Biotechnology Bulletin ›› 2025, Vol. 41 ›› Issue (3): 190-201.doi: 10.13560/j.cnki.biotech.bull.1985.2024-0820

Previous Articles    

Identification of the TCP Gene Family in Actinidia chinensis var. Hongyang and Their Expression Analysis in Fruit

SONG Shu-yi1,2(), JIANG Kai-xiu2, LIU Huan-yan2, HUANG Ya-cheng2(), LIU Lin-ya2()   

  1. 1.Life and Health College, Dalian University, Dalian 116622
    2.School of Biological Science and Technology, Liupanshui Normal University, Liupanshui 553004
  • Received:2024-08-23 Online:2025-03-26 Published:2025-03-20
  • Contact: HUANG Ya-cheng, LIU Lin-ya E-mail:ishuyisong@163.com;yachenghuang1314@126.com;liulinya913@126.com

Abstract:

Objective The members of TEOSINTE-BRANCHED1/CYCLOIDEA/PCF in kiwifruit ‘Hongyang’ (Actinidia chinensis var. Hongyang) (AcTCPs) gene family were identified based on whole-genome. Taxonomic and evolutionary relationships of the members were analyzed, and the expression profiles of the AcTCP genes in tissue-specific expression, fruit development process, and hormones treatments were explored. These findings provide a basis for further exploring the function of the AcTCP gene in kiwifruit. Method Bioinformatics methods were used to analyze the physicochemical properties, gene structure, conserved motifs, cis-acting elements and inter-species covariance of TCP transcription factors in kiwifruit ‘Hongyang’ were analyzed. RNA-seq and RT-qPCR were used to investigate the expression profiles of AcTCPs in different tissues, fruit development and in response to hormonal stimuli. Result A total of 40 AcTCP genes with complete TCP domains were identified on19 chromosomes in kiwifruit ‘Hongyang’ and named AcTCP1-AcTCP40. Using phylogenetic analyses, conserved motif, and gene structure analyses, the family members were divided into PCF (21), CIN (12) and CYC/TB1 (7). Synteny analysis showed that genome-wide or segment-based replication played an important role in the expansion of the kiwifruit ‘Hongyang’ TCP gene family. Analysis of tissue-specificity showed that the six candidate genes expressed significantly high in male flowers and fruits. The results of RT-qPCR experiments at different stages of fruit development found that AcTCP1 showed elevated expressions at later stages of fruit development, while AcTCP11, AcTCP35, AcTCP10, and AcTCP32 demonstrated high expression during the initial stages of fruit development, and the expression pattern was consistent with the transcriptomic results. In fruit, abscisic acid (ABA) and ethylene (ET) treatments to the fruits down-regulated six candidate AcTCPs, gibberellin (GA3) treatment up-regulated the expressions of AcTCP1, AcTCP35 and AcTCP32, and the forchlorfenuron (CPPU) treatment up-regulated the expressions of AcTCP1, AcTCP35 and AcTCP32 in initial stages, whereas GA3 and CPPU decreased the expressions of the others AcTCPs. Conclusion A total of 40 TCP members from kiwifruit ‘Hongyang’ were systematically identified. The expression patterns of six candidate genes highly express in the fruit and male flowers. The expressions of AcTCP35, AcTCP32, AcTCP1, AcTCP10, AcTCP11 and AcTCP20 in the fruit are involved in kiwifruit development and are regulated by various exogenous hormones (ABA, ET, GA3, and CPPU).

Key words: Actinidia chinensis var. Hongyang, TCP transcription factors, genome-wide identification, bioinformatics, organizational differences, expression pattern analysis, hormone treatment