Abstract

DNA replication is a stochastic process with replication forks emanating from multiple replication origins. The origins must be licenced in G1, and the replisome activated at licenced origins in order to generate bi-directional replication forks in S-phase. Differential firing times lead to origin interference, where a replication fork from an origin can replicate through and inactivate neighbouring origins (origin obscuring). We developed a Bayesian algorithm to characterize origin firing statistics from Okazaki fragment (OF) sequencing data. Our algorithm infers the distributions of firing times and the licencing probabilities for three consecutive origins. We demonstrate that our algorithm can distinguish partial origin licencing and origin obscuring in OF sequencing data from Saccharomyces cerevisiae and human cell types. We used our method to analyse the decreased origin efficiency under loss of Rat1 activity in S. cerevisiae, demonstrating that both reduced licencing and increased obscuring contribute. Moreover, we show that robust analysis is possible using only local data (across three neighbouring origins), and analysis of the whole chromosome is not required. Our algorithm utilizes an approximate likelihood and a reversible jump sampling technique, a methodology that can be extended to analysis of other mechanistic processes measurable through Next Generation Sequencing data.

Highlights

  • In eukaryotes, replication of DNA is achieved by establishment of multiple bi-directional replication forks at genomic sites called replication origins [1,2]

  • With the emergence of powerful sequencing technologies, it is reasonable to expect that this stochastic process can be parametrized from experimental data, thereby achieving a new level of understanding. This is the question we tackle here: can the stochastic origin replication process incorporating probabilistic origin licencing and variability in origin firing times be inferred from sequencing data? We develop a Bayesian approach to fit the model of Retkute et al [17,18], generating a full parametrization of origin use and firing times from Okazaki fragment (OF) sequencing data

  • We use a Bayesian Markov chain Monte Carlo (MCMC) algorithm to analyse the OF data from two protocols: (i) S. cerevisiae OF sequencing from ligase mutants, where OFs were harvested after 2.5 h of ligase inactivation

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Summary

Introduction

Replication of DNA is achieved by establishment of multiple bi-directional replication forks at genomic sites called replication origins [1,2]. In order to ensure that the genome is replicated once and only once per cell cycle, a two-step process takes place. The pre-replicative complex (Pre-RC), which contains the origin recognition complex and minichromosome maintenance (MCM) helicases is loaded onto origins during G1 phase. This is referred to as origin licencing and is temporally restricted to the G1 phase. It is estimated that many origins are licenced during each G1 phase, and only a fraction (approximately one-fourth) of these licenced origins are activated in S-phase [3,4]

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