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Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera

Calotropis procera is a medicinal plant of immense importance due to its pharmaceutical active components, especially cardiac glycosides (CG). As genomic resources for this plant are limited, the genes involved in CG biosynthetic pathway remain largely unknown till date. Our study on stage and tissu...

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Autores principales: Pandey, Akansha, Swarnkar, Vishakha, Pandey, Tushar, Srivastava, Piush, Kanojiya, Sanjeev, Mishra, Dipak Kumar, Tripathi, Vineeta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050527/
https://www.ncbi.nlm.nih.gov/pubmed/27703261
http://dx.doi.org/10.1038/srep34464
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author Pandey, Akansha
Swarnkar, Vishakha
Pandey, Tushar
Srivastava, Piush
Kanojiya, Sanjeev
Mishra, Dipak Kumar
Tripathi, Vineeta
author_facet Pandey, Akansha
Swarnkar, Vishakha
Pandey, Tushar
Srivastava, Piush
Kanojiya, Sanjeev
Mishra, Dipak Kumar
Tripathi, Vineeta
author_sort Pandey, Akansha
collection PubMed
description Calotropis procera is a medicinal plant of immense importance due to its pharmaceutical active components, especially cardiac glycosides (CG). As genomic resources for this plant are limited, the genes involved in CG biosynthetic pathway remain largely unknown till date. Our study on stage and tissue specific metabolite accumulation showed that CG’s were maximally accumulated in stems of 3 month old seedlings. De novo transcriptome sequencing of same was done using high throughput Illumina HiSeq platform generating 44074 unigenes with average mean length of 1785 base pair. Around 66.6% of unigenes were annotated by using various public databases and 5324 unigenes showed significant match in the KEGG database involved in 133 different pathways of plant metabolism. Further KEGG analysis resulted in identification of 336 unigenes involved in cardenolide biosynthesis. Tissue specific expression analysis of 30 putative transcripts involved in terpenoid, steroid and cardenolide pathways showed a positive correlation between metabolite and transcript accumulation. Wound stress elevated CG levels as well the levels of the putative transcripts involved in its biosynthetic pathways. This result further validated the involvement of identified transcripts in CGs biosynthesis. The identified transcripts will lay a substantial foundation for further research on metabolic engineering and regulation of cardiac glycosides biosynthesis pathway genes.
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spelling pubmed-50505272016-10-11 Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera Pandey, Akansha Swarnkar, Vishakha Pandey, Tushar Srivastava, Piush Kanojiya, Sanjeev Mishra, Dipak Kumar Tripathi, Vineeta Sci Rep Article Calotropis procera is a medicinal plant of immense importance due to its pharmaceutical active components, especially cardiac glycosides (CG). As genomic resources for this plant are limited, the genes involved in CG biosynthetic pathway remain largely unknown till date. Our study on stage and tissue specific metabolite accumulation showed that CG’s were maximally accumulated in stems of 3 month old seedlings. De novo transcriptome sequencing of same was done using high throughput Illumina HiSeq platform generating 44074 unigenes with average mean length of 1785 base pair. Around 66.6% of unigenes were annotated by using various public databases and 5324 unigenes showed significant match in the KEGG database involved in 133 different pathways of plant metabolism. Further KEGG analysis resulted in identification of 336 unigenes involved in cardenolide biosynthesis. Tissue specific expression analysis of 30 putative transcripts involved in terpenoid, steroid and cardenolide pathways showed a positive correlation between metabolite and transcript accumulation. Wound stress elevated CG levels as well the levels of the putative transcripts involved in its biosynthetic pathways. This result further validated the involvement of identified transcripts in CGs biosynthesis. The identified transcripts will lay a substantial foundation for further research on metabolic engineering and regulation of cardiac glycosides biosynthesis pathway genes. Nature Publishing Group 2016-10-05 /pmc/articles/PMC5050527/ /pubmed/27703261 http://dx.doi.org/10.1038/srep34464 Text en Copyright © 2016, The Author(s) 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
Pandey, Akansha
Swarnkar, Vishakha
Pandey, Tushar
Srivastava, Piush
Kanojiya, Sanjeev
Mishra, Dipak Kumar
Tripathi, Vineeta
Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera
title Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera
title_full Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera
title_fullStr Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera
title_full_unstemmed Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera
title_short Transcriptome and Metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from Calotropis procera
title_sort transcriptome and metabolite analysis reveal candidate genes of the cardiac glycoside biosynthetic pathway from calotropis procera
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050527/
https://www.ncbi.nlm.nih.gov/pubmed/27703261
http://dx.doi.org/10.1038/srep34464
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