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De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid

The anti-cancer vinblastine and vincristine alkaloids can only be naturally found in periwinkle (Catharanthus roseus). Both of these alkaloids' accumulations are known to be influenced by salicylic acid (SA). The transcriptome data to reveal the induction effect (s) of SA, however, seem restric...

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Autores principales: Soltani, Narges, Firouzabadi, Farhad Nazarian, Shafeinia, Alireza, Shirali, Masoud, Sadr, Ayeh Sadat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592577/
https://www.ncbi.nlm.nih.gov/pubmed/36280677
http://dx.doi.org/10.1038/s41598-022-20314-4
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author Soltani, Narges
Firouzabadi, Farhad Nazarian
Shafeinia, Alireza
Shirali, Masoud
Sadr, Ayeh Sadat
author_facet Soltani, Narges
Firouzabadi, Farhad Nazarian
Shafeinia, Alireza
Shirali, Masoud
Sadr, Ayeh Sadat
author_sort Soltani, Narges
collection PubMed
description The anti-cancer vinblastine and vincristine alkaloids can only be naturally found in periwinkle (Catharanthus roseus). Both of these alkaloids' accumulations are known to be influenced by salicylic acid (SA). The transcriptome data to reveal the induction effect (s) of SA, however, seem restricted at this time. In this study, the de novo approach of transcriptome assembly was performed on the RNA-Sequencing (RNA-Seq) data in C. roseus. The outcome demonstrated that SA treatment boosted the expression of all the genes in the Terpenoid Indole Alkaloids (TIAs) pathway that produces the vinblastine and vincristine alkaloids. These outcomes supported the time-course measurements of vincristine alkaloid, the end product of the TIAs pathway, and demonstrated that SA spray had a positive impact on transcription and alkaloid synthesis. Additionally, the abundance of transcription factor families including bHLH, C3H, C2H2, MYB, MYB-related, AP2/ ERF, NAC, bZIP, and WRKY suggests a role for a variety of transcription families in response to the SA stimuli. Di-nucleotide and tri-nucleotide SSRs were the most prevalent SSR markers in microsatellite analyses, making up 39% and 34% of all SSR markers, respectively, out of the 77,192 total SSRs discovered.
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spelling pubmed-95925772022-10-26 De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid Soltani, Narges Firouzabadi, Farhad Nazarian Shafeinia, Alireza Shirali, Masoud Sadr, Ayeh Sadat Sci Rep Article The anti-cancer vinblastine and vincristine alkaloids can only be naturally found in periwinkle (Catharanthus roseus). Both of these alkaloids' accumulations are known to be influenced by salicylic acid (SA). The transcriptome data to reveal the induction effect (s) of SA, however, seem restricted at this time. In this study, the de novo approach of transcriptome assembly was performed on the RNA-Sequencing (RNA-Seq) data in C. roseus. The outcome demonstrated that SA treatment boosted the expression of all the genes in the Terpenoid Indole Alkaloids (TIAs) pathway that produces the vinblastine and vincristine alkaloids. These outcomes supported the time-course measurements of vincristine alkaloid, the end product of the TIAs pathway, and demonstrated that SA spray had a positive impact on transcription and alkaloid synthesis. Additionally, the abundance of transcription factor families including bHLH, C3H, C2H2, MYB, MYB-related, AP2/ ERF, NAC, bZIP, and WRKY suggests a role for a variety of transcription families in response to the SA stimuli. Di-nucleotide and tri-nucleotide SSRs were the most prevalent SSR markers in microsatellite analyses, making up 39% and 34% of all SSR markers, respectively, out of the 77,192 total SSRs discovered. Nature Publishing Group UK 2022-10-24 /pmc/articles/PMC9592577/ /pubmed/36280677 http://dx.doi.org/10.1038/s41598-022-20314-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Soltani, Narges
Firouzabadi, Farhad Nazarian
Shafeinia, Alireza
Shirali, Masoud
Sadr, Ayeh Sadat
De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
title De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
title_full De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
title_fullStr De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
title_full_unstemmed De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
title_short De Novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
title_sort de novo transcriptome assembly and differential expression analysis of catharanthus roseus in response to salicylic acid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592577/
https://www.ncbi.nlm.nih.gov/pubmed/36280677
http://dx.doi.org/10.1038/s41598-022-20314-4
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