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GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis
One of the most dramatic challenges in the life of a plant occurs when the seedling emerges from the soil and exposure to light triggers expression of genes required for establishment of photosynthesis. This process needs to be tightly regulated, as premature accumulation of light‐harvesting protein...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324965/ https://www.ncbi.nlm.nih.gov/pubmed/35322876 http://dx.doi.org/10.1111/nph.18115 |
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author | Hernández‐Verdeja, Tamara Vuorijoki, Linda Jin, Xu Vergara, Alexander Dubreuil, Carole Strand, Åsa |
author_facet | Hernández‐Verdeja, Tamara Vuorijoki, Linda Jin, Xu Vergara, Alexander Dubreuil, Carole Strand, Åsa |
author_sort | Hernández‐Verdeja, Tamara |
collection | PubMed |
description | One of the most dramatic challenges in the life of a plant occurs when the seedling emerges from the soil and exposure to light triggers expression of genes required for establishment of photosynthesis. This process needs to be tightly regulated, as premature accumulation of light‐harvesting proteins and photoreactive Chl precursors causes oxidative damage when the seedling is first exposed to light. Photosynthesis genes are encoded by both nuclear and plastid genomes, and to establish the required level of control, plastid‐to‐nucleus (retrograde) signalling is necessary to ensure correct gene expression. We herein show that a negative GENOMES UNCOUPLED1 (GUN1)‐mediated retrograde signal restricts chloroplast development in darkness and during early light response by regulating the transcription of several critical transcription factors linked to light response, photomorphogenesis, and chloroplast development, and consequently their downstream target genes in Arabidopsis. Thus, the plastids play an essential role during skotomorphogenesis and the early light response, and GUN1 acts as a safeguard during the critical step of seedling emergence from darkness. |
format | Online Article Text |
id | pubmed-9324965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93249652022-07-30 GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis Hernández‐Verdeja, Tamara Vuorijoki, Linda Jin, Xu Vergara, Alexander Dubreuil, Carole Strand, Åsa New Phytol Research One of the most dramatic challenges in the life of a plant occurs when the seedling emerges from the soil and exposure to light triggers expression of genes required for establishment of photosynthesis. This process needs to be tightly regulated, as premature accumulation of light‐harvesting proteins and photoreactive Chl precursors causes oxidative damage when the seedling is first exposed to light. Photosynthesis genes are encoded by both nuclear and plastid genomes, and to establish the required level of control, plastid‐to‐nucleus (retrograde) signalling is necessary to ensure correct gene expression. We herein show that a negative GENOMES UNCOUPLED1 (GUN1)‐mediated retrograde signal restricts chloroplast development in darkness and during early light response by regulating the transcription of several critical transcription factors linked to light response, photomorphogenesis, and chloroplast development, and consequently their downstream target genes in Arabidopsis. Thus, the plastids play an essential role during skotomorphogenesis and the early light response, and GUN1 acts as a safeguard during the critical step of seedling emergence from darkness. John Wiley and Sons Inc. 2022-04-12 2022-07 /pmc/articles/PMC9324965/ /pubmed/35322876 http://dx.doi.org/10.1111/nph.18115 Text en © 2022 The Authors New Phytologist © 2022 New Phytologist Foundation https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Hernández‐Verdeja, Tamara Vuorijoki, Linda Jin, Xu Vergara, Alexander Dubreuil, Carole Strand, Åsa GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis |
title | GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis |
title_full | GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis |
title_fullStr | GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis |
title_full_unstemmed | GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis |
title_short | GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in Arabidopsis |
title_sort | genomes uncoupled1 plays a key role during the de‐etiolation process in arabidopsis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324965/ https://www.ncbi.nlm.nih.gov/pubmed/35322876 http://dx.doi.org/10.1111/nph.18115 |
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