Cargando…
PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1
Saponins are the main triterpenoid ingredients from Panax notoginseng, a well-known Chinese medicine, and are important sources for producing drugs to prevent and treat cerebrovascular and cardiovascular diseases. However, the transcriptional regulatory network of saponin biosynthesis in P. notogins...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410195/ https://www.ncbi.nlm.nih.gov/pubmed/37564268 http://dx.doi.org/10.1093/hr/uhad134 |
_version_ | 1785086403177086976 |
---|---|
author | Man, Jinhui Shi, Yue Huang, Yuying Zhang, Xiaoqin Wang, Xin Liu, Shanhu He, Gaojie An, Kelu Han, Dongran Wang, Xiaohui Wei, Shengli |
author_facet | Man, Jinhui Shi, Yue Huang, Yuying Zhang, Xiaoqin Wang, Xin Liu, Shanhu He, Gaojie An, Kelu Han, Dongran Wang, Xiaohui Wei, Shengli |
author_sort | Man, Jinhui |
collection | PubMed |
description | Saponins are the main triterpenoid ingredients from Panax notoginseng, a well-known Chinese medicine, and are important sources for producing drugs to prevent and treat cerebrovascular and cardiovascular diseases. However, the transcriptional regulatory network of saponin biosynthesis in P. notoginseng is largely unknown. In the present study we demonstrated that one R2R3-MYB transcription factor, designated PnMYB4, acts as a repressor of saponin accumulation. Suppression of PnMYB4 in P. notoginseng calli significantly increased the saponin content and the expression level of saponin biosynthetic genes. PnMYB4 directly bound to the promoters of key saponin biosynthetic genes, including PnSS, PnSE, and PnDS, to repress saponin accumulation. PnMYB4 and the activator PnMYB1 could interacted with PnbHLH, which is a positive regulator of saponin biosynthesis, to modulate the biosynthesis of saponin. PnMYB4 competed with PnMYB1 for binding to PnbHLH, repressing activation of the promoters of saponin structural genes induced by the PnMYB1-PnbHLH complex. Our study reveals that a complex regulatory module of saponin biosynthesis is associated with positive and negative MYB transcriptional regulators and provides a theoretical basis for improving the content of saponins and efficacy of P. notoginseng. |
format | Online Article Text |
id | pubmed-10410195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104101952023-08-10 PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 Man, Jinhui Shi, Yue Huang, Yuying Zhang, Xiaoqin Wang, Xin Liu, Shanhu He, Gaojie An, Kelu Han, Dongran Wang, Xiaohui Wei, Shengli Hortic Res Article Saponins are the main triterpenoid ingredients from Panax notoginseng, a well-known Chinese medicine, and are important sources for producing drugs to prevent and treat cerebrovascular and cardiovascular diseases. However, the transcriptional regulatory network of saponin biosynthesis in P. notoginseng is largely unknown. In the present study we demonstrated that one R2R3-MYB transcription factor, designated PnMYB4, acts as a repressor of saponin accumulation. Suppression of PnMYB4 in P. notoginseng calli significantly increased the saponin content and the expression level of saponin biosynthetic genes. PnMYB4 directly bound to the promoters of key saponin biosynthetic genes, including PnSS, PnSE, and PnDS, to repress saponin accumulation. PnMYB4 and the activator PnMYB1 could interacted with PnbHLH, which is a positive regulator of saponin biosynthesis, to modulate the biosynthesis of saponin. PnMYB4 competed with PnMYB1 for binding to PnbHLH, repressing activation of the promoters of saponin structural genes induced by the PnMYB1-PnbHLH complex. Our study reveals that a complex regulatory module of saponin biosynthesis is associated with positive and negative MYB transcriptional regulators and provides a theoretical basis for improving the content of saponins and efficacy of P. notoginseng. Oxford University Press 2023-07-05 /pmc/articles/PMC10410195/ /pubmed/37564268 http://dx.doi.org/10.1093/hr/uhad134 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nanjing Agricultural University. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Man, Jinhui Shi, Yue Huang, Yuying Zhang, Xiaoqin Wang, Xin Liu, Shanhu He, Gaojie An, Kelu Han, Dongran Wang, Xiaohui Wei, Shengli PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 |
title | PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 |
title_full | PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 |
title_fullStr | PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 |
title_full_unstemmed | PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 |
title_short | PnMYB4 negatively modulates saponin biosynthesis in Panax notoginseng through interplay with PnMYB1 |
title_sort | pnmyb4 negatively modulates saponin biosynthesis in panax notoginseng through interplay with pnmyb1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410195/ https://www.ncbi.nlm.nih.gov/pubmed/37564268 http://dx.doi.org/10.1093/hr/uhad134 |
work_keys_str_mv | AT manjinhui pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT shiyue pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT huangyuying pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT zhangxiaoqin pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT wangxin pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT liushanhu pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT hegaojie pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT ankelu pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT handongran pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT wangxiaohui pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 AT weishengli pnmyb4negativelymodulatessaponinbiosynthesisinpanaxnotoginsengthroughinterplaywithpnmyb1 |