Determining S- genotypes of two sweet cherry (Prunus avium L.) cultivars, 'Takasago (Rockport Bigarreau)' and 'Hinode (Early Purple)'

Citation
H. Yamane et al., Determining S- genotypes of two sweet cherry (Prunus avium L.) cultivars, 'Takasago (Rockport Bigarreau)' and 'Hinode (Early Purple)', J JPN S HOR, 69(1), 2000, pp. 29-34
Citations number
24
Categorie Soggetti
Plant Sciences
Journal title
JOURNAL OF THE JAPANESE SOCIETY FOR HORTICULTURAL SCIENCE
ISSN journal
00137626 → ACNP
Volume
69
Issue
1
Year of publication
2000
Pages
29 - 34
Database
ISI
SICI code
0013-7626(200001)69:1<29:DSGOTS>2.0.ZU;2-Q
Abstract
'Takasago (Rockport Bigarreau)', one of the major early ripening cultivars of sweet cherry in Japan, was reported to be cross-incompatible with 'Hinod e (Early Purple)'. Thus, they were assumed to have the same S- alleles, alt hough their S-genotypes were unknown. However, when 'Takasago' was cross-po llinated with 'Hinode' at the Yamagata Prefectural Horticultural Experiment Station, the fruit set normally (unpublished data), which suggests that th ey are cross-compatible. In this study, we re-evaluated crossability betwee n the two cultivars by controlled pollination tests and determined their S- genotypes by the molecular typing system recently developed for S-alleles o f sweet cherry. The cross-pollination tests conducted at two different loca tions in Japan showed that 'Takasago' and 'Hinode' were self- incompatible but reciprocally cross- compatible. Furthermore, 2D-PAGE (two dimentional- polyacrylamide gel electrophoresis) analysis for stylar extracts revealed t hat they have none of the common S-RNases, S-gene products in styles of swe et cherry, which suggests that their S-genotypes are completely different. By S-RNase spot patterns in 2D-PAGE profiles and RFLP (restriction fragment length polymorphism) analysis, S-genotypes of 'Takasago' and 'Hinode' were proposed to be S-1 S-6 and S S-2(x) (S-x is a novel S-allele different fro m S-1 to S-6), respectively. This implies that 'Hinode' is cross- compatibl e with all cultivars of known S-genotypes. The usefulness of biochemical an d molecular methods for S- allele typing employed in this study is discusse d.