Skip to main content
. 2020 Jun 16;94(13):e00205-20. doi: 10.1128/JVI.00205-20

TABLE 2.

Schematic presentation of the coding regions of RNase L, G3BP1, RIG-I, PKR, and RIG-I/PKR dKO that are targeted by CRISPR-Cas9

Gene Sequence typea Sequenceb
RNase L REF ATGGGGCCACGCCTTTTATCCTCGCAGCGATTGCGGGG AGCGTGAAGCTGCTGAAACTTTTCCT
MUT ATGGGGCCACGCCTTTTATCCTC ----------------------- GCTGCTGAAACTTTTCCT
G3BP1 REF GGTTGAATTGACCAAAGCAATGGTGATGGAGAAGCCTAGTCCCCTGCTGGTCGGGCGGGAAT TTGTGA
MUT GGTTGAATT ------------------------------------------------- GAATTTGTGA
RIG-I REF TTCCAGGATTATATCCGGAAG-* ACCCTGG ACCCTACCTACA
MUT TTCCAGGATTATATCCGGAAGAACCCTGGACCCTACCTACA
PKR REF CTAATTCAGGACCTCCACATGA-* TAGGAGG TAGGTTGC
MUT CTAATTCAGGACCTCCACATGATTAGGAGGTAGGTTGC
RIG-I/PKR dKOc REF TTCCAGGATTATATCCGGAAG-* ACCCTGG ACCCTACCTACA
MUT TTCCAGGATTATATCCGGAAGAACCCTGGACCCTACCTACA
REF CTAATTCAGGACCTCCACATGA-* TAGGAGG TAGGTTGC
MUT CTAATTCAGGACCTCCACATGATTAGGAGGTAGGTTGC
a

REF, reference sequence; MUT, mutated sequence.

b

The reference sequence and the mutated sequence for each gene are shown, as confirmed by sequencing. The boldface letters denote the protospacer (sgRNA-binding site); the underlined letters indicate the PAM (protospacer-adjacent motif).

c

The top two sequences are RIG-I; the bottom two sequences are PKR.