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. 2021 Sep 6;102(9):001647. doi: 10.1099/jgv.0.001647

Table 1.

Primers used during the construction of full-length YFV/RBV chimeric DNAs

Primer

Polarity

Sequence*

Genomic location†

YR1-F

Sense

5′ GAATAAGGGCGACACGGAAATGTC 3′

–

YR1-R

Antisense

5′ CACACAGGATTTACTCGGTTCACTAAACGAG 3′

1–13

YR2-F

Sense

5′ GTTTAGTGAACCGAGTAAATCCTGTGTGC 3′

1–16

YR2-R

Antisense

5′ CATAGCCATCAATCCACCCGTCATCAACAGC 3′

463–493

YR3-F

Sense

5′ CGGGTGGATTGATGGCTATGCAGGTATCCC 3′

474–503

YR3-R

Antisense

5′ GCATCCTTGATCTCCCATGACTCCAGTTGTAAATC 3′

2406–2440

YR4-F

Sense

5′ GAGTCATGGGAGATCAAGGATGCGCCATCAACTTTGG 3′

2418–2454

YR4-R

Antisense

5′ CTGTTATTGAATTCCAGCCACTGACC 3′

7153–7178

YR5-F

Sense

5′ GGTCAGTGGCTGGAATTCAATAACAG 3′

7153–7178

YR5-R

Antisense

5′ TGCCGGCCAGAGGTTTTGTGT 3′

10,829–10,838

YR6-F

Sense

5′ CAAAACCTCTAGCCGGCATGGTC 3′

10,826–10,838

YR6-R

Antisense

5′ GCTGCGCAACTGTTGGGAAG 3′

–

*Sequences are colour-coded: cytomegalovirus promoter, blue; yellow fever virus, black; Rio Bravo virus, red; hepatitis delta virus anti-genomic ribozyme sequence and simian virus 40 polyadenylation signal, green

†Location of the primer binding sites in the chimeric flavivirus genome with numbers starting at the first nucleotide of the flavivirus 5′ untranslated region (not the first nucleotide of the promoter sequence).