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The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton

Pigment glands, also known as black glands or gossypol glands, are specific for Gossypium spp. These glands strictly confine large amounts of secondary metabolites to the lysigenous cavity, leading to the glands’ intense colour and providing defence against pests and pathogens. This study performed...

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Autores principales: Gao, Wei, Xu, Fu‐Chun, Long, Lu, Li, Yang, Zhang, Jun‐Li, Chong, Leelyn, Botella, Jose Ramon, Song, Chun‐Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292540/
https://www.ncbi.nlm.nih.gov/pubmed/31883409
http://dx.doi.org/10.1111/pbi.13323
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author Gao, Wei
Xu, Fu‐Chun
Long, Lu
Li, Yang
Zhang, Jun‐Li
Chong, Leelyn
Botella, Jose Ramon
Song, Chun‐Peng
author_facet Gao, Wei
Xu, Fu‐Chun
Long, Lu
Li, Yang
Zhang, Jun‐Li
Chong, Leelyn
Botella, Jose Ramon
Song, Chun‐Peng
author_sort Gao, Wei
collection PubMed
description Pigment glands, also known as black glands or gossypol glands, are specific for Gossypium spp. These glands strictly confine large amounts of secondary metabolites to the lysigenous cavity, leading to the glands’ intense colour and providing defence against pests and pathogens. This study performed a comparative transcriptome analysis of glanded versus glandless cotton cultivars. Twenty‐two transcription factors showed expression patterns associated with pigment glands and were characterized. Phenotypic screening of the genes, via virus‐induced gene silencing, showed an apparent disappearance of pigmented glands after the silencing of a pair of homologous MYB‐encoding genes in the A and D genomes (designated as CGP1). Further study showed that CGP1a encodes an active transcription factor, which is specifically expressed in the gland structure, while CGP1d encodes a non‐functional protein due to a fragment deletion, which causes premature termination. RNAi‐mediated silencing and CRISPR knockout of CGP1 in glanded cotton cultivars generated a glandless‐like phenotype, similar to the dominant glandless mutant Gl(2)(e). Microscopic analysis showed that CGP1 knockout did not affect gland structure or density, but affected gland pigmentation. The levels of gossypol and related terpenoids were significantly decreased in cgp1 mutants, and a number of gossypol biosynthetic genes were strongly down‐regulated. CGP1 is located in the nucleus where it interacts with GoPGF, a critical transcription factor for gland development and gossypol synthesis. Our data suggest that CGP1 and GoPGF form heterodimers to control the synthesis of gossypol and other secondary metabolites in cotton.
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spelling pubmed-72925402020-06-15 The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton Gao, Wei Xu, Fu‐Chun Long, Lu Li, Yang Zhang, Jun‐Li Chong, Leelyn Botella, Jose Ramon Song, Chun‐Peng Plant Biotechnol J Research Articles Pigment glands, also known as black glands or gossypol glands, are specific for Gossypium spp. These glands strictly confine large amounts of secondary metabolites to the lysigenous cavity, leading to the glands’ intense colour and providing defence against pests and pathogens. This study performed a comparative transcriptome analysis of glanded versus glandless cotton cultivars. Twenty‐two transcription factors showed expression patterns associated with pigment glands and were characterized. Phenotypic screening of the genes, via virus‐induced gene silencing, showed an apparent disappearance of pigmented glands after the silencing of a pair of homologous MYB‐encoding genes in the A and D genomes (designated as CGP1). Further study showed that CGP1a encodes an active transcription factor, which is specifically expressed in the gland structure, while CGP1d encodes a non‐functional protein due to a fragment deletion, which causes premature termination. RNAi‐mediated silencing and CRISPR knockout of CGP1 in glanded cotton cultivars generated a glandless‐like phenotype, similar to the dominant glandless mutant Gl(2)(e). Microscopic analysis showed that CGP1 knockout did not affect gland structure or density, but affected gland pigmentation. The levels of gossypol and related terpenoids were significantly decreased in cgp1 mutants, and a number of gossypol biosynthetic genes were strongly down‐regulated. CGP1 is located in the nucleus where it interacts with GoPGF, a critical transcription factor for gland development and gossypol synthesis. Our data suggest that CGP1 and GoPGF form heterodimers to control the synthesis of gossypol and other secondary metabolites in cotton. John Wiley and Sons Inc. 2020-01-21 2020-07 /pmc/articles/PMC7292540/ /pubmed/31883409 http://dx.doi.org/10.1111/pbi.13323 Text en © 2019 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Gao, Wei
Xu, Fu‐Chun
Long, Lu
Li, Yang
Zhang, Jun‐Li
Chong, Leelyn
Botella, Jose Ramon
Song, Chun‐Peng
The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton
title The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton
title_full The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton
title_fullStr The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton
title_full_unstemmed The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton
title_short The gland localized CGP1 controls gland pigmentation and gossypol accumulation in cotton
title_sort gland localized cgp1 controls gland pigmentation and gossypol accumulation in cotton
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292540/
https://www.ncbi.nlm.nih.gov/pubmed/31883409
http://dx.doi.org/10.1111/pbi.13323
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