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An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis
Plant growth and development are acutely sensitive to high ambient temperature caused in part due to climate change. However, the mechanism of high ambient temperature signaling is not well defined. Here, we show that HECATEs (HEC1 and HEC2), two helix-loop-helix transcription factors, inhibit therm...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195427/ https://www.ncbi.nlm.nih.gov/pubmed/34061850 http://dx.doi.org/10.1371/journal.pgen.1009595 |
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author | Lee, Sanghwa Zhu, Ling Huq, Enamul |
author_facet | Lee, Sanghwa Zhu, Ling Huq, Enamul |
author_sort | Lee, Sanghwa |
collection | PubMed |
description | Plant growth and development are acutely sensitive to high ambient temperature caused in part due to climate change. However, the mechanism of high ambient temperature signaling is not well defined. Here, we show that HECATEs (HEC1 and HEC2), two helix-loop-helix transcription factors, inhibit thermomorphogenesis. While the expression of HEC1 and HEC2 is increased and HEC2 protein is stabilized at high ambient temperature, hec1hec2 double mutant showed exaggerated thermomorphogenesis. Analyses of the four PHYTOCHROME INTERACTING FACTOR (PIF1, PIF3, PIF4 and PIF5) mutants and overexpression lines showed that they all contribute to promote thermomorphogenesis. Furthermore, genetic analysis showed that pifQ is epistatic to hec1hec2. HECs and PIFs oppositely control the expression of many genes in response to high ambient temperature. PIFs activate the expression of HECs in response to high ambient temperature. HEC2 in turn interacts with PIF4 both in yeast and in vivo. In the absence of HECs, PIF4 binding to its own promoter as well as the target gene promoters was enhanced, indicating that HECs control PIF4 activity via heterodimerization. Overall, these data suggest that PIF4-HEC forms an autoregulatory composite negative feedback loop that controls growth genes to modulate thermomorphogenesis. |
format | Online Article Text |
id | pubmed-8195427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81954272021-06-21 An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis Lee, Sanghwa Zhu, Ling Huq, Enamul PLoS Genet Research Article Plant growth and development are acutely sensitive to high ambient temperature caused in part due to climate change. However, the mechanism of high ambient temperature signaling is not well defined. Here, we show that HECATEs (HEC1 and HEC2), two helix-loop-helix transcription factors, inhibit thermomorphogenesis. While the expression of HEC1 and HEC2 is increased and HEC2 protein is stabilized at high ambient temperature, hec1hec2 double mutant showed exaggerated thermomorphogenesis. Analyses of the four PHYTOCHROME INTERACTING FACTOR (PIF1, PIF3, PIF4 and PIF5) mutants and overexpression lines showed that they all contribute to promote thermomorphogenesis. Furthermore, genetic analysis showed that pifQ is epistatic to hec1hec2. HECs and PIFs oppositely control the expression of many genes in response to high ambient temperature. PIFs activate the expression of HECs in response to high ambient temperature. HEC2 in turn interacts with PIF4 both in yeast and in vivo. In the absence of HECs, PIF4 binding to its own promoter as well as the target gene promoters was enhanced, indicating that HECs control PIF4 activity via heterodimerization. Overall, these data suggest that PIF4-HEC forms an autoregulatory composite negative feedback loop that controls growth genes to modulate thermomorphogenesis. Public Library of Science 2021-06-01 /pmc/articles/PMC8195427/ /pubmed/34061850 http://dx.doi.org/10.1371/journal.pgen.1009595 Text en © 2021 Lee et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, Sanghwa Zhu, Ling Huq, Enamul An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis |
title | An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis |
title_full | An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis |
title_fullStr | An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis |
title_full_unstemmed | An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis |
title_short | An autoregulatory negative feedback loop controls thermomorphogenesis in Arabidopsis |
title_sort | autoregulatory negative feedback loop controls thermomorphogenesis in arabidopsis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195427/ https://www.ncbi.nlm.nih.gov/pubmed/34061850 http://dx.doi.org/10.1371/journal.pgen.1009595 |
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