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Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression

BACKGROUND: Water-soluble anthocyanin pigments are important ingredients in health-improving supplements and valuable for the food industry. Although great attention has been paid to the breeding and production of crops containing high levels of anthocyanin, genetic variation in red or purple cabbag...

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Autores principales: Song, Hayoung, Yi, Hankuil, Lee, Myungjin, Han, Ching-Tack, Lee, Jeongyeo, Kim, HyeRan, Park, Jong-In, Nou, Ill-Sup, Kim, Sun-Ju, Hur, Yoonkang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941660/
https://www.ncbi.nlm.nih.gov/pubmed/29739331
http://dx.doi.org/10.1186/s12870-018-1290-9
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author Song, Hayoung
Yi, Hankuil
Lee, Myungjin
Han, Ching-Tack
Lee, Jeongyeo
Kim, HyeRan
Park, Jong-In
Nou, Ill-Sup
Kim, Sun-Ju
Hur, Yoonkang
author_facet Song, Hayoung
Yi, Hankuil
Lee, Myungjin
Han, Ching-Tack
Lee, Jeongyeo
Kim, HyeRan
Park, Jong-In
Nou, Ill-Sup
Kim, Sun-Ju
Hur, Yoonkang
author_sort Song, Hayoung
collection PubMed
description BACKGROUND: Water-soluble anthocyanin pigments are important ingredients in health-improving supplements and valuable for the food industry. Although great attention has been paid to the breeding and production of crops containing high levels of anthocyanin, genetic variation in red or purple cabbages (Brassica oleracea var. capitata F. rubra) has not yet been characterized at the molecular level. In this study, we identified the mechanism responsible for the establishment of purple color in cabbages. RESULTS: BoMYBL2–1 is one of the regulatory genes in the anthocyanin biosynthesis pathway in cabbages. It is a repressor whose expression is inversely correlated to anthocyanin synthesis and is not detectable in purple cabbages. Sequence analysis of purple cabbages revealed that most lacked BoMYBL2–1 coding sequences, although a few had a substitution in the region of the promoter 347 bp upstream of the gene that was associated with an absence of BoMYBL2–1 expression. Lack of transcriptional activity of the substitution-containing promoter was confirmed using transgenic Arabidopsis plants transformed with promoter::GUS fusion constructs. The finding that the defect in BoMYBL2–1 expression was solely responsible for purple coloration in cabbages was further demonstrated using genomic PCR and RT-PCR analyses of many other structural and regulatory genes in anthocyanin biosynthesis. Molecular markers for purple cabbages were developed and validated using 69 cabbage lines. CONCLUSION: Expression of BoMYBL2–1 was inversely correlated to anthocyanin content, and purple color in cabbages resulted from a loss of BoMYBL2–1 expression, caused by either the promoter substitution or deletion of the gene. This is the first report of molecular markers that distinguish purple cabbages. Such markers will be useful for the production of intraspecific and interspecific hybrids for functional foods, and for industrial purposes requiring high anthocyanin content. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1290-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-59416602018-05-14 Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression Song, Hayoung Yi, Hankuil Lee, Myungjin Han, Ching-Tack Lee, Jeongyeo Kim, HyeRan Park, Jong-In Nou, Ill-Sup Kim, Sun-Ju Hur, Yoonkang BMC Plant Biol Research Article BACKGROUND: Water-soluble anthocyanin pigments are important ingredients in health-improving supplements and valuable for the food industry. Although great attention has been paid to the breeding and production of crops containing high levels of anthocyanin, genetic variation in red or purple cabbages (Brassica oleracea var. capitata F. rubra) has not yet been characterized at the molecular level. In this study, we identified the mechanism responsible for the establishment of purple color in cabbages. RESULTS: BoMYBL2–1 is one of the regulatory genes in the anthocyanin biosynthesis pathway in cabbages. It is a repressor whose expression is inversely correlated to anthocyanin synthesis and is not detectable in purple cabbages. Sequence analysis of purple cabbages revealed that most lacked BoMYBL2–1 coding sequences, although a few had a substitution in the region of the promoter 347 bp upstream of the gene that was associated with an absence of BoMYBL2–1 expression. Lack of transcriptional activity of the substitution-containing promoter was confirmed using transgenic Arabidopsis plants transformed with promoter::GUS fusion constructs. The finding that the defect in BoMYBL2–1 expression was solely responsible for purple coloration in cabbages was further demonstrated using genomic PCR and RT-PCR analyses of many other structural and regulatory genes in anthocyanin biosynthesis. Molecular markers for purple cabbages were developed and validated using 69 cabbage lines. CONCLUSION: Expression of BoMYBL2–1 was inversely correlated to anthocyanin content, and purple color in cabbages resulted from a loss of BoMYBL2–1 expression, caused by either the promoter substitution or deletion of the gene. This is the first report of molecular markers that distinguish purple cabbages. Such markers will be useful for the production of intraspecific and interspecific hybrids for functional foods, and for industrial purposes requiring high anthocyanin content. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1290-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-08 /pmc/articles/PMC5941660/ /pubmed/29739331 http://dx.doi.org/10.1186/s12870-018-1290-9 Text en © The Author(s). 2018 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.
spellingShingle Research Article
Song, Hayoung
Yi, Hankuil
Lee, Myungjin
Han, Ching-Tack
Lee, Jeongyeo
Kim, HyeRan
Park, Jong-In
Nou, Ill-Sup
Kim, Sun-Ju
Hur, Yoonkang
Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression
title Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression
title_full Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression
title_fullStr Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression
title_full_unstemmed Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression
title_short Purple Brassica oleracea var. capitata F. rubra is due to the loss of BoMYBL2–1 expression
title_sort purple brassica oleracea var. capitata f. rubra is due to the loss of bomybl2–1 expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941660/
https://www.ncbi.nlm.nih.gov/pubmed/29739331
http://dx.doi.org/10.1186/s12870-018-1290-9
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