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RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.)
Anthocyanins are water-soluble plant pigments mainly stored in the plant vacuoles. Glutathione S-transferases (GSTs) are a multifunctional enzyme family, which can regulate substance metabolism and biological and abiotic stresses in plants. However, few reports were focused on the involvement of GST...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289562/ https://www.ncbi.nlm.nih.gov/pubmed/35860534 http://dx.doi.org/10.3389/fpls.2022.870202 |
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author | Niu, Mengyang Bao, Changjian Chen, Jiahui Zhou, Wen Zhang, Yueyue Zhang, Xiaoyan Su, Nana Cui, Jin |
author_facet | Niu, Mengyang Bao, Changjian Chen, Jiahui Zhou, Wen Zhang, Yueyue Zhang, Xiaoyan Su, Nana Cui, Jin |
author_sort | Niu, Mengyang |
collection | PubMed |
description | Anthocyanins are water-soluble plant pigments mainly stored in the plant vacuoles. Glutathione S-transferases (GSTs) are a multifunctional enzyme family, which can regulate substance metabolism and biological and abiotic stresses in plants. However, few reports were focused on the involvement of GSTs in anthocyanin sequestration in red skin radish. Here, we identified a glutathione S-transferase gene RsGSTF12 that played roles in anthocyanin sequestration in radish. The bioinformatics analysis revealed that RsGSTF12 belonged to the phi (F) class of glutathione S-transferases and showed a high homology with AtGSTF12, followed by AtGSTF11. The subcellular localization assay showed that RsGSTF12 was located in the endoplasmic reticulum and tonoplast. Temporal and spatial gene expression-specific analyses uncovered a strong correlation of RsGSTF12 with anthocyanin accumulation in radish sprouts. The anthocyanin solubility assay found RsGSTF12 was capable of improving cyanidin water solubility in vitro. Transiently expressing RsGSTF12 in radish cotyledons was able to increase their anthocyanin sequestrations. Furthermore, the functional complementation and overexpression of the Arabidopsis thaliana tt19 mutant and wild type demonstrated that RsGSTF12 might play an indispensable role in anthocyanin accumulation in radish. Taken together, we provide compelling evidence that RsGSTF12 functions critically in how anthocyanins are sequestrated in radish, which may enrich our understanding of the mechanism of anthocyanin sequestration. |
format | Online Article Text |
id | pubmed-9289562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92895622022-07-19 RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) Niu, Mengyang Bao, Changjian Chen, Jiahui Zhou, Wen Zhang, Yueyue Zhang, Xiaoyan Su, Nana Cui, Jin Front Plant Sci Plant Science Anthocyanins are water-soluble plant pigments mainly stored in the plant vacuoles. Glutathione S-transferases (GSTs) are a multifunctional enzyme family, which can regulate substance metabolism and biological and abiotic stresses in plants. However, few reports were focused on the involvement of GSTs in anthocyanin sequestration in red skin radish. Here, we identified a glutathione S-transferase gene RsGSTF12 that played roles in anthocyanin sequestration in radish. The bioinformatics analysis revealed that RsGSTF12 belonged to the phi (F) class of glutathione S-transferases and showed a high homology with AtGSTF12, followed by AtGSTF11. The subcellular localization assay showed that RsGSTF12 was located in the endoplasmic reticulum and tonoplast. Temporal and spatial gene expression-specific analyses uncovered a strong correlation of RsGSTF12 with anthocyanin accumulation in radish sprouts. The anthocyanin solubility assay found RsGSTF12 was capable of improving cyanidin water solubility in vitro. Transiently expressing RsGSTF12 in radish cotyledons was able to increase their anthocyanin sequestrations. Furthermore, the functional complementation and overexpression of the Arabidopsis thaliana tt19 mutant and wild type demonstrated that RsGSTF12 might play an indispensable role in anthocyanin accumulation in radish. Taken together, we provide compelling evidence that RsGSTF12 functions critically in how anthocyanins are sequestrated in radish, which may enrich our understanding of the mechanism of anthocyanin sequestration. Frontiers Media S.A. 2022-07-04 /pmc/articles/PMC9289562/ /pubmed/35860534 http://dx.doi.org/10.3389/fpls.2022.870202 Text en Copyright © 2022 Niu, Bao, Chen, Zhou, Zhang, Zhang, Su and Cui. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Niu, Mengyang Bao, Changjian Chen, Jiahui Zhou, Wen Zhang, Yueyue Zhang, Xiaoyan Su, Nana Cui, Jin RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) |
title | RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) |
title_full | RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) |
title_fullStr | RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) |
title_full_unstemmed | RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) |
title_short | RsGSTF12 Contributes to Anthocyanin Sequestration in Radish (Raphanus sativus L.) |
title_sort | rsgstf12 contributes to anthocyanin sequestration in radish (raphanus sativus l.) |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289562/ https://www.ncbi.nlm.nih.gov/pubmed/35860534 http://dx.doi.org/10.3389/fpls.2022.870202 |
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