a Department of Microbiology and Molecular Genetics , University of California , Davis , CA , USA.
b Department of Biochemistry, Molecular Biology and Biophysics , University of Minnesota Medical School , Minneapolis , MN , USA.
Cell Cycle. 2019 Apr;18(8):880-888. doi: 10.1080/15384101.2019.1598724. Epub 2019 Apr 6.
The double-stranded telomeric binding protein TRF2 is expressed in many human cancers at elevated levels. Moreover, experimental overexpression of TRF2 in human cells causes replication stalling in telomeric tracts, which leads to drastic telomere shortening and fusion of deprotected chromosome ends. To understand which end joining pathway is involved in mediating these chromosome fusions, we overexpressed TRF2 in human HCT116 cell lines that were deficient for the DNA Ligase 4 (Lig4)-dependent classical non-homologous end joining (C-NHEJ) or the DNA Ligase 3 (Lig3)-dependent alternative non-homologous end joining (A-NHEJ) pathway. Surprisingly, abrogation of either Lig4 or nuclear Lig3 significantly reduced inter-chromosomal fusion of drastically shortened telomeres, suggesting that both the C-NHEJ and A-NHEJ pathways are involved in mediating this type of fusion. Fusion between deprotected sister chromatids, however, only required the Lig3-dependent A-NHEJ pathway. Interestingly, a previous study reported similar end joining pathway requirements for the fusion of critically shortened telomeres during a telomere attrition-based cellular crisis. We speculate that, as in cellular crisis, the same repair pathway(s) may drive clonal and genomic evolution in human cancers containing elevated TRF2 levels.
端粒结合蛋白 TRF2 在许多人类癌症中呈高水平表达。此外,在人类细胞中过表达 TRF2 会导致端粒区的复制停滞,从而导致端粒急剧缩短和去保护的染色体末端融合。为了了解哪种末端连接途径参与介导这些染色体融合,我们在人 HCT116 细胞系中过表达 TRF2,这些细胞系缺乏 DNA 连接酶 4(Lig4)依赖性经典非同源末端连接(C-NHEJ)或 DNA 连接酶 3(Lig3)依赖性替代非同源末端连接(A-NHEJ)途径。令人惊讶的是,敲除 Lig4 或核 Lig3 均显著降低了急剧缩短的端粒之间的染色体间融合,表明 C-NHEJ 和 A-NHEJ 途径均参与介导这种类型的融合。然而,去保护的姐妹染色单体之间的融合仅需要 Lig3 依赖性 A-NHEJ 途径。有趣的是,先前的一项研究报告称,在基于端粒损耗的细胞危机期间,临界缩短的端粒融合需要类似的末端连接途径。我们推测,与细胞危机一样,在含有高水平 TRF2 的人类癌症中,相同的修复途径(或途径)可能驱动克隆和基因组进化。