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*Contributed equally to this work Published: Vol 9, Iss 15, Aug 5, 2019 DOI: 10.21769/BioProtoc.3329 Views: 6942
Edited by: Elizabeth Libby Reviewed by: Michael TschernerTimo A Lehti
Abstract
Most bacterial genomes have biased nucleotide composition, and the asymmetry is considered to be caused by a single-stranded DNA (ssDNA) deamination arising from the bacterial replication machinery. In order to evaluate the relationship experimentally, the position and frequency of ssDNA formed during replication must be verified clearly. Although many ssDNA detection technologies exist, almost all methods have been developed for eukaryotic genomes. To apply these to bacterial genomes, which harbor a smaller amount of DNA than those of eukaryotes, more efficient, new methods are required. Therefore, we developed a novel strand-specific ssDNA sequencing method, called 4S-seq, for the bacterial genome. The 4S-seq method enriches ssDNA in the extracted genomic DNA by a dsDNA-specific nuclease and implements a strand-specific library using a biotin label with a customized tag. As a result, the 4S-seq is able to calculate the ssDNA content in each strand (Watson/Crick) at each position of the genome efficiently.
Keywords: Bacterial genomeBackground
Nascent and template strand tracking is an important approach to investigate bacterial genome evolution. Since biased mutations in bacterial genome arise from asymmetric replication machinery, DNA strands that have been exposed to a single-stranded state for a long time will accumulate more mutations. Several strand-specific sequencing technologies are available for eukaryotic genomes, with various selection strategies for nascent DNA (Hyrien, 2015). In general, the nascent DNA is caught by immunoprecipitation with BrdU (Karnani et al., 2010) or a combination of antibodies against strand-specific binding proteins (Yu et al., 2014). Other protocols utilize a customized label (Smith and Whitehouse, 2012) or an agarose gel trap (Mesner et al., 2011) to select nascent DNA of a certain size. However, these strand-specific sequencing technologies for eukaryotic genomes are not readily applicable to bacterial genomes because the BrdU incorporation efficiency or the amount of DNA is overwhelmingly low in bacteria. Therefore, we developed a novel 4S-seq method for the bacterial genome. Overall, the 4S-seq method is broadly divided into ssDNA enrichment and strand-specific sequencing steps (Figure 1). The ssDNA is enriched in the fragmented genomic DNA using a duplex-specific nuclease. The strand-specific sequencing is implemented using a biotinylated adapter with an exclusively unique designed tag. At this time, the library is prepared using a low input library preparation kit because a low amount of enriched ssDNA is expected. Sequenced reads are analyzed with a custom Perl script, and the ssDNA location and strand are calculated. The new 4S-seq method for the bacterial genome described here does not require specialized equipment and can be applied from plasmid to mega-scale genomes. This 4S-seq was applied to research investigating the relationship between a base compositional bias in a bacterial genome and a spontaneous mutation in ssDNA, and revealed that there is a strong correlation between ssDNA frequency and the mutation rate (Kono et al., 2018). We show the protocol optimized for Escherichia coli.

Figure 1. Overview of the 4S-seq protocol. Steps A-C: purification of the sheared genomic DNA from E. coli cultures; Steps D-F: preparation of dephosphorylated ssDNA and the phosphorylated adapter; Steps G-J: purification of tagged ssDNA fragments using streptavidin beads; Step K: preparation of the library for the Illumina sequencer.
Materials and Reagents
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Procedure
Category
Microbiology > Microbial genetics > DNA > DNA sequencing
Molecular Biology > DNA > DNA sequencing
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