Table 3.
Amplification success prediction for the 28 fastest Shaw et al. (2014) regions.a
Approx. Nicotiana order | Basal dicot grade/Magnoliids | Monocots | Basal eudicot grade | Eurosids I | Eurosids II | Euasterids I | Euasterids II | ||||||||
Genomic region | Publicationb | Amborella | Magnolia | Acorus | Cymbidium | Oryza | Canna | Ceratophyllum | Nelumbo | Fragaria | Gossypium | Olea | Helianthus | Average | |
1 | trnH-psbA IGS | 8c | |||||||||||||
trnH-psbA IGS | Dong et al. | NO** | NO** | NO | NO** | NO | NO | NO | NO** | NO | NO | NO | NO** | 0% | |
trnH-psbA IGS | Scarcelli et al. | YES | YES | YES | YES | YES | NO | YES | NO | YES | YES | YES | YES | 83% | |
trnH-psbA IGS | Shaw et al. | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | YES | YES | 92% | |
5 | matK exon | 12c | 6c | 12c | |||||||||||
trnK (including matK) | Dong et al. | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | YES | YES | 92% | |
matK exon | Scarcelli et al. | YES | YES | YES | YES* | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
7 | trnK-rps16 IGS | 13c | 5c | 13c | 7c | 12c | |||||||||
trnK-rps16 | Scarcelli et al. | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | YES | YES* | 92% | |
trnK-3′rpS16 | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
8 | rps16 intron | 4c | 3c | 5c | |||||||||||
rps16 intron | Scarcelli et al. | YES | YES | YES | YES | YES | YES | NO | YES | NO | YES | YES | YES | 83% | |
rpS16 intron | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
9 | rps16-trnQ IGS | 2c | 11c | 1c | 13c | ||||||||||
rps16-trnQ | Dong et al. | YES | YES | YES | YES | NO | NO | YES | YES | NO | NO | NO | YES | 58% | |
rps16-trnQ | Scarcelli et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
5′rpS16-trnQ | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
12 | trnS-trnG IGS | 11c | 2c | 12c | |||||||||||
trnS-trnG (and intron) | Dong et al. | NO | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | NO | 75% | |
trnS-trnG | Scarcelli et al. | NO | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | NO | 75% | |
trnS-trnG | Shaw et al. | YES | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | NO | 83% | |
16 | atpF intron | 5c | |||||||||||||
atpF intron | Prince (here) | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
atpF intron/exon | Scarcelli et al. | NO | YES | YES | NO | YES | YES | NO | YES | NO | YES | YES | YES | 67% | |
18 | atpH-atp IGS | 9c | 12c | 4c | |||||||||||
atpH-atpI | Dong et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | YES | 92% | |
atpH-atpI | Prince (here) | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
atpH-atpI | Scarcelli et al. | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | YES | YES | 92% | |
atpH-atpI | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
26 | rpoB-trnC IGS | 8c | 10c | 11c | 7c | ||||||||||
rpoB-trnC | Dong et al. | YES | YES | YES | NO | NO | NO | YES | YES | YES | YES | YES | NO | 67% | |
rpoB-trnC | Scarcelli et al. | NO | YES | YES | YES | YES | YES | NO | YES | YES | YES | YES | NO | 75% | |
rpoB-trnC | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | NO | 83% | |
29–31 | petN-psbM IGS | 6c | 10c | ||||||||||||
petN-trnD | Scarcelli et al. | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | YES | NO | 83% | |
petN-psbM | Dong et al. | NO | NO | NO | NO | NO | NO | NO | NO | NO | NO | YES | YES | 17% | |
ycf6-psbM | Shaw et al. | YES | YES | YES | NO | YES | NO | YES | YES | YES | YES | NO | YES | 75% | |
32 | psbM-trnD IGS | 8c | 3c | 9c | |||||||||||
psbM-trnD | Dong et al. | YES | YES | YES | NO | NO | YES | YES | YES | YES | YES | YES | YES | 83% | |
psbM-trnD | Shaw et al. | NO | NO | YES | NO | YES | YES | YES | YES | YES | YES | YES | NO | 67% | |
33 | trnE-trnT IGS | 8c | 6c | ||||||||||||
trnD-trnT | Scarcelli et al. | YES | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | NO | 83% | |
trnD-trnT | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | NO | 92% | |
34 | trnT-psbD IGS | 4c | 8c | 4c | 8c | ||||||||||
trnT-psbD | Dong et al. | NO | YES | YES | YES | NO | YES | YES | YES | NO | YES | YES | NO | 67% | |
trnT-psbD | Scarcelli et al. | NO | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | YES | 83% | |
trnT-psbD | Shaw et al. | YES | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | YES | 92% | |
38–41 | psbZ-trnG IGS | 7c | 2c | ||||||||||||
trnS-trnG | Dong et al. | YES | YES | YES | YES | NO | YES | YES | YES | YES | YES | NO | YES | 83% | |
trnS-trnfM | Shaw et al. | YES | YES | NO | YES | YES | YES | YES | NO | YES | NO | NO | YES | 67% | |
psbZ-trnfM | Scarcelli et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
50 | trnT-trnL IGS | 11c | 9c | 3c | |||||||||||
trnT-trnL | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
55 | ndhC-trnV IGS | 5c | 2c | 3c | 3c | ||||||||||
ndhC-trnV | Dong et al. | YES | YES | YES | YES* | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
ndhC-trnV | Prince (here) | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | YES | YES | 92% | |
ndhC-trnV | Scarcelli et al. | YES | YES | YES | YES* | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
ndhC-trnV | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | YES | YES | 92% | |
60 | atpB-rbcL IGS | 9c | |||||||||||||
atpB-rbcL | Prince (here) | YES | YES | YES | NO | YES | YES | YES | YES | NO | NO | YES | YES | 75% | |
atpB-rbcL | Scarcelli et al. | NO | YES | YES | NO | YES | YES | YES | YES* | NO | YES | YES | NO | 67% | |
62 | rbcL-accD IGS | 12c | 13c | ||||||||||||
rbcL-accD | Dong et al. | NO | YES | YES | YES | NO | YES | YES | YES | YES | YES | YES | NO | 75% | |
rbcL-accD | Prince (here) | YES | YES | NO | YES | NO | NO | YES | NO | NO | YES | NO | NO | 42% | |
rbcL-accD | Scarcelli et al. | NO | NO | NO | NO | NO | YES | NO | NO | NO | NO | NO | NO | 8% | |
64 | accD-psaI IGS | 10c | 10c | ||||||||||||
accD-psaI | Dong et al. | NO | YES | NO | NO | NO | YES | YES | YES | YES | YES | YES | YES | 67% | |
accD-psaI | Prince (here) | NO | YES | NO | YES | NO | YES | YES | YES | YES | YES | YES | NO | 67% | |
accD-psaI | Scarcelli et al. | NO | YES | NO | YES | NO | YES | NO | YES | NO | YES | YES | YES | 58% | |
accD-psaI | Shaw et al. | YES | YES | NO | YES | NO | NO | YES | YES | YES | YES | YES | YES | 75% | |
67 | ycf4-cemA (ycf10) IGS | 11c | |||||||||||||
ycf4-ycf10 | Prince (here) | YES | YES | YES | YES | YES | NO | NO | YES | NO | YES | YES | YES | 75% | |
70 | petA-psbJ IGS | 6c | 6c | 5c | 5c | ||||||||||
petA-psbJ | Dong et al. | YES | YES | YES | NO | NO | YES | YES | YES | YES | YES | YES | NO | 75% | |
petA-psbJ | Prince (here) | YES | YES | YES | NO | YES | NO | YES | YES | YES | NO | NO | YES | 67% | |
petA-psbJ | Shaw et al. | YES | YES | YES | NO | YES | YES | YES | YES | NO | NO | YES | YES | 75% | |
72 | psbE-petL IGS | 7c | 7c | 4c | 13c | 9c | |||||||||
psbE-petL | Dong et al. | NO | NO | NO | YES* | NO | YES | YES | NO | YES | NO | YES | YES | 50% | |
psbE-petL | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
76, 77 | psaJ-rpl33 IGS | 13c | |||||||||||||
trnP-rps18 | Scarcelli et al. | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | YES | NO | 92% | |
psaJ-rpL20 | Prince (here) | NO | YES | NO | NO | NO | YES | YES | YES | NO | YES | YES | YES | 58% | |
116 | ndhF-rpl32 IGS | 3c | 1c | 1c | 9c | 2c | |||||||||
ndhF-rpl32 | Scarcelli et al. | YES | YES | YES | YES | YES | NO | YES | YES | YES | NO | YES | YES | 83% | |
ndhF-rpl32 | Shaw et al. | NO | YES | YES | YES | NO | NO | NO | YES | YES | YES | YES | YES | 67% | |
118 | rpl32-trnL IGS | 1c | 6c | 2c | 1c | ||||||||||
rpL32-trnL | Dong et al. | NO | YES | YES | NO | YES | YES | YES | YES | YES | YES | YES | YES | 83% | |
rpL32-trnL | Shaw et al. | YES | YES | YES | YES | YES | YES | YES | YES | NO | YES | YES | YES | 92% | |
121.5 | ndhD-psaC IGS | 10c | |||||||||||||
127 | ndhA intron | 1c | 10c | 11c | |||||||||||
ndhA intron | Dong et al. | NO | NO | NO | YES* | YES | NO | NO | NO | NO | YES | NO | NO | 25% | |
ndhA intron | Scarcelli et al. | YES | YES | YES | YES* | YES | YES | YES | YES | YES | YES | YES | YES | 100% | |
ndhA intron | Shaw et al. | YES | YES | YES | YES* | NO | YES | YES | YES | YES | YES | YES | YES | 92% | |
129 | rps15-ycf1 IGS | 7c | 4c | ||||||||||||
rpS15-ycf1 | Prince (here) | YES | YES | YES | NO | NO | YES | YES | YES | YES | YES | YES | YES | 83% | |
rps15-ycf1 | Scarcelli et al. | YES | NO | YES | YES | NO | YES | YES | NO | YES | YES | NO | YES | 67% |
YES* = will not work for at least one species in the genus; NO** = will work if psbA primer is synthesized with one fewer A at the 3′ end.
Shaw et al. (2014) rank for the region within the specified taxonomic group.