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The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway
In plants, an elevation in ambient temperature induces adaptive morphological changes including elongated hypocotyls, which is predominantly regulated by a bHLH transcription factor, PIF4. Although PIF4 is expressed in all aerial tissues including the epidermis, mesophyll, and vascular bundle, its t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044213/ https://www.ncbi.nlm.nih.gov/pubmed/32103019 http://dx.doi.org/10.1038/s41467-020-14905-w |
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author | Kim, Sara Hwang, Geonhee Kim, Soohwan Thi, Thom Nguyen Kim, Hanim Jeong, Jinkil Kim, Jaewook Kim, Jungmook Choi, Giltsu Oh, Eunkyoo |
author_facet | Kim, Sara Hwang, Geonhee Kim, Soohwan Thi, Thom Nguyen Kim, Hanim Jeong, Jinkil Kim, Jaewook Kim, Jungmook Choi, Giltsu Oh, Eunkyoo |
author_sort | Kim, Sara |
collection | PubMed |
description | In plants, an elevation in ambient temperature induces adaptive morphological changes including elongated hypocotyls, which is predominantly regulated by a bHLH transcription factor, PIF4. Although PIF4 is expressed in all aerial tissues including the epidermis, mesophyll, and vascular bundle, its tissue-specific functions in thermomorphogenesis are not known. Here, we show that epidermis-specific expression of PIF4 induces constitutive long hypocotyls, while vasculature-specific expression of PIF4 has no effect on hypocotyl growth. RNA-Seq and qRT-PCR analyses reveal that auxin-responsive genes and growth-related genes are highly activated by epidermal, but not by vascular, PIF4. Additionally, inactivation of epidermal PIF4 or auxin signaling, and overexpression of epidermal phyB suppresses thermoresponsive growth, indicating that epidermal PIF4-auxin pathways are essential for the temperature responses. Further, we show that high temperatures increase both epidermal PIF4 transcription and the epidermal PIF4 DNA-binding ability. Taken together, our study demonstrates that the epidermis regulates thermoresponsive growth through the phyB-PIF4-auxin pathway. |
format | Online Article Text |
id | pubmed-7044213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70442132020-03-04 The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway Kim, Sara Hwang, Geonhee Kim, Soohwan Thi, Thom Nguyen Kim, Hanim Jeong, Jinkil Kim, Jaewook Kim, Jungmook Choi, Giltsu Oh, Eunkyoo Nat Commun Article In plants, an elevation in ambient temperature induces adaptive morphological changes including elongated hypocotyls, which is predominantly regulated by a bHLH transcription factor, PIF4. Although PIF4 is expressed in all aerial tissues including the epidermis, mesophyll, and vascular bundle, its tissue-specific functions in thermomorphogenesis are not known. Here, we show that epidermis-specific expression of PIF4 induces constitutive long hypocotyls, while vasculature-specific expression of PIF4 has no effect on hypocotyl growth. RNA-Seq and qRT-PCR analyses reveal that auxin-responsive genes and growth-related genes are highly activated by epidermal, but not by vascular, PIF4. Additionally, inactivation of epidermal PIF4 or auxin signaling, and overexpression of epidermal phyB suppresses thermoresponsive growth, indicating that epidermal PIF4-auxin pathways are essential for the temperature responses. Further, we show that high temperatures increase both epidermal PIF4 transcription and the epidermal PIF4 DNA-binding ability. Taken together, our study demonstrates that the epidermis regulates thermoresponsive growth through the phyB-PIF4-auxin pathway. Nature Publishing Group UK 2020-02-26 /pmc/articles/PMC7044213/ /pubmed/32103019 http://dx.doi.org/10.1038/s41467-020-14905-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Sara Hwang, Geonhee Kim, Soohwan Thi, Thom Nguyen Kim, Hanim Jeong, Jinkil Kim, Jaewook Kim, Jungmook Choi, Giltsu Oh, Eunkyoo The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway |
title | The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway |
title_full | The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway |
title_fullStr | The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway |
title_full_unstemmed | The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway |
title_short | The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway |
title_sort | epidermis coordinates thermoresponsive growth through the phyb-pif4-auxin pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044213/ https://www.ncbi.nlm.nih.gov/pubmed/32103019 http://dx.doi.org/10.1038/s41467-020-14905-w |
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