Abstract

A remarkable characteristic of pineapple is its ability to undergo floral induction in response to external ethylene stimulation. However, little information is available regarding the molecular mechanism underlying this process. In this study, the differentially expressed genes (DEGs) in plants exposed to 1.80 mL·L−1 (T1) or 2.40 mL·L−1 ethephon (T2) compared with Ct plants (control, cleaning water) were identified using RNA-seq and gene expression profiling. Illumina sequencing generated 65,825,224 high-quality reads that were assembled into 129,594 unigenes with an average sequence length of 1173 bp. Of these unigenes, 24,775 were assigned to specific KEGG pathways, of which metabolic pathways and biosynthesis of secondary metabolites were the most highly represented. Gene Ontology (GO) analysis of the annotated unigenes revealed that the majority were involved in metabolic and cellular processes, cell and cell part, catalytic activity and binding. Gene expression profiling analysis revealed 3788, 3062, and 758 DEGs in the comparisons of T1 with Ct, T2 with Ct, and T2 with T1, respectively. GO analysis indicated that these DEGs were predominantly annotated to metabolic and cellular processes, cell and cell part, catalytic activity, and binding. KEGG pathway analysis revealed the enrichment of several important pathways among the DEGs, including metabolic pathways, biosynthesis of secondary metabolites and plant hormone signal transduction. Thirteen DEGs were identified as candidate genes associated with the process of floral induction by ethephon, including three ERF-like genes, one ETR-like gene, one LTI-like gene, one FT-like gene, one VRN1-like gene, three FRI-like genes, one AP1-like gene, one CAL-like gene, and one AG-like gene. qPCR analysis indicated that the changes in the expression of these 13 candidate genes were consistent with the alterations in the corresponding RPKM values, confirming the accuracy and credibility of the RNA-seq and gene expression profiling results. Ethephon-mediated induction likely mimics the process of vernalization in the floral transition in pineapple by increasing LTI, FT, and VRN1 expression and promoting the up-regulation of floral meristem identity genes involved in flower development. The candidate genes screened can be used in investigations of the molecular mechanisms of the flowering pathway and of various other biological mechanisms in pineapple.

Highlights

  • Pineapple [Ananas comosus (L.) Merr.], which is indigenous to Brazil, Argentina and Paraguay, has been introduced worldwide and is the leading edible member of the Bromeliaceae family (Smith and Downs, 1974)

  • The Gene Ontology (GO) annotations of the differentially expressed genes (DEGs) revealed that the metabolic process and cellular process categories of the biological process ontology were predominant, as well as cell, cell part and organelle in the cellular component ontology, and catalytic activity and binding in the molecular function ontology

  • KEGG pathway analysis indicated that metabolic pathways, biosynthesis of secondary metabolites, and plant hormone signal transduction were enriched among the DEGs

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Summary

Introduction

Pineapple [Ananas comosus (L.) Merr.], which is indigenous to Brazil, Argentina and Paraguay, has been introduced worldwide and is the leading edible member of the Bromeliaceae family (Smith and Downs, 1974) It is an economically important tropical herbaceous fruit with attractive sensorial and nutritional characteristics (Coppens d’Eeckenbrugge and Leal, 2003). In pineapple and other bromeliads, it has been proposed that flowering is triggered by a small burst of ethylene production in the meristem in response to environmental cues (Trusov and Botella, 2006) This feature is exploited worldwide by commercial pineapple growers to synchronize flower and fruit development, resulting in a single harvest pass. With the use of ethephon for flower induction, pineapple can be fruited and harvested multiple times per year (Liu and Liu, 2014)

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