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Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis
BACKGROUND: Transcriptional regulation is a key aspect of environmental stress responses. Heat stress induces transcriptional memory, i.e., sustained induction or enhanced re-induction of transcription, that allows plants to respond more efficiently to a recurrent HS. In light of more frequent tempe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230730/ https://www.ncbi.nlm.nih.gov/pubmed/37254211 http://dx.doi.org/10.1186/s13059-023-02970-5 |
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author | Kappel, Christian Friedrich, Thomas Oberkofler, Vicky Jiang, Li Crawford, Tim Lenhard, Michael Bäurle, Isabel |
author_facet | Kappel, Christian Friedrich, Thomas Oberkofler, Vicky Jiang, Li Crawford, Tim Lenhard, Michael Bäurle, Isabel |
author_sort | Kappel, Christian |
collection | PubMed |
description | BACKGROUND: Transcriptional regulation is a key aspect of environmental stress responses. Heat stress induces transcriptional memory, i.e., sustained induction or enhanced re-induction of transcription, that allows plants to respond more efficiently to a recurrent HS. In light of more frequent temperature extremes due to climate change, improving heat tolerance in crop plants is an important breeding goal. However, not all heat stress-inducible genes show transcriptional memory, and it is unclear what distinguishes memory from non-memory genes. To address this issue and understand the genome and epigenome architecture of transcriptional memory after heat stress, we identify the global target genes of two key memory heat shock transcription factors, HSFA2 and HSFA3, using time course ChIP-seq. RESULTS: HSFA2 and HSFA3 show near identical binding patterns. In vitro and in vivo binding strength is highly correlated, indicating the importance of DNA sequence elements. In particular, genes with transcriptional memory are strongly enriched for a tripartite heat shock element, and are hallmarked by several features: low expression levels in the absence of heat stress, accessible chromatin environment, and heat stress-induced enrichment of H3K4 trimethylation. These results are confirmed by an orthogonal transcriptomic data set using both de novo clustering and an established definition of memory genes. CONCLUSIONS: Our findings provide an integrated view of HSF-dependent transcriptional memory and shed light on its sequence and chromatin determinants, enabling the prediction and engineering of genes with transcriptional memory behavior. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02970-5. |
format | Online Article Text |
id | pubmed-10230730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102307302023-06-01 Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis Kappel, Christian Friedrich, Thomas Oberkofler, Vicky Jiang, Li Crawford, Tim Lenhard, Michael Bäurle, Isabel Genome Biol Research BACKGROUND: Transcriptional regulation is a key aspect of environmental stress responses. Heat stress induces transcriptional memory, i.e., sustained induction or enhanced re-induction of transcription, that allows plants to respond more efficiently to a recurrent HS. In light of more frequent temperature extremes due to climate change, improving heat tolerance in crop plants is an important breeding goal. However, not all heat stress-inducible genes show transcriptional memory, and it is unclear what distinguishes memory from non-memory genes. To address this issue and understand the genome and epigenome architecture of transcriptional memory after heat stress, we identify the global target genes of two key memory heat shock transcription factors, HSFA2 and HSFA3, using time course ChIP-seq. RESULTS: HSFA2 and HSFA3 show near identical binding patterns. In vitro and in vivo binding strength is highly correlated, indicating the importance of DNA sequence elements. In particular, genes with transcriptional memory are strongly enriched for a tripartite heat shock element, and are hallmarked by several features: low expression levels in the absence of heat stress, accessible chromatin environment, and heat stress-induced enrichment of H3K4 trimethylation. These results are confirmed by an orthogonal transcriptomic data set using both de novo clustering and an established definition of memory genes. CONCLUSIONS: Our findings provide an integrated view of HSF-dependent transcriptional memory and shed light on its sequence and chromatin determinants, enabling the prediction and engineering of genes with transcriptional memory behavior. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02970-5. BioMed Central 2023-05-30 /pmc/articles/PMC10230730/ /pubmed/37254211 http://dx.doi.org/10.1186/s13059-023-02970-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kappel, Christian Friedrich, Thomas Oberkofler, Vicky Jiang, Li Crawford, Tim Lenhard, Michael Bäurle, Isabel Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis |
title | Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis |
title_full | Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis |
title_fullStr | Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis |
title_full_unstemmed | Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis |
title_short | Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis |
title_sort | genomic and epigenomic determinants of heat stress-induced transcriptional memory in arabidopsis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230730/ https://www.ncbi.nlm.nih.gov/pubmed/37254211 http://dx.doi.org/10.1186/s13059-023-02970-5 |
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