Cargando…

LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway

Anthocyanin-derived fleshy fruit pigmentation has become an excellent system for studying the regulatory network underlying fruit ripening and quality. The transcriptional control of anthocyanin biosynthesis by MYB–bHLH–WDR complexes has been well established, but the intermediate signals through wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Gen, Qin, Beibei, Li, Shuodan, Yin, Yue, Zhao, Jianhua, An, Wei, Cao, Youlong, Mu, Zixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438876/
https://www.ncbi.nlm.nih.gov/pubmed/32903673
http://dx.doi.org/10.3389/fpls.2020.01215
_version_ 1783572880346316800
author Li, Gen
Qin, Beibei
Li, Shuodan
Yin, Yue
Zhao, Jianhua
An, Wei
Cao, Youlong
Mu, Zixin
author_facet Li, Gen
Qin, Beibei
Li, Shuodan
Yin, Yue
Zhao, Jianhua
An, Wei
Cao, Youlong
Mu, Zixin
author_sort Li, Gen
collection PubMed
description Anthocyanin-derived fleshy fruit pigmentation has become an excellent system for studying the regulatory network underlying fruit ripening and quality. The transcriptional control of anthocyanin biosynthesis by MYB–bHLH–WDR complexes has been well established, but the intermediate signals through which the environmental or developmental cues regulate these transcription factors remain poorly understood. Here we found that nitric oxide (NO) production during Lycium fruit ripening decreased progressively presenting a negative relationship with anthocyanins. After cloning of the nitric reductase (NR) gene from Lycium barbarum (LbNR) plants, we demonstrated that LbNR-derived NO partially inhibited anthocyanin biosynthesis but enhanced proanthocyanidin (PA) accumulation, and delayed fruit coloration. Application of the NO donor, sodium nitroprusside (SNP), produced a similar effect. The endogenous or exogenous NO downregulated the transcripts both of the regulatory genes and the structural genes that related to anthocyanin biosynthesis, while upregulated both of those genes that related to PA biosynthesis. Given there is a significant negative relationship between the levels of anthocyanins and PAs during Lycium fruit ripening, NO not only inhibited anthocyanin de novo biosynthesis but redirected the flavonoid biosynthetic pathway from anthocyanins to PA production. Two types of LrMYB transcription factors of opposite nature, namely anthocyanin-specific and PA-specific, which belong to the R2R3-MYB subfamily and 1R-MYB subfamily, respectively, were identified from L. ruthenicum fruits. It was further found that NO acts by antagonizing the ABA signaling, a phytohormone we have previously shown playing a positive role in Lycium fruit coloration. Our results provided particularly novel information about NO–ABA–anthocyanin interplay during Lycium fruit development and ripening, which may fill a gap between the developmental cues and the transcriptional regulation of anthocyanin biosynthesis.
format Online
Article
Text
id pubmed-7438876
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-74388762020-09-03 LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway Li, Gen Qin, Beibei Li, Shuodan Yin, Yue Zhao, Jianhua An, Wei Cao, Youlong Mu, Zixin Front Plant Sci Plant Science Anthocyanin-derived fleshy fruit pigmentation has become an excellent system for studying the regulatory network underlying fruit ripening and quality. The transcriptional control of anthocyanin biosynthesis by MYB–bHLH–WDR complexes has been well established, but the intermediate signals through which the environmental or developmental cues regulate these transcription factors remain poorly understood. Here we found that nitric oxide (NO) production during Lycium fruit ripening decreased progressively presenting a negative relationship with anthocyanins. After cloning of the nitric reductase (NR) gene from Lycium barbarum (LbNR) plants, we demonstrated that LbNR-derived NO partially inhibited anthocyanin biosynthesis but enhanced proanthocyanidin (PA) accumulation, and delayed fruit coloration. Application of the NO donor, sodium nitroprusside (SNP), produced a similar effect. The endogenous or exogenous NO downregulated the transcripts both of the regulatory genes and the structural genes that related to anthocyanin biosynthesis, while upregulated both of those genes that related to PA biosynthesis. Given there is a significant negative relationship between the levels of anthocyanins and PAs during Lycium fruit ripening, NO not only inhibited anthocyanin de novo biosynthesis but redirected the flavonoid biosynthetic pathway from anthocyanins to PA production. Two types of LrMYB transcription factors of opposite nature, namely anthocyanin-specific and PA-specific, which belong to the R2R3-MYB subfamily and 1R-MYB subfamily, respectively, were identified from L. ruthenicum fruits. It was further found that NO acts by antagonizing the ABA signaling, a phytohormone we have previously shown playing a positive role in Lycium fruit coloration. Our results provided particularly novel information about NO–ABA–anthocyanin interplay during Lycium fruit development and ripening, which may fill a gap between the developmental cues and the transcriptional regulation of anthocyanin biosynthesis. Frontiers Media S.A. 2020-08-13 /pmc/articles/PMC7438876/ /pubmed/32903673 http://dx.doi.org/10.3389/fpls.2020.01215 Text en Copyright © 2020 Li, Qin, Li, Yin, Zhao, An, Cao and Mu http://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
Li, Gen
Qin, Beibei
Li, Shuodan
Yin, Yue
Zhao, Jianhua
An, Wei
Cao, Youlong
Mu, Zixin
LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway
title LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway
title_full LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway
title_fullStr LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway
title_full_unstemmed LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway
title_short LbNR-Derived Nitric Oxide Delays Lycium Fruit Coloration by Transcriptionally Modifying Flavonoid Biosynthetic Pathway
title_sort lbnr-derived nitric oxide delays lycium fruit coloration by transcriptionally modifying flavonoid biosynthetic pathway
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438876/
https://www.ncbi.nlm.nih.gov/pubmed/32903673
http://dx.doi.org/10.3389/fpls.2020.01215
work_keys_str_mv AT ligen lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT qinbeibei lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT lishuodan lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT yinyue lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT zhaojianhua lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT anwei lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT caoyoulong lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway
AT muzixin lbnrderivednitricoxidedelayslyciumfruitcolorationbytranscriptionallymodifyingflavonoidbiosyntheticpathway