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      Functional MYB transcription factor encoding gene AN2 is associated with anthocyanin biosynthesis in Lycium ruthenicum Murray

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          Abstract

          Background

          Lycium ruthenicum Murray is an important economic plant in China and contains higher levels of anthocyanins in its fruits than other Lyciums. However, the genetic mechanism of anthocyanin production in this plant is unknown.

          Results

          Based on previous transcriptome analysis, LrAN2 and LbAN2, encoding MYB transcription factors, were isolated from L. ruthenicum and L. barbarum, respectively. Both genes contained two introns, encoded 257 amino acids with two-Aa difference, and carried the unabridged HTH-MYB, MYB-like DNA-binding, and SANT domains. In the phylogenetic trees, LrAN2 and LbAN2 were found to be closely related to NtAN2, which regulates anthocyanin biosynthesis in tobacco. Overexpression of LrAN2 and LbAN2 induced anthocyanin biosynthesis in all tissues of tobacco. The anthocyanin content in the leaves of transgenic lines with LbAN2 was lower than LrAN2. It indicated that the function of LbAN2 was weaker than LrAN2. The AN2 transcript could be detected only in the fruits of L. ruthenicum and increased during fruit development, accompanied by anthocyanin accumulation. In natural population, the alleles LrAN2 and LrAN2 were associated strictly with L. ruthenicum and L. barbarum, respectively . Moreover, an AN2 genetic diversity study suggested that Lyciums with yellow, white, purple, and jujube red fruits were derived from L. ruthenicum.

          Conclusions

          Two AN2 alleles, from L. ruthenicum and L. barbarum, were functional MYB transcriptor regulating anthocyanin biosynthesis . The functional diversity and high expression level of LrAN2 could be the reason for high anthocyanin content in the fruit of L. ruthenicum. Lyciums with yellow, white, purple, and jujube red fruits were derived from L. ruthenicum based on AN2 sequence diversity. The results may be advantageous in identifying new varieties and breeding new cultivars.

          Electronic supplementary material

          The online version of this article (10.1186/s12870-019-1752-8) contains supplementary material, which is available to authorized users.

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          Most cited references32

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          The flavonoid biosynthetic pathway in Arabidopsis: structural and genetic diversity.

          Flavonoids are representative plant secondary products. In the model plant Arabidopsis thaliana, at least 54 flavonoid molecules (35 flavonols, 11 anthocyanins and 8 proanthocyanidins) are found. Scaffold structures of flavonoids in Arabidopsis are relatively simple. These include kaempferol, quercetin and isorhamnetin for flavonols, cyanidin for anthocyanins and epicatechin for proanthocyanidins. The chemical diversity of flavonoids increases enormously by tailoring reactions which modify these scaffolds, including glycosylation, methylation and acylation. Genes responsible for the formation of flavonoid aglycone structures and their subsequent modification reactions have been extensively characterized by functional genomic efforts - mostly the integration of transcriptomics and metabolic profiling followed by reverse genetic experimentation. This review describes the state-of-art of flavonoid biosynthetic pathway in Arabidopsis regarding both structural and genetic diversity, focusing on the genes encoding enzymes for the biosynthetic reactions and vacuole translocation. Copyright © 2013 Elsevier Masson SAS. All rights reserved.
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            The origin and behavior of mutable loci in maize.

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              Anthocyanins and their role in cancer prevention.

              Anthocyanins are the most abundant flavonoid constituents of fruits and vegetables. The conjugated bonds in their structures, which absorb light at about 500 nm, are the basis for the bright red, blue and purple colors of fruits and vegetables, as well as the autumn foliage of deciduous trees. The daily intake of anthocyanins in residents of the United States is estimated to be about 200 mg or about 9-fold higher than that of other dietary flavonoids. In this review, we summarize the latest developments on the anti-carcinogenic activities of anthocyanins and anthocyanin-rich extracts in cell culture models and in animal model tumor systems, and discuss their molecular mechanisms of action. We also suggest reasons for the apparent lack of correlation between the effectiveness of anthocyanins in laboratory model systems and in humans as evidenced by epidemiological studies. Future studies aimed at enhancing the absorption of anthocyanins and/or their metabolites are likely to be necessary for their ultimate use for chemoprevention of human cancer.
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                Author and article information

                Contributors
                laughing1898@icloud.com
                1390822410@qq.com
                lzg@nwipb.cas.cn
                2365669518@qq.com
                1448043722@qq.com
                289440499@qq.com
                qhsdweile@aliyun.com
                beyond_3862740@163.com
                blliu@nwipb.cas.cn
                Journal
                BMC Plant Biol
                BMC Plant Biol
                BMC Plant Biology
                BioMed Central (London )
                1471-2229
                29 April 2019
                29 April 2019
                2019
                : 19
                : 169
                Affiliations
                [1 ]Qinghai Province Key Laboratory of Crop Molecular Breeding, Xining, 810008 China
                [2 ]GRID grid.262246.6, State Key Laboratory of Plateau Ecology and Agriculture, , Qinghai University, ; Qinghai, Xining, 800010 China
                [3 ]ISNI 0000000119573309, GRID grid.9227.e, Key Laboratory of Adaptation and Evolution of Plateau Biota (AEPB), , Northwest Institute of Plateau Biology, Chinese Academy of Sciences, ; Qinghai, Xining, 810008 China
                [4 ]GRID grid.462704.3, College of Biologic and Geographic Sciences, , Qinghai Normal University, ; Qinghai, Xining, 810008 China
                Article
                1752
                10.1186/s12870-019-1752-8
                6489258
                31035916
                7693fd22-06ac-4e2f-9787-c504a3bea141
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 1 December 2018
                : 31 March 2019
                Funding
                Funded by: Qinghai Science and Technology Department
                Award ID: 2018-NK-133, 2018-ZJ-T08, 2018-ZJ-762, 2019-ZJ-982Q
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 31600262
                Award Recipient :
                Funded by: West Light Talent Program of the Chinese Academy of Sciences and the Open Project of the State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University
                Award ID: 2018-KF-06
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Plant science & Botany
                l. ruthenicum,l. barbarum,fruit color,anthocyanin biosynthesis,an2
                Plant science & Botany
                l. ruthenicum, l. barbarum, fruit color, anthocyanin biosynthesis, an2

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