Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783542834066882560 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7275669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT qiaopengfei transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT bourgaultrichard transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT mohammadimarc transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT matschisusanne transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT philippeglenn transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT smithlaurieg transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT goremichaela transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT molinaisabel transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves AT scanlonmichaelj transcriptomicnetworkanalysesshedlightontheregulationofcuticledevelopmentinmaizeleaves |