Identification of candidate genes associated with mealiness and maturity date in peach [Prunus persica (L.) Batsch] using QTL analysis and deep sequencing

被引:63
作者
Nunez-Lillo, Gerardo [1 ]
Cifuentes-Esquivel, Alejandra [1 ,2 ]
Troggio, Michela [3 ]
Micheletti, D. [3 ]
Infante, Rodrigo [2 ]
Campos-Vargas, Reinaldo [1 ]
Orellana, Ariel [1 ,4 ]
Blanco-Herrera, Francisca [1 ]
Meneses, Claudio [1 ]
机构
[1] Univ Andres Bello, Ctr Biotecnol Vegetal, Santiago, Chile
[2] Univ Chile, Dept Prod Agr, Santiago, Chile
[3] Fdn Edmund Mach, Res & Innovat Ctr, San Michele All Adige, TN, Italy
[4] Univ Andres Bello, FONDAP Ctr Genome Regulat, Fac Ciencias Biol, Santiago, Chile
关键词
Genetic linkage map; Slow ripening; ANAC072; ERF4; CONTROLLED-ATMOSPHERE STORAGE; MARKER-ASSISTED SELECTION; NAC TRANSCRIPTION FACTORS; CONTROLLING FRUIT-QUALITY; LINKAGE MAP; POSTHARVEST PHYSIOLOGY; RIPENING MUTANTS; CHILLING INJURY; TOMATO; ETHYLENE;
D O I
10.1007/s11295-015-0911-9
中图分类号
S7 [林业];
学科分类号
0829 ; 0907 ;
摘要
Peach and nectarine quality traits such as flavor, texture, and juiciness are important for consumer acceptance. Maturity date (MD) also plays a role in the fruit-ripening process and is an important factor for marketing fresh fruit. On the other hand, cold storage produces a physiological disorder known as chilling injury where the most important symptom is a lack of juice in the flesh or mealiness (M). In this study, we analyzed an F2 population obtained from a self-pollination of "Venus" nectarine that segregates for MD and M. We built a linkage map with 1,830 SNPs, 7 SSRs and two slow-ripening (SR) morphological markers, spanning 389.2 cM distributed over eight linkage groups (LGs). The SR trait was mapped to LG4 and we compared the whole genome sequences of a SR individual and "Venus" and identified a deletion of 26.6 kb containing ppa008301m (ANAC072) co-localized with the SR trait. Three Quantitative Trait Loci (QTL) for MD were detected; they all co-localize on LG4 between 31.0 and 42.0 cM. Four co-localizing QTLs on LG4 between 33.3 and 40.3 cM were detected for M, explaining 34 % of the phenotypic variation. We identified five and nine candidate genes (CGs) for MD and M from the QTL regions, respectively. Our results suggest that the transcription factors (TFs) ANAC072 and ppa010982m (ERF4) are CGs for both traits. LG4 contains a cluster for genetic factors that possibly regulate MandMD, but functional validation is necessary to unravel the complexity of genetic control responsible for fruit traits.
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页数:13
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