Transcriptome profiling helps to elucidate the mechanisms of ripening and epidermal senescence in passion fruit (Passiflora edulia Sims)

• Published in: PloS one Vol. 15; no. 9; p. e0236535
• Main Authors: Li, Changbao, Xin, Ming, Li, Li, He, Xuemei, Liu, Guoming, Li, Jiemin, Sheng, Jinfeng, Sun, Jian, Ansari, Mohammad
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 25.09.2020; Public Library of Science (PLoS)
• Subjects: Annotations; Antioxidants; Biology and Life Sciences; Biosynthesis; Catalase; Cell walls; Cellulase; Cellulose; Degradation; Enzymatic activity; Enzymes; Flavonoids; Fruits; Galactosidase; Gene expression; Gene sequencing; Genetic aspects; Humidity; Laboratories; Lignin; Metabolism; Observations; Passiflora; Passion fruit; Peroxidase; Physical Sciences; Physiology; Phytochemicals; Polygalacturonase; Preservatives; Respiration; Ribonucleic acid; Ripening; Ripening (Botany); RNA; Senescence; Signal transduction; Signaling; Species classification; Starch; Sucrose; Sugar; Superoxide dismutase; Transcription; Transcription (Genetics); Vegetables; β-Galactosidase; China
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0236535

Passion fruit (Passiflora edulia Sims), an important tropical and subtropical species, is classified as a respiration climacteric fruit, and its quality deteriorates rapidly after harvest. To elucidate the mechanisms involved in ripening and rapid fruit senescence, phytochemical characteristic analysis and RNA sequencing were performed in purple passion fruit with different treatments, that is, 1-methylcyclopropene (1-MCP) and preservative film (PF). Comprehensive functional annotation and KEGG enrichment analysis showed that starch and sucrose metabolism, plant hormone signal transduction, phenylpropanoid biosynthesis, flavonoid biosynthesis, and carotenoid biosynthesis were involved in fruit ripening. Treatment with PF and 1-MCP significantly affected the transcription levels of passion fruit during postharvest storage. A large number of differentially expressed unigenes (DEGs) were identified as significantly enriched in starch and sucrose metabolism, plant hormone signal transduction and phenylpropanoid biosynthesis at the postharvest stage. The PF and 1-MCP treatments increased superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD) gene expression levels and enzyme activities, accelerated lignin accumulation, and decreased [beta]-galactosidase ([beta]-Gal), polygalacturonase (PG) and cellulose activities and gene expression levels to delay cell wall degradation during fruit senescence. The RNA sequencing data for cell wall metabolism and hormone signal transduction pathway-related unigenes were verified by RT-qPCR. The results of this study indicate that the cell wall metabolism and hormone signaling pathways are closely related to passion fruit ripening. PF and 1-MCP treatment might inhibit ethylene signaling and regulate cell wall metabolism pathways to inhibit cell wall degradation. Our results demonstrate the involvement of ripening- and senescence-related networks in passion fruit ripening and may establish a foundation for future research investigating the effects of PF and 1-MCP treatment on fruit ripening.