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Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns

The distribution of type I and II chalcone isomerases (CHIs) in plants is highly family specific. We have previously reported that ancient land plants, such as the liverworts and Selaginella moellendorffii, harbor type II CHIs. To better understand the function and evolution of CHI-fold proteins, tr...

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Autores principales: Ni, Rong, Zhu, Ting-Ting, Zhang, Xiao-Shuang, Wang, Piao-Yi, Sun, Chun-Jing, Qiao, Ya-Nan, Lou, Hong-Xiang, Cheng, Ai-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913697/
https://www.ncbi.nlm.nih.gov/pubmed/31557291
http://dx.doi.org/10.1093/jxb/erz425
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author Ni, Rong
Zhu, Ting-Ting
Zhang, Xiao-Shuang
Wang, Piao-Yi
Sun, Chun-Jing
Qiao, Ya-Nan
Lou, Hong-Xiang
Cheng, Ai-Xia
author_facet Ni, Rong
Zhu, Ting-Ting
Zhang, Xiao-Shuang
Wang, Piao-Yi
Sun, Chun-Jing
Qiao, Ya-Nan
Lou, Hong-Xiang
Cheng, Ai-Xia
author_sort Ni, Rong
collection PubMed
description The distribution of type I and II chalcone isomerases (CHIs) in plants is highly family specific. We have previously reported that ancient land plants, such as the liverworts and Selaginella moellendorffii, harbor type II CHIs. To better understand the function and evolution of CHI-fold proteins, transcriptomic data obtained from 52 pteridophyte species were subjected to sequence alignment and phylogenetic analysis. The residues determining type I/II CHI identity in the pteridophyte CHIs were identical to those of type I CHIs. The enzymatic characterization of a sample of 24 CHIs, representing all the key pteridophyte lineages, demonstrated that 19 of them were type I enzymes and that five exhibited some type II activity due to an amino acid mutation. Two pteridophyte chalcone synthases (CHSs) were also characterized, and a type IV CHI (CHIL) was demonstrated to interact physically with CHSs and CHI, and to increase CHS activity by decreasing derailment products, thus enhancing flavonoid production. These findings suggest that the emergence of type I CHIs may have coincided with the divergence of the pteridophytes. This study deepens our understanding of the molecular mechanism of CHIL as an enhancer in the flavonoid biosynthesis pathway.
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spelling pubmed-69136972019-12-19 Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns Ni, Rong Zhu, Ting-Ting Zhang, Xiao-Shuang Wang, Piao-Yi Sun, Chun-Jing Qiao, Ya-Nan Lou, Hong-Xiang Cheng, Ai-Xia J Exp Bot Research Papers The distribution of type I and II chalcone isomerases (CHIs) in plants is highly family specific. We have previously reported that ancient land plants, such as the liverworts and Selaginella moellendorffii, harbor type II CHIs. To better understand the function and evolution of CHI-fold proteins, transcriptomic data obtained from 52 pteridophyte species were subjected to sequence alignment and phylogenetic analysis. The residues determining type I/II CHI identity in the pteridophyte CHIs were identical to those of type I CHIs. The enzymatic characterization of a sample of 24 CHIs, representing all the key pteridophyte lineages, demonstrated that 19 of them were type I enzymes and that five exhibited some type II activity due to an amino acid mutation. Two pteridophyte chalcone synthases (CHSs) were also characterized, and a type IV CHI (CHIL) was demonstrated to interact physically with CHSs and CHI, and to increase CHS activity by decreasing derailment products, thus enhancing flavonoid production. These findings suggest that the emergence of type I CHIs may have coincided with the divergence of the pteridophytes. This study deepens our understanding of the molecular mechanism of CHIL as an enhancer in the flavonoid biosynthesis pathway. Oxford University Press 2020-01-01 2019-09-26 /pmc/articles/PMC6913697/ /pubmed/31557291 http://dx.doi.org/10.1093/jxb/erz425 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Papers
Ni, Rong
Zhu, Ting-Ting
Zhang, Xiao-Shuang
Wang, Piao-Yi
Sun, Chun-Jing
Qiao, Ya-Nan
Lou, Hong-Xiang
Cheng, Ai-Xia
Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
title Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
title_full Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
title_fullStr Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
title_full_unstemmed Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
title_short Identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
title_sort identification and evolutionary analysis of chalcone isomerase-fold proteins in ferns
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913697/
https://www.ncbi.nlm.nih.gov/pubmed/31557291
http://dx.doi.org/10.1093/jxb/erz425
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