Cargando…
Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6
Plants ‘memorize’ stressful events and protect themselves from future, often more severe, stresses. To maximize growth after stress, plants ‘reset’ or ‘forget’ memories of stressful situations, which requires an intricate balance between stress memory formation and the degree of forgetfulness. HEAT...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578354/ https://www.ncbi.nlm.nih.gov/pubmed/35705109 http://dx.doi.org/10.1093/jxb/erac257 |
_version_ | 1784811954872778752 |
---|---|
author | Sedaghatmehr, Mastoureh Stüwe, Benno Mueller-Roeber, Bernd Balazadeh, Salma |
author_facet | Sedaghatmehr, Mastoureh Stüwe, Benno Mueller-Roeber, Bernd Balazadeh, Salma |
author_sort | Sedaghatmehr, Mastoureh |
collection | PubMed |
description | Plants ‘memorize’ stressful events and protect themselves from future, often more severe, stresses. To maximize growth after stress, plants ‘reset’ or ‘forget’ memories of stressful situations, which requires an intricate balance between stress memory formation and the degree of forgetfulness. HEAT SHOCK PROTEIN 21 (HSP21) encodes a small heat shock protein in plastids of Arabidopsis thaliana. HSP21 functions as a key component of thermomemory, which requires a sustained elevated level of HSP21 during recovery from heat stress. A heat-induced metalloprotease, filamentation temperature-sensitive H6 (FtsH6), degrades HSP21 to its pre-stress abundance, thereby resetting memory during the recovery phase. The transcription factor heat shock factor A2 (HSFA2) activates downstream genes essential for mounting thermomemory, acting as a positive regulator in the process. Here, using a yeast one-hybrid screen, we identify HSFA2 as an upstream transactivator of the resetting element FtsH6. Constitutive and inducible overexpression of HSFA2 increases expression of FtsH6, whereas it is drastically reduced in the hsfa2 knockout mutant. Chromatin immunoprecipitation reveals in planta binding of HSFA2 to the FtsH6 promoter. Importantly, overexpression of HSFA2 improves thermomemory more profoundly in ftsh6 than wild-type plants. Thus, by activating both memory-supporting and memory-resetting genes, HSFA2 acts as a cellular homeostasis factor during thermomemory. |
format | Online Article Text |
id | pubmed-9578354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95783542022-10-19 Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 Sedaghatmehr, Mastoureh Stüwe, Benno Mueller-Roeber, Bernd Balazadeh, Salma J Exp Bot Research Papers Plants ‘memorize’ stressful events and protect themselves from future, often more severe, stresses. To maximize growth after stress, plants ‘reset’ or ‘forget’ memories of stressful situations, which requires an intricate balance between stress memory formation and the degree of forgetfulness. HEAT SHOCK PROTEIN 21 (HSP21) encodes a small heat shock protein in plastids of Arabidopsis thaliana. HSP21 functions as a key component of thermomemory, which requires a sustained elevated level of HSP21 during recovery from heat stress. A heat-induced metalloprotease, filamentation temperature-sensitive H6 (FtsH6), degrades HSP21 to its pre-stress abundance, thereby resetting memory during the recovery phase. The transcription factor heat shock factor A2 (HSFA2) activates downstream genes essential for mounting thermomemory, acting as a positive regulator in the process. Here, using a yeast one-hybrid screen, we identify HSFA2 as an upstream transactivator of the resetting element FtsH6. Constitutive and inducible overexpression of HSFA2 increases expression of FtsH6, whereas it is drastically reduced in the hsfa2 knockout mutant. Chromatin immunoprecipitation reveals in planta binding of HSFA2 to the FtsH6 promoter. Importantly, overexpression of HSFA2 improves thermomemory more profoundly in ftsh6 than wild-type plants. Thus, by activating both memory-supporting and memory-resetting genes, HSFA2 acts as a cellular homeostasis factor during thermomemory. Oxford University Press 2022-06-15 /pmc/articles/PMC9578354/ /pubmed/35705109 http://dx.doi.org/10.1093/jxb/erac257 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Sedaghatmehr, Mastoureh Stüwe, Benno Mueller-Roeber, Bernd Balazadeh, Salma Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 |
title | Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 |
title_full | Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 |
title_fullStr | Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 |
title_full_unstemmed | Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 |
title_short | Heat shock factor HSFA2 fine-tunes resetting of thermomemory via plastidic metalloprotease FtsH6 |
title_sort | heat shock factor hsfa2 fine-tunes resetting of thermomemory via plastidic metalloprotease ftsh6 |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578354/ https://www.ncbi.nlm.nih.gov/pubmed/35705109 http://dx.doi.org/10.1093/jxb/erac257 |
work_keys_str_mv | AT sedaghatmehrmastoureh heatshockfactorhsfa2finetunesresettingofthermomemoryviaplastidicmetalloproteaseftsh6 AT stuwebenno heatshockfactorhsfa2finetunesresettingofthermomemoryviaplastidicmetalloproteaseftsh6 AT muellerroeberbernd heatshockfactorhsfa2finetunesresettingofthermomemoryviaplastidicmetalloproteaseftsh6 AT balazadehsalma heatshockfactorhsfa2finetunesresettingofthermomemoryviaplastidicmetalloproteaseftsh6 |