Table 1.
Cultivar or line | Vernalization and photoperiod genes | ||||
VRNH1a | VRNH2b | VRNH3c | PPDH1d | PPDH2e | |
‘Plaisant’ | vrnh1 | VRNH2 | vrnH3 | PPDH1 | ppdH2 |
SBCC106 | VRNH1-6 | VRNH2 | vrnH3 | PPDH1 | PPDH2 |
SBCC058 | VRNH1-4 | VRNH2 | vrnH3 | PPDH1 | PPDH2 |
‘Alexis’ | VRNH1-3 | vrnH2 | vrnH3 | ppdH1 | PPDH2 |
‘Pané’ | VRNH1-4 | VRNH2 | vrnH3 | PPDH1 | PPDH2 |
‘Beka’ | VRNH1-1 | vrnH2 | vrnH3 | ppdH1 | PPDH2 |
‘Mogador’ | vrnh1 | VRNH2 | vrnH3 | ppdH1 | ppdH2 |
Alleles based on the size of intron 1, in accordance with Hemming et al. (2009).
Presence/absence of HvZCCT, in accordance with Karsai et al. (2005).
Alleles based on two SNPs in intron 1, as reported by Yan et al. (2006).
Alleles based on SNP22 of Turner et al. (2005).
Alleles based on amplification of a 431 bp product using primers FT3.1F (5'-ATCCATTGGTTGTGTGGCTCA-3') and FT3.2R (5'-ATCTGTCACCAACCTGCACA-3'), which amplify the entire region from exons 1 to 2 of the HvFT3 gene (‘Alexis’, SBCC058, SBCC106, ‘Pané’, and ‘Beka’). These primers give a null allele for ‘Plaisant’ and ‘Mogador’. The allele from ‘Plaisant’ (ppdH2) was amplified using the F4/R1 primers reported by Kikuchi et al. (2009). HvFT3 was localized on the long arm of chromosome 1H in the ‘Beka’בMogador’ mapping population (Supplementary Fig. S1 at JXB online), which matches the location of a QTL for response to a short photoperiod (Supplementary Fig. S2).