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RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua

Cinnamate-4-hydroxylase (C4H) converts trans-cinnamic acid (CA) to p-coumaric acid (COA) in the phenylpropanoid/lignin biosynthesis pathway. Earlier we reported increased expression of AaCYP71AV1 (an important gene of artemisinin biosynthesis pathway) caused by CA treatment in Artemisia annua. Hence...

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Autores principales: Kumar, Ritesh, Vashisth, Divya, Misra, Amita, Akhtar, Md Qussen, Jalil, Syed Uzma, Shanker, Karuna, Gupta, Madan Mohan, Rout, Prashant Kumar, Gupta, Anil Kumar, Shasany, Ajit Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879530/
https://www.ncbi.nlm.nih.gov/pubmed/27220407
http://dx.doi.org/10.1038/srep26458
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author Kumar, Ritesh
Vashisth, Divya
Misra, Amita
Akhtar, Md Qussen
Jalil, Syed Uzma
Shanker, Karuna
Gupta, Madan Mohan
Rout, Prashant Kumar
Gupta, Anil Kumar
Shasany, Ajit Kumar
author_facet Kumar, Ritesh
Vashisth, Divya
Misra, Amita
Akhtar, Md Qussen
Jalil, Syed Uzma
Shanker, Karuna
Gupta, Madan Mohan
Rout, Prashant Kumar
Gupta, Anil Kumar
Shasany, Ajit Kumar
author_sort Kumar, Ritesh
collection PubMed
description Cinnamate-4-hydroxylase (C4H) converts trans-cinnamic acid (CA) to p-coumaric acid (COA) in the phenylpropanoid/lignin biosynthesis pathway. Earlier we reported increased expression of AaCYP71AV1 (an important gene of artemisinin biosynthesis pathway) caused by CA treatment in Artemisia annua. Hence, AaC4H gene was identified, cloned, characterized and silenced in A. annua with the assumption that the elevated internal CA due to knock down may increase the artemisinin yield. Accumulation of trans-cinnamic acid in the plant due to AaC4H knockdown was accompanied with the reduction of p-coumaric acid, total phenolics, anthocyanin, cinnamate-4-hydroxylase (C4H) and phenylalanine ammonia lyase (PAL) activities but increase in salicylic acid (SA) and artemisinin. Interestingly, feeding trans-cinnamic acid to the RNAi line increased the level of artemisinin along with benzoic (BA) and SA with no effect on the downstream metabolites p-coumaric acid, coniferylaldehyde and sinapaldehyde, whereas p-coumaric acid feeding increased the content of downstream coniferylaldehyde and sinapaldehyde with no effect on BA, SA, trans-cinnamic acid or artemisinin. SA is reported earlier to be inducing the artemisinin yield. This report demonstrates the link between the phenylpropanoid/lignin pathway with artemisinin pathway through SA, triggered by accumulation of trans-cinnamic acid because of the blockage at C4H.
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spelling pubmed-48795302016-06-08 RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua Kumar, Ritesh Vashisth, Divya Misra, Amita Akhtar, Md Qussen Jalil, Syed Uzma Shanker, Karuna Gupta, Madan Mohan Rout, Prashant Kumar Gupta, Anil Kumar Shasany, Ajit Kumar Sci Rep Article Cinnamate-4-hydroxylase (C4H) converts trans-cinnamic acid (CA) to p-coumaric acid (COA) in the phenylpropanoid/lignin biosynthesis pathway. Earlier we reported increased expression of AaCYP71AV1 (an important gene of artemisinin biosynthesis pathway) caused by CA treatment in Artemisia annua. Hence, AaC4H gene was identified, cloned, characterized and silenced in A. annua with the assumption that the elevated internal CA due to knock down may increase the artemisinin yield. Accumulation of trans-cinnamic acid in the plant due to AaC4H knockdown was accompanied with the reduction of p-coumaric acid, total phenolics, anthocyanin, cinnamate-4-hydroxylase (C4H) and phenylalanine ammonia lyase (PAL) activities but increase in salicylic acid (SA) and artemisinin. Interestingly, feeding trans-cinnamic acid to the RNAi line increased the level of artemisinin along with benzoic (BA) and SA with no effect on the downstream metabolites p-coumaric acid, coniferylaldehyde and sinapaldehyde, whereas p-coumaric acid feeding increased the content of downstream coniferylaldehyde and sinapaldehyde with no effect on BA, SA, trans-cinnamic acid or artemisinin. SA is reported earlier to be inducing the artemisinin yield. This report demonstrates the link between the phenylpropanoid/lignin pathway with artemisinin pathway through SA, triggered by accumulation of trans-cinnamic acid because of the blockage at C4H. Nature Publishing Group 2016-05-25 /pmc/articles/PMC4879530/ /pubmed/27220407 http://dx.doi.org/10.1038/srep26458 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kumar, Ritesh
Vashisth, Divya
Misra, Amita
Akhtar, Md Qussen
Jalil, Syed Uzma
Shanker, Karuna
Gupta, Madan Mohan
Rout, Prashant Kumar
Gupta, Anil Kumar
Shasany, Ajit Kumar
RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua
title RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua
title_full RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua
title_fullStr RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua
title_full_unstemmed RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua
title_short RNAi down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in Artemisia annua
title_sort rnai down-regulation of cinnamate-4-hydroxylase increases artemisinin biosynthesis in artemisia annua
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879530/
https://www.ncbi.nlm.nih.gov/pubmed/27220407
http://dx.doi.org/10.1038/srep26458
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