Rxivist logo

Mammalian CST averts replication failure by preventing G-quadruplex accumulation

By Yang Liu, Miaomiao Zhang, Bing Wang, Yingnan Xiao, Tingfang Li, X Geng, Guang Li, Qiang Liu, Carolyn M. Price, Feng Wang

Posted 22 Jun 2018
bioRxiv DOI: 10.1101/354050 (published DOI: 10.1093/nar/gkz264)

Human CST (CTC1-STN1-TEN1) is an RPA-like complex that associates with G-rich single-strand DNA and helps resolve replication problems both at telomeres and genome-wide. We previously showed that CST binds and disrupts G-quadruplex (G4) DNA in vitro, suggesting that CST may prevent in vivo blocks to replication by resolving G4 structures. Here, we demonstrate that CST binds and unfolds G4 with similar efficiency to RPA. In cells, CST is recruited to telomeric and non-telomeric chromatin upon G4 stabilization. STN1 depletion increases G4 accumulation and slows bulk genomic DNA replication. At telomeres, combined STN1 depletion and G4 stabilization causes multi-telomere FISH signals and telomere loss, hallmarks of deficient telomere duplex replication. Strand-specific telomere FISH indicates preferential loss of C-strand DNA while analysis of BrdU uptake during leading and lagging-strand telomere replication shows preferential under-replication of lagging telomeres. Together these results indicate a block to Okazaki fragment synthesis. Overall, our findings indicate a novel role for CST in maintaining genome integrity through resolution of G4 structures both ahead of the replication fork and on the lagging strand template.

Download data

  • Downloaded 387 times
  • Download rankings, all-time:
    • Site-wide: 61,743
    • In molecular biology: 1,816
  • Year to date:
    • Site-wide: 74,879
  • Since beginning of last month:
    • Site-wide: 45,845

Altmetric data


Downloads over time

Distribution of downloads per paper, site-wide


PanLingua

Sign up for the Rxivist weekly newsletter! (Click here for more details.)


News