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Transcriptome Analysis of Peach Fruits at Different Developmental Stages in Peach Kurakato Wase and Early-ripening Mutant

PENG JiaWei1, ZHANG YE3, KOU DanDan4, YANG LI1, LIU XiaoFei1, ZHANG XueYing1*, CHEN HaiJiang1*, TIAN YI2* #br#   

  1. 1Horticultural Department, Agricultural University of Hebei, Baoding 071000, Hebei; 2Mountainous Areas Research Institute, Technology Innovation Center for Agriculture in Mountainous Areas of Hebei Province, National Engineering Research Center for Agriculture in Northern Mountainous Areas, Hebei Agricultural University, Baoding 071001, Hebei; 3Baoding Municipal Bureau of Agriculure ang Rural Affairs, Baoding 071000, Hebei; 4Wangshu town Middle School of Yanshan County, Hebei Province, Cangzhou 061300, Hebei
  • Published:2022-08-21

Abstract: ObjectiveIn this study, transcriptome analyses were carried out on the fruits of Kurakato Wase peach and its early-ripening mutant at different developmental stages. The key factors involved in fruit ripening regulation were explored, which provided a theoretical basis for further study on the regulation mechanism of fruit ripening. MethodThe flesh of Kurakato Wase peach and its early-ripening mutant was sampled at 30 d, 45 d, 59 d, 71 d and 89 d after anthesis, and transcriptome analyses were performed on the above samples. The candidate differentially expressed genes (DEGs) were verified by quantitative real-time PCR (qRT-PCR). The biological function of DEGs were analyzed through GO function and KEGG pathway. The weighted gene co-expression network analysis (WGCNA) was constructed to identify the hub modules and hub genes closely related to fruit ripening. ResultFour comparison groups including y1 vs c1, y2 vs c2, y3 vs c4 and y4 vs c5 were obtained based fruit development stagesA tatal of 4 395 DEGs were identified with 2 212 up- and 2 183 down-regulated genes. There are 10, 11 and 18 candidate genes involved in ethylene, abscisic acid and auxin synthesis and signal transduction, respectively. We also constructed the interaction networks between 10 IAA proteins and their predictive interacting proteins ARF. GO function revealed that the DEGs were mainly enriched in cellular processes, metabolic processes and monomeric processes in the biological process category; in cell component category, DEGs were mainly enriched in membranes and cellular components; in molecular function category, DEGs were mainly enriched in binding protein and catalytic activity. There are more DEGs in comparison groups y3 vs c4 and y4 vs c5, and these DEGs mainly enriched in molecular functions such as binding and catalytic activity. The KEGG pathway analysis showed that a variety of secondary metabolites changed during fruit development and ripening, such as sesquiterpene and triterpenoid biosynthesis, flavonoid biosynthesis, carotenoid biosynthesis and α-linolenic acid metabolism. In addition, auxin signal transduction pathway was found to be enriched at different time nodes. ConclusionAmong DEGs, a large number of hormone signal transduction pathway genes, especially auxin signal pathway genes, were enriched, and these genes may play an extremely important role during fruit ripening. The functions of candidate genes IAA and ARF and the molecular regulation of fruit ripening will be further elucidated in the future studies.


Key words: peach, fruit ripening, RNA-seq, WGCNA

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