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. 2021 Apr 12;95(9):e01939-20. doi: 10.1128/JVI.01939-20

TABLE 2.

m6A peaks in Sendai virus RNAs

SeV RNA peak no.a Peak range (nt)b Gene locationc Peak size (nt) Fold enrichmentd Putative m6A site(s)e
1 351–450 N 99 1.34 AGACC
2 1401–1750 N 349 2.63 AAACA, GGACC, AAACC, AGACA, AGACT, AAACT
3 2101–2500 P 399 2.37 GAACA, AAACC, AAACA, GAACT, AAACT, AGACT, AAACA, AGACC, GGACT, GAACT
4 2651–2750 P 99 1.56 GGACA, AGACC, AAACC, GGACC
5 3251–3600 P 349 3.35 AAACC, GGACC, GGACA, GAACC, AGACA, AGACC, GAACT, GGACA
6 5301–5400 GFP 99 1.39 GAACT
a

Total RNA was extracted from rSeV-GFP or mock-infected A549 cells and subjected to sonication. RNA containing m6A methylation was pulled down by m6A antibody. Three replicates (n = 3) of RNA from virus-infected cells were m6A sequenced.

b

Nucleotide sequence position with reference to the Sendai virus Z strain expressing GFP (GenBank accession no. AB855655). Nucleotide ranges are indicated.

c

The SeV genes and GFP gene are covered by m6A peaks. These regions may contain m6A sites.

d

Log2 enrichment of the m6A peaks identified in the SeV antigenome and mRNAs.

e

Putative m6A sites are identified based on searching for the presence of the m6A motif Pu [G > A]m6AC[A/C/U] (where Pu represents purine) in the peak ranges.