Fruit development period (FDP), defined as the time between full bloom and maturity, varies greatly in peaches (Prunus persica L. Batsch). It is necessary to develop molecular markers associated with maturity date to extend the harvest season in new peach cultivars. We designed the 260 SSR primer set covering the entire genome of approximately 300 kb to 1 Mb based on P. persica cultivar ‘Mihong’ genome sequence. The SSR markers were used to survey the relationship between the parentages ‘Yumeyong’ and ‘Chiyomaru’ and their offspring cultivars ‘Mihong’, ‘Yumi’, ‘Misshong’ and ‘Soomee’. Male cultivar ‘Chiyomaru and its offspring cultivars ‘Mihong’, Yumi’, and ‘Misshong’ are early and middle maturity cultivars with FDP of 77, 76, 82, and 108 days, respectively, whereas female cultivar ‘Yumyeong’ and its offspring cultivar ‘Soomee’ are late maturity cultivars with FDP of 128 days. Three regions of SSR markers could distinguish between early, middle, and late maturity cultivars. In the early stages of breeding, these markers will be used for marker-assisted selection (MAS) in the parentages ‘Yumyeong’ and ‘Chiyomaru’ and their offspring cultivars.

Prunus persica “Mihong” cultivar is a domesticated white peach that was generated from the crossing between “Yumyeong” and “Chiyomaru” cultivars in the Republic of Korea in 1995. We launched “Mihong” genome sequencing in 2018 and “Mihong” reached to 200 scaffold and 241 Mb sequences using long-read sequencing and Hi-C technology. F₁ populations of ”Kawanakajima Hakuto,” “Mihong,” “Changhowon Hwangdo,” and “Yumi” were developed in NIHHS. These four cultivars were sequenced and assembled using the SOAPdenovo version 2.04. First, we surveyed the SSRs in “Mihong” assembly sequences and extracted the ±300 bp flanking sequences containing SSRs. Second, the assembly sequences of three cultivars were aligned and mapped against “Mihong” ±300 bp flanking sequences using BLASTn (version 2.2.29+). We anticipated the differential length in SSRs among the four cultivars. We sorted the primers with a standard deviation over 4.5 (STEV > 4.5) among the four cultivars. In addition, we surveyed the primers having difference in over 10 bp with “Kawanakajima Hakuto” and “Mihong” for polymorphic markers in the mapping population. All primer pairs were designed to generate amplicons of 150-200 bp in coating SSR regions using primer3 (version 3-2.2.3). We selected 260 SSR markers with a physical distance of average per 1 Mb. These SSR markers accounted for 74% polymorphism in the four genotypes. Finally, a F₁ population of “Kawanakajima Hakuto” and “Mihong” covered 884.5 cM with 465 SNPs and 86 SSRs and this genetic map matched correctly to the HI-C pseudomolecule of P. persica.

In this study, phenotypic distribution of 15 major fruit quality traits were analyzed using 252 progenies derived from a cross between ‘Tano Red’ (seed) and ‘Ruby Seedless’ (seedless), to obtain basic data for improving the breeding efficiency of grapevine cultivars. Berry skin color was dark red-violet in 46.4% of the progenies, which is the color of ‘Tano Red’ and ‘Ruby Seedless’, and berry shape was elliptic in 48.4%. Most of the progenies were very juicy with soft flesh, and closely related to the characteristics of ‘Tano Red’. Seeds were well developed in 67.1% of the progenies, rudimentary in 30.1%, and 2.8% were seedless, with seed weight being less than 0.15 g in 84.9% of the progenies. Among the 15 fruit quality traits assessed, bunch density, ease of berry detachment from pedicel, berry weight, berry seed number, berry longitudinal diameter, berry transverse diameter, berry soluble solids, and berry acidity showed normal distributions. Heritability of berry weight, berry longitudinal diameter, berry transverse diameter, berry soluble solids, and berry acidity was 0.89, 0.82, 0.78, 0.86, and 0.93, respectively. Berry weight was positively correlated with seed weight (r = 0.486^**), presence of seeds (r = 0.483^**), and seed number (r = 0.211^**). Seed weight significantly increased with presence of seeds (r = 0.607^**) and seed number (r = 0.725^**). In addition, presence of seeds was positively correlated with seed number (r = 0.319^**). These results could be useful for the identification of quantitative trait loci associated with fruit quality to assist in grapevine breeding.

Apple (Malus × domestica Borkh.) has gametophytic self-incompatibility (S) controlled by the multi-allelic S-locus. In the present study, S-genotypes of 24 apple cultivars including newly released Korean cultivars and seven crabapple cultivars were identified using S-allele specific polymerase chain reaction analysis. Twelve different S-alleles (S₁, S₂, S₃, S₅, S₇, S₉, S₁₀, S₁₆, S₂₁, S₂₃, S₂₆, and S₂₉) from 31 apple and crabapple cultivars were identified using 23 S-allele specific primers. Among them, S₁ (41.7%), S₃ (58.3%), S₇ (29.2%), and S₉ (54.2%) S-alleles were found to be common in 24 apple cultivars. The newly released Korean cultivars ‘Arisoo’ and ‘Hwangok’ were genetyped as S3S7 and S3S9, respectively. S-genotypes information obtained from the present study will be useful to select proper pollinzers for stable production of apple fruit and to design cross of breeding programs.