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Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves

Plant cuticles are composed of wax and cutin and evolved in the land plants as a hydrophobic boundary that reduces water loss from the plant epidermis. The expanding maize adult leaf displays a dynamic, proximodistal gradient of cuticle development, from the leaf base to the tip. Laser microdissecti...

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Autores principales: Qiao, Pengfei, Bourgault, Richard, Mohammadi, Marc, Matschi, Susanne, Philippe, Glenn, Smith, Laurie G., Gore, Michael A., Molina, Isabel, Scanlon, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275669/
https://www.ncbi.nlm.nih.gov/pubmed/32424100
http://dx.doi.org/10.1073/pnas.2004945117
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author Qiao, Pengfei
Bourgault, Richard
Mohammadi, Marc
Matschi, Susanne
Philippe, Glenn
Smith, Laurie G.
Gore, Michael A.
Molina, Isabel
Scanlon, Michael J.
author_facet Qiao, Pengfei
Bourgault, Richard
Mohammadi, Marc
Matschi, Susanne
Philippe, Glenn
Smith, Laurie G.
Gore, Michael A.
Molina, Isabel
Scanlon, Michael J.
author_sort Qiao, Pengfei
collection PubMed
description Plant cuticles are composed of wax and cutin and evolved in the land plants as a hydrophobic boundary that reduces water loss from the plant epidermis. The expanding maize adult leaf displays a dynamic, proximodistal gradient of cuticle development, from the leaf base to the tip. Laser microdissection RNA Sequencing (LM-RNAseq) was performed along this proximodistal gradient, and complementary network analyses identified potential regulators of cuticle biosynthesis and deposition. A weighted gene coexpression network (WGCN) analysis suggested a previously undescribed function for PHYTOCHROME-mediated light signaling during the regulation of cuticular wax deposition. Genetic analyses reveal that phyB1 phyB2 double mutants of maize exhibit abnormal cuticle composition, supporting the predictions of our coexpression analysis. Reverse genetic analyses also show that phy mutants of the moss Physcomitrella patens exhibit abnormal cuticle composition, suggesting an ancestral role for PHYTOCHROME-mediated, light-stimulated regulation of cuticle development during plant evolution.
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spelling pubmed-72756692020-06-11 Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves Qiao, Pengfei Bourgault, Richard Mohammadi, Marc Matschi, Susanne Philippe, Glenn Smith, Laurie G. Gore, Michael A. Molina, Isabel Scanlon, Michael J. Proc Natl Acad Sci U S A Biological Sciences Plant cuticles are composed of wax and cutin and evolved in the land plants as a hydrophobic boundary that reduces water loss from the plant epidermis. The expanding maize adult leaf displays a dynamic, proximodistal gradient of cuticle development, from the leaf base to the tip. Laser microdissection RNA Sequencing (LM-RNAseq) was performed along this proximodistal gradient, and complementary network analyses identified potential regulators of cuticle biosynthesis and deposition. A weighted gene coexpression network (WGCN) analysis suggested a previously undescribed function for PHYTOCHROME-mediated light signaling during the regulation of cuticular wax deposition. Genetic analyses reveal that phyB1 phyB2 double mutants of maize exhibit abnormal cuticle composition, supporting the predictions of our coexpression analysis. Reverse genetic analyses also show that phy mutants of the moss Physcomitrella patens exhibit abnormal cuticle composition, suggesting an ancestral role for PHYTOCHROME-mediated, light-stimulated regulation of cuticle development during plant evolution. National Academy of Sciences 2020-06-02 2020-05-18 /pmc/articles/PMC7275669/ /pubmed/32424100 http://dx.doi.org/10.1073/pnas.2004945117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Qiao, Pengfei
Bourgault, Richard
Mohammadi, Marc
Matschi, Susanne
Philippe, Glenn
Smith, Laurie G.
Gore, Michael A.
Molina, Isabel
Scanlon, Michael J.
Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
title Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
title_full Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
title_fullStr Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
title_full_unstemmed Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
title_short Transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
title_sort transcriptomic network analyses shed light on the regulation of cuticle development in maize leaves
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275669/
https://www.ncbi.nlm.nih.gov/pubmed/32424100
http://dx.doi.org/10.1073/pnas.2004945117
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