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Genetic and evolution analysis of extrafloral nectary in cotton
Extrafloral nectaries are a defence trait that plays important roles in plant–animal interactions. Gossypium species are characterized by cellular grooves in leaf midribs that secret large amounts of nectar. Here, with a panel of 215 G. arboreum accessions, we compared extrafloral nectaries to necta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540171/ https://www.ncbi.nlm.nih.gov/pubmed/32096298 http://dx.doi.org/10.1111/pbi.13366 |
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author | Hu, Wei Qin, Wenqiang Jin, Yuying Wang, Peng Yan, Qingdi Li, Fuguang Yang, Zhaoen |
author_facet | Hu, Wei Qin, Wenqiang Jin, Yuying Wang, Peng Yan, Qingdi Li, Fuguang Yang, Zhaoen |
author_sort | Hu, Wei |
collection | PubMed |
description | Extrafloral nectaries are a defence trait that plays important roles in plant–animal interactions. Gossypium species are characterized by cellular grooves in leaf midribs that secret large amounts of nectar. Here, with a panel of 215 G. arboreum accessions, we compared extrafloral nectaries to nectariless accessions to identify a region of Chr12 that showed strong differentiation and overlapped with signals from GWAS of nectaries. Fine mapping of an F(2) population identified GaNEC1, encoding a PB1 domain‐containing protein, as a positive regulator of nectary formation. An InDel, encoding a five amino acid deletion, together with a nonsynonymous substitution, was predicted to cause 3D structural changes in GaNEC1 protein that could confer the nectariless phenotype. mRNA‐Seq analysis showed that JA‐related genes are up‐regulated and cell wall‐related genes are down‐regulated in the nectary. Silencing of GaNEC1 led to a smaller size of foliar nectary phenotype. Metabolomics analysis identified more than 400 metabolites in nectar, including expected saccharides and amino acids. The identification of GaNEC1 helps establish the network regulating nectary formation and nectar secretion, and has implications for understanding the production of secondary metabolites in nectar. Our results will deepen our understanding of plant–mutualism co‐evolution and interactions, and will enable utilization of a plant defence trait in cotton breeding efforts. |
format | Online Article Text |
id | pubmed-7540171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75401712020-10-09 Genetic and evolution analysis of extrafloral nectary in cotton Hu, Wei Qin, Wenqiang Jin, Yuying Wang, Peng Yan, Qingdi Li, Fuguang Yang, Zhaoen Plant Biotechnol J Research Articles Extrafloral nectaries are a defence trait that plays important roles in plant–animal interactions. Gossypium species are characterized by cellular grooves in leaf midribs that secret large amounts of nectar. Here, with a panel of 215 G. arboreum accessions, we compared extrafloral nectaries to nectariless accessions to identify a region of Chr12 that showed strong differentiation and overlapped with signals from GWAS of nectaries. Fine mapping of an F(2) population identified GaNEC1, encoding a PB1 domain‐containing protein, as a positive regulator of nectary formation. An InDel, encoding a five amino acid deletion, together with a nonsynonymous substitution, was predicted to cause 3D structural changes in GaNEC1 protein that could confer the nectariless phenotype. mRNA‐Seq analysis showed that JA‐related genes are up‐regulated and cell wall‐related genes are down‐regulated in the nectary. Silencing of GaNEC1 led to a smaller size of foliar nectary phenotype. Metabolomics analysis identified more than 400 metabolites in nectar, including expected saccharides and amino acids. The identification of GaNEC1 helps establish the network regulating nectary formation and nectar secretion, and has implications for understanding the production of secondary metabolites in nectar. Our results will deepen our understanding of plant–mutualism co‐evolution and interactions, and will enable utilization of a plant defence trait in cotton breeding efforts. John Wiley and Sons Inc. 2020-03-10 2020-10 /pmc/articles/PMC7540171/ /pubmed/32096298 http://dx.doi.org/10.1111/pbi.13366 Text en © 2020 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 Hu, Wei Qin, Wenqiang Jin, Yuying Wang, Peng Yan, Qingdi Li, Fuguang Yang, Zhaoen Genetic and evolution analysis of extrafloral nectary in cotton |
title | Genetic and evolution analysis of extrafloral nectary in cotton |
title_full | Genetic and evolution analysis of extrafloral nectary in cotton |
title_fullStr | Genetic and evolution analysis of extrafloral nectary in cotton |
title_full_unstemmed | Genetic and evolution analysis of extrafloral nectary in cotton |
title_short | Genetic and evolution analysis of extrafloral nectary in cotton |
title_sort | genetic and evolution analysis of extrafloral nectary in cotton |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540171/ https://www.ncbi.nlm.nih.gov/pubmed/32096298 http://dx.doi.org/10.1111/pbi.13366 |
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