A single QTL harboring multiple genetic variations leads to complicated phenotypic segregation in apple flesh firmness and crispness

• Published in: Plant cell reports 2022-12, Vol.41 (12), p.2379-2391
• Main Authors: Yang, Xianglong, Wu, Bei, Liu, Jing, Zhang, Zhongyan, Wang, Xuan, Zhang, Haie, Ren, Xuejun, Zhang, Xi, Wang, Yi, Wu, Ting, Xu, Xuefeng, Han, Zhenhai, Zhang, Xinzhong
• Format: Article
• Language: English
• Subjects: Alleles; Apples; Biomedical and Life Sciences; Biotechnology; Breeding; Cell Biology; Exons; Firmness; Fruits; Gene expression; Gene mapping; Genes; Genetic diversity; Life Sciences; Nucleotides; Original Article; Phenotypes; Phenotypic variations; Plant Biochemistry; Plant Sciences; Proteins; Quantitative trait loci; Recombination; Single-nucleotide polymorphism
• ISSN: 0721-7714; 1432-203X
• DOI: 10.1007/s00299-022-02929-z

Key Message Within a QTL, the genetic recombination and interactions among five and two functional variations at MdbHLH25 and MdWDR5A caused much complicated phenotype segregation in apple FFR and FCR. The storability of climacteric fruit like apple is a quantitative trait. We previously identified 62 quantitative trait loci (QTLs) associating flesh firmness retainability (FFR) and flesh crispness retainability (FCR), but only a few functional genetic variations were identified and validated. The genetic variation network controlling fruit storability is far to be understood and diagnostic markers are needed for molecular breeding. We previously identified overlapped QTLs F16.1/H16.2 for FFR and FCR using an F1 population derived from ‘Zisai Pearl’ × ‘Red Fuji’. In this study, five and two single-nucleotide polymorphisms (SNPs) were identified on the candidate genes MdbHLH25 and MdWDR5A within the QTL region. The SNP1 A allele at MdbHLH25 promoter reduced the expression and SNP2 T allele and/or SNP4/5 GT alleles at the exons attenuated the function of MdbHLH25 by downregulating the expression of the target genes MdACS1 , which in turn led to a reduction in ethylene production and maintenance of higher flesh crispness. The SNPs did not alter the protein–protein interaction between MdbHLH25 and MdWDR5A . The joint effect of SNP genotype combinations by the SNPs on MdbHLH25 (SNP1, SNP2, and SNP4) and MdWDR5A (SNPi and SNPii) led to a much broad spectrum of phenotypic segregation in FFR and FCR. Together, the dissection of these genetic variations contributes to understanding the complicated effects of a QTL and provides good potential for marker development in molecular breeding.