Abstract

The blood red color of pigmented orange fruit varieties [Citrus sinensis L. (Osbeck)] is due to the presence of anthocyanin pigments that largely contribute to determine the high organoleptic qualities and the nutritional properties of the fruits. The content of pigments in sweet orange depends primarily on genetic factors and on environmental conditions. In particular, it has been extensively shown that cold temperature induces an increase of anthocyanin content that is achieved by the induction of the related gene expression. The purpose of our work is to understand the mechanism underlying the color variegation occurring inside the blood oranges during the cold induction of anthocyanin biosynthesis, despite the fact that the entire fruit is genotypically programmed to produce pigments. Therefore, the amount of anthocyanin and the expression of both structural and regulatory genes have been monitored in either high-pigmented (HP) or not/low pigmented (NP) segments of the same fruit during the storage at 4 °C for a total experimental period of 25 days. Our results clearly indicate that the anthocyanin content is directly correlated with the levels of gene transcription, with higher pigmented areas showing higher enhancement of gene expression. Furthermore, we analyzed the reshaping of the DNA methylation status at the promoter regions of genes related to anthocyanin biosynthetic pathway, such as DFR and Ruby. Our results unequivocally demonstrate that in the promoter regions of both DFR and Ruby, the amount of cytosine methylation strongly decreases along the cold storage in the HP areas, whereas it increases in the NP areas of the same fruit, probably causing a partial block of the gene transcription. Finally, by measuring the changes in the expression levels of the Citrus DNA demethylases, we found that DML1 might play a crucial role in determining the observed demethylation of DFR and Ruby promoters, with its expression induced by cold in the HP areas of the fruits. This is the first report in which different levels of gene expression implicated in anthocyanin production in blood orange fruit is correlated with an epigenetic control mechanism such as promoter methylation.

Highlights

  • Anthocyanins are water-soluble pigments belonging to the flavonoid compound family concerned in numerous aspects of plant development and defense

  • The analysis of the pigmentation of the blood orange varieties has been subject of many researches and has clarified the pathway leading to anthocyanin biosynthesis and its regulation.[1]

  • The effect of low temperature upon the anthocyanin biosynthesis has been studied in depth, ascertaining that pigment levels increase in response to cold storage due to the induction of structural genes involved in their biosynthesis,[1,4−6] as well as to the enhancement of Ruby expression.[11]

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Summary

Introduction

Anthocyanins are water-soluble pigments belonging to the flavonoid compound family concerned in numerous aspects of plant development and defense. Osbeck], which include Tarocco, Moro, and Sanguinello are able to synthesize anthocyanins which confer to the fruit the characteristic bloody color and make them distinguishable from the nonpigmented, blond orange varieties.[1] Anthocyanins are synthesized via the flavonoid pathway, which is a ubiquitous and well-described plant secondary metabolism pathway.[2] Most genes encoding the enzymes that biosynthesize the pigment molecules have been cloned and characterized in various species,[3] the Citrus species included.[1,4−7] Phenylalanine is a direct precursor for the synthesis of anthocyanidins and its conversion to the pigment core structure requires a series of reactions. Anthocyanidin synthase (ANS) converts the colorless leucoanthocyanidins into the colored anthocyanidins, that, once formed, are immediately modified by the UDP-glucoseflavonoid glucosyl transferase (UFGT) that catalyzes the addition of a glucose molecule in the 3-OH positions of Received: April 14, 2020 Revised: June 10, 2020 Accepted: June 10, 2020 Published: June 10, 2020

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