Identification and expression profiling analysis of ascorbate peroxidase gene family in Actinidia chinensis (Hongyang)

• Published in: Journal of plant research 2020-09, Vol.133 (5), p.715-726
• Main Authors: Liao, Guang-Lian, Liu, Qing, Li, Yi-Qi, Zhong, Min, Huang, Chun-Hui, Jia, Dong-Feng, Xu, Xiao-Biao
• Format: Article
• Language: English
• Subjects: Actinidia; Actinidia chinensis; Amino acids; Antioxidants; Apx protein; Ascorbic acid; Bagging; Biomedical and Life Sciences; Chloroplasts; Chromosomes; Coils; Cultivars; Cytoplasm; Enzymes; Gene expression; Genomes; Hydrogen peroxide; Introns; Kiwifruit; L-Ascorbate peroxidase; Life Sciences; Lipids; Membrane proteins; Metabolism; Oxygen metabolism; Peroxidase; Phylogeny; Plant Biochemistry; Plant Ecology; Plant Physiology; Plant Sciences; Proteins; Regular Paper – Physiology/Biochemistry/Molecular and Cellular Biology; Structural analysis
• ISSN: 0918-9440; 1618-0860
• DOI: 10.1007/s10265-020-01206-y

Ascorbate peroxidase (APX) is one of the important antioxidant enzymes in the active oxygen metabolism pathway of plants and animals, especially it is the key enzyme to clear H 2 O 2 in chloroplast and the main enzyme of vitamin C metabolism. However, knowledge about APX gene family members and their evolutionary and functional characteristics in kiwifruit is limited. In this study, we identified 13 members of the APX gene family in the kiwifruit (cultivar: Hongyang) genome according the APX proteins conserved domain of Arabidopsis thaliana . Phylogenetic analysis by maximum likelihood split these 13 genes into four groups. The APX gene family members were distributed on nine chromosomes (Nos. 4, 5, 11, 13, 20, 21, 23, 25, 28). Most of the encoded hydrophilic and lipid-soluble enzymes were predicted to be located in the cytoplasm, nucleus and chloroplast. Among them, AcAPX4, AcAPX5, AcAPX8, AcAPX12 were transmembrane proteins, and AcAPX8 and AcAPX12 had the same transmembrane domain. The gene structure analysis showed that AcAPXs were composed of 4-22 introns, except that AcAPX10 was intron-free. Multiple expectation maximization for motif elicitation program (MEME) analyzed 13 APX protein sequences of Actinidia chinensis and identified 10 conserved motifs ranging in length from 15 to 50 amino acid residues. Additionally, the predicted secondary structures of the main motifs consisted of α-helix and random coils. The gene expression of fruits in different growth stages and bagging treatment were determined by qRT-PCR. The results showed that 8 AcAPXs had the highest expression levels during the color turning period and only the gene expression of AcAPX3 was consistent with the ascorbic acid content; five AcAPXs were consistent with the ascorbic acid content after bagging. Our data provided evolutionary and functional information of AcAPX gene family members and revealed the gene expression of different members in different growth stages and bagging treatments These results may be useful for future studies of the structures and functions of AcAPX family members.