SUMMARY
Peach (Prunus persica L. Batsch) is an economically important fruit crop worldwide. Although a high‐quality peach genome has previously been published, Sanger sequencing was used for its assembly, which generated short contigs. Here, we report a chromosome‐level genome assembly and sequence analysis of Chinese Cling, an important founder cultivar for peach breeding programs worldwide. The assembled genome contained 247.33 Mb with a contig N50 of 4.13 Mb and a scaffold N50 of 29.68 Mb, representing 99.8% of the estimated genome. Comparisons between this genome and the recently published one (Lovell peach) uncovered 685 407 single nucleotide polymorphisms, 162 655 insertions and deletions, and 16 248 structural variants. Gene family analysis highlighted the contraction of the gene families involved in flavone, flavonol, flavonoid, and monoterpenoid biosynthesis. Subsequently, the volatile compounds of 256 peach varieties were quantitated in mature fruits in 2015 and 2016 to perform a genome‐wide association analysis. A comparison with the identified domestication genomic regions allowed us to identify 25 quantitative trait loci, associated with seven volatile compounds, in the domestication region, which is consistent with the differences in volatile compounds between wild and cultivated peaches. Finally, a gene encoding terpene synthase, located within a previously reported quantitative trait loci region, was identified to be associated with linalool synthesis. Such findings highlight the importance of this new assembly for the analysis of evolutionary mechanisms and gene identification in peach species. Furthermore, this high‐quality peach genome provides valuable information for future fruit improvement.
Blooming in temperate fruit species is triggered by chilling and heat requirements (CR and HR), with a wide range of requirements within the same species. CR for flower bud dormancy release has become a limiting factor for geographical adaptation of fruit trees in warmer regions. The present study investigated the genetic basis of CR and HR to break dormancy and flowering time (FT) in an almond x peach F2 progeny. FT, HR and CR were evaluated over two consecutive years (2015/2016 and 2016/2017). Seven out of the eight identified quantitative trait loci (QTLs) were found in both periods of analysis. They affected eight traits, and included a consistent QTL for breaking dormancy, CR and HR. Two of them, affecting FT and HR for FT (GDHF), colocalized in G1, and the remaining QTLs, affecting chilling and heat requirements, both influenced by dormancy breaking (DB), were located in G6. These results indicate that factors not related to DB affect flowering time in this population. Implications of the results in peach breeding are discussed.
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