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Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton

Plant type III polyketide synthase (PKS) can catalyse the formation of a series of secondary metabolites with different structures and different biological functions; the enzyme plays an important role in plant growth, development and resistance to stress. At present, the PKS gene has been identifie...

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Autores principales: Su, Xueqiang, Sun, Xu, Cheng, Xi, Wang, Yanan, Abdullah, Muhammad, Li, Manli, Li, Dahui, Gao, Junshan, Cai, Yongping, Lin, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667535/
https://www.ncbi.nlm.nih.gov/pubmed/29104824
http://dx.doi.org/10.7717/peerj.3974
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author Su, Xueqiang
Sun, Xu
Cheng, Xi
Wang, Yanan
Abdullah, Muhammad
Li, Manli
Li, Dahui
Gao, Junshan
Cai, Yongping
Lin, Yi
author_facet Su, Xueqiang
Sun, Xu
Cheng, Xi
Wang, Yanan
Abdullah, Muhammad
Li, Manli
Li, Dahui
Gao, Junshan
Cai, Yongping
Lin, Yi
author_sort Su, Xueqiang
collection PubMed
description Plant type III polyketide synthase (PKS) can catalyse the formation of a series of secondary metabolites with different structures and different biological functions; the enzyme plays an important role in plant growth, development and resistance to stress. At present, the PKS gene has been identified and studied in a variety of plants. Here, we identified 11 PKS genes from upland cotton (Gossypium hirsutum) and compared them with 41 PKS genes in Populus tremula, Vitis vinifera, Malus domestica and Arabidopsis thaliana. According to the phylogenetic tree, a total of 52 PKS genes can be divided into four subfamilies (I–IV). The analysis of gene structures and conserved motifs revealed that most of the PKS genes were composed of two exons and one intron and there are two characteristic conserved domains (Chal_sti_synt_N and Chal_sti_synt_C) of the PKS gene family. In our study of the five species, gene duplication was found in addition to Arabidopsis thaliana and we determined that purifying selection has been of great significance in maintaining the function of PKS gene family. From qRT-PCR analysis and a combination of the role of the accumulation of proanthocyanidins (PAs) in brown cotton fibers, we concluded that five PKS genes are candidate genes involved in brown cotton fiber pigment synthesis. These results are important for the further study of brown cotton PKS genes. It not only reveals the relationship between PKS gene family and pigment in brown cotton, but also creates conditions for improving the quality of brown cotton fiber.
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spelling pubmed-56675352017-11-03 Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton Su, Xueqiang Sun, Xu Cheng, Xi Wang, Yanan Abdullah, Muhammad Li, Manli Li, Dahui Gao, Junshan Cai, Yongping Lin, Yi PeerJ Agricultural Science Plant type III polyketide synthase (PKS) can catalyse the formation of a series of secondary metabolites with different structures and different biological functions; the enzyme plays an important role in plant growth, development and resistance to stress. At present, the PKS gene has been identified and studied in a variety of plants. Here, we identified 11 PKS genes from upland cotton (Gossypium hirsutum) and compared them with 41 PKS genes in Populus tremula, Vitis vinifera, Malus domestica and Arabidopsis thaliana. According to the phylogenetic tree, a total of 52 PKS genes can be divided into four subfamilies (I–IV). The analysis of gene structures and conserved motifs revealed that most of the PKS genes were composed of two exons and one intron and there are two characteristic conserved domains (Chal_sti_synt_N and Chal_sti_synt_C) of the PKS gene family. In our study of the five species, gene duplication was found in addition to Arabidopsis thaliana and we determined that purifying selection has been of great significance in maintaining the function of PKS gene family. From qRT-PCR analysis and a combination of the role of the accumulation of proanthocyanidins (PAs) in brown cotton fibers, we concluded that five PKS genes are candidate genes involved in brown cotton fiber pigment synthesis. These results are important for the further study of brown cotton PKS genes. It not only reveals the relationship between PKS gene family and pigment in brown cotton, but also creates conditions for improving the quality of brown cotton fiber. PeerJ Inc. 2017-10-30 /pmc/articles/PMC5667535/ /pubmed/29104824 http://dx.doi.org/10.7717/peerj.3974 Text en ©2017 Su et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Agricultural Science
Su, Xueqiang
Sun, Xu
Cheng, Xi
Wang, Yanan
Abdullah, Muhammad
Li, Manli
Li, Dahui
Gao, Junshan
Cai, Yongping
Lin, Yi
Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton
title Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton
title_full Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton
title_fullStr Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton
title_full_unstemmed Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton
title_short Comparative genomic analysis of the PKS genes in five species and expression analysis in upland cotton
title_sort comparative genomic analysis of the pks genes in five species and expression analysis in upland cotton
topic Agricultural Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667535/
https://www.ncbi.nlm.nih.gov/pubmed/29104824
http://dx.doi.org/10.7717/peerj.3974
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