Genome-wide analysis of replication timing by next-generation sequencing with E/L Repli-seq
Nature Protocols • 2018
Publication Information
Authors
Claire Marchal1,4, Takayo Sasaki1,4, Daniel Vera2 , Korey Wilson1, Jiao Sima1, Juan Carlos Rivera-Mulia1,Claudia Trevilla-García1, Coralin Nogues1, Ebtesam Nafie3 & David M Gilbert1,2
Keywords
DNA replicationGenome informaticsGenomic analysisNext-generation sequencing
Journal
Nature Protocols
Publisher
Springer Nature
Volume
13
Issue
2018
Pages
819–839
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
Cycling cells duplicate their DNA content during S phase, following a defined program called replication timing (RT). Early- and
late-replicating regions differ in terms of mutation rates, transcriptional activity, chromatin marks and subnuclear position.
Moreover, RT is regulated during development and is altered in diseases. Here, we describe E/L Repli-seq, an extension of our
Repli-chip protocol. E/L Repli-seq is a rapid, robust and relatively inexpensive protocol for analyzing RT by next-generation
sequencing (NGS), allowing genome-wide assessment of how cellular processes are linked to RT. Briefly, cells are pulse-labeled
with BrdU, and early and late S-phase fractions are sorted by flow cytometry. Labeled nascent DNA is immunoprecipitated from
both fractions and sequenced. Data processing leads to a single bedGraph file containing the ratio of nascent DNA from early
versus late S-phase fractions. The results are comparable to those of Repli-chip, with the additional benefits of genome-wide
sequence information and an increased dynamic range. We also provide computational pipelines for downstream analyses,
for parsing phased genomes using single-nucleotide polymorphisms (SNPs) to analyze RT allelic asynchrony, and for direct
comparison to Repli-chip data. This protocol can be performed in up to 3 d before sequencing, and requires basic cellular and
molecular biology skills, as well as a basic understanding of Unix and R.
late-replicating regions differ in terms of mutation rates, transcriptional activity, chromatin marks and subnuclear position.
Moreover, RT is regulated during development and is altered in diseases. Here, we describe E/L Repli-seq, an extension of our
Repli-chip protocol. E/L Repli-seq is a rapid, robust and relatively inexpensive protocol for analyzing RT by next-generation
sequencing (NGS), allowing genome-wide assessment of how cellular processes are linked to RT. Briefly, cells are pulse-labeled
with BrdU, and early and late S-phase fractions are sorted by flow cytometry. Labeled nascent DNA is immunoprecipitated from
both fractions and sequenced. Data processing leads to a single bedGraph file containing the ratio of nascent DNA from early
versus late S-phase fractions. The results are comparable to those of Repli-chip, with the additional benefits of genome-wide
sequence information and an increased dynamic range. We also provide computational pipelines for downstream analyses,
for parsing phased genomes using single-nucleotide polymorphisms (SNPs) to analyze RT allelic asynchrony, and for direct
comparison to Repli-chip data. This protocol can be performed in up to 3 d before sequencing, and requires basic cellular and
molecular biology skills, as well as a basic understanding of Unix and R.
Staff Members - Benha University