replicative attrition. However, telomeres are also late-replicating regions of the genome in which a myriad of replicative obstructions reside. The obstacles contained within telomeres, as well as their genomic location, drive replicative stalling and subsequent fork collapse in these regions. Consequently, large scale deletions, under-replicated DNA, translocations, and fusion events arise following telomere replication failure. Further, under-replicated DNA and telomere fusions that are permitted to enter mitosis will produce mitotic DNA bridges - known drivers of genetic loss and chromothripsis. Thus, aberrant telomere replication promotes genomic instability, which, in turn leads either to cellular death, senescence or oncogenic transformation. The importance of these issues for organismal well-being necessitates a need for resolute telomere maintenance. Here, we describe recent advances in identifying and understanding the molecular mechanisms that are in place in human cells to escort the replisome through the telomere's unwieldy structures and repetitive sequences. Finally, we review the pathways that combat the deleterious outcomes that occur when telomeric replication forks do collapse.
端粒由重复的 DNA 序列组成,这些序列可以保护染色体的内容免受侵蚀和复制损耗。然而,端粒也是基因组中复制较晚的区域,其中存在着无数的复制障碍。端粒中包含的障碍及其基因组位置会导致这些区域的复制停滞和随后的叉崩溃。因此,在端粒复制失败后,会出现大规模的缺失、复制不足的 DNA、易位和融合事件。此外,允许进入有丝分裂的复制不足的 DNA 和端粒融合将产生有丝分裂 DNA 桥——这是遗传丢失和染色体重排的已知驱动因素。因此,异常的端粒复制会促进基因组不稳定,进而导致细胞死亡、衰老或致癌转化。这些问题对生物体的健康至关重要,因此需要坚决维护端粒。在这里,我们描述了在识别和理解人类细胞中存在的分子机制方面的最新进展,这些机制可以引导复制体穿过端粒的复杂结构和重复序列。最后,我们回顾了对抗端粒复制叉崩溃时发生的有害后果的途径。