Rapid profiling of DNA replication dynamics using mass spectrometry-based analysis of nascent DNA

The primary method for probing DNA replication dynamics is DNA fiber analysis, which utilizes thymidine analog incorporation into nascent DNA, followed by immunofluorescent microscopy of DNA fibers. Besides being time-consuming and prone to experimenter bias, it is not suitable for studying DNA replication dynamics in mitochondria or bacteria, nor is it adaptable for higher-throughput analysis. Here, we present mass spectrometry-based analysis of nascent DNA (MS-BAND) as a rapid, unbiased, quantitative alternative to DNA fiber analysis. In this method, incorporation of thymidine analogs is quantified from DNA using triple quadrupole tandem mass spectrometry. MS-BAND accurately detects DNA replication alterations in both the nucleus and mitochondria of human cells, as well as bacteria. The high-throughput capability of MS-BAND captured replication alterations in an E. coli DNA damage-inducing gene library. Therefore, MS-BAND may serve as an alternative to the DNA fiber technique, with potential for high-throughput analysis of replication dynamics in diverse model systems. Ashour et al. present a mass spectrometry-based tool to assay DNA replication. The technique, termed mass-spectrometry-based analysis of nascent DNA (MS-BAND), permits quantitation of replication in human and bacterial cells, as well as mitochondria. MS-BAND can perform higher-throughput replication analysis, which may prove advantageous compared to established methods.

Automated summary

The primary method for studying DNA replication dynamics, DNA fiber analysis, has limitations in terms of time, bias, and adaptability. In this study, a mass spectrometry-based analysis technique (MS-BAND) was introduced as a rapid and unbiased alternative for quantifying and analyzing DNA replication. MS-BAND accurately detects replication alterations in various cell compartments and has high-throughput capability, making it a potential alternative to the DNA fiber technique.