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  • New Phytologist - 2022 - Hernndez‐Verdeja - GENOMES UNCOUPLED1 plays a key role during the de‐etiolation process in

    Rights statement: This is the peer reviewed version of the following article: Hernández-Verdeja, T., Vuorijoki, L., Jin, X., Vergara, A., Dubreuil, C. and Strand, Å. (2022), GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. New Phytol, 235: 188-203. doi:10.1111/nph.18115 which has been published in final form at https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.18115 This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.

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GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. / Hernandez-Verdeja, Tamara; Vuorijoki, Linda; Jin, Xu et al.
In: New Phytologist, Vol. 235, No. 1, 31.07.2022, p. 188-203.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Hernandez-Verdeja, T, Vuorijoki, L, Jin, X, Vergara, A, Dubreuil, C & Strand, A 2022, 'GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis', New Phytologist, vol. 235, no. 1, pp. 188-203. https://doi.org/10.1111/nph.18115

APA

Hernandez-Verdeja, T., Vuorijoki, L., Jin, X., Vergara, A., Dubreuil, C., & Strand, A. (2022). GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. New Phytologist, 235(1), 188-203. https://doi.org/10.1111/nph.18115

Vancouver

Hernandez-Verdeja T, Vuorijoki L, Jin X, Vergara A, Dubreuil C, Strand A. GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. New Phytologist. 2022 Jul 31;235(1):188-203. Epub 2022 Apr 12. doi: 10.1111/nph.18115

Author

Hernandez-Verdeja, Tamara ; Vuorijoki, Linda ; Jin, Xu et al. / GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. In: New Phytologist. 2022 ; Vol. 235, No. 1. pp. 188-203.

Bibtex

@article{3efa3737f222401f9fde78e5b46e1149,
title = "GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis",
abstract = "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 chlorophyll precursors cause 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 GUN1-mediated retrograde signal restricts chloroplast development in darkness and during early light response by regulating the transcription of several critical TFs 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.",
keywords = "chloroplast, greening, GUN1, light signalling, plastid retrograde signalling, transcriptional regulation",
author = "Tamara Hernandez-Verdeja and Linda Vuorijoki and Xu Jin and Alexander Vergara and Carole Dubreuil and Asa Strand",
note = "This is the peer reviewed version of the following article: Hern{\'a}ndez-Verdeja, T., Vuorijoki, L., Jin, X., Vergara, A., Dubreuil, C. and Strand, {\AA}. (2022), GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. New Phytol, 235: 188-203. doi:10.1111/nph.18115 which has been published in final form at https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.18115 This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving. ",
year = "2022",
month = jul,
day = "31",
doi = "10.1111/nph.18115",
language = "English",
volume = "235",
pages = "188--203",
journal = "New Phytologist",
issn = "0028-646X",
publisher = "Wiley",
number = "1",

}

RIS

TY - JOUR

T1 - GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis

AU - Hernandez-Verdeja, Tamara

AU - Vuorijoki, Linda

AU - Jin, Xu

AU - Vergara, Alexander

AU - Dubreuil, Carole

AU - Strand, Asa

N1 - This is the peer reviewed version of the following article: Hernández-Verdeja, T., Vuorijoki, L., Jin, X., Vergara, A., Dubreuil, C. and Strand, Å. (2022), GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis. New Phytol, 235: 188-203. doi:10.1111/nph.18115 which has been published in final form at https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.18115 This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.

PY - 2022/7/31

Y1 - 2022/7/31

N2 - 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 chlorophyll precursors cause 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 GUN1-mediated retrograde signal restricts chloroplast development in darkness and during early light response by regulating the transcription of several critical TFs 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.

AB - 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 chlorophyll precursors cause 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 GUN1-mediated retrograde signal restricts chloroplast development in darkness and during early light response by regulating the transcription of several critical TFs 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.

KW - chloroplast

KW - greening

KW - GUN1

KW - light signalling

KW - plastid retrograde signalling

KW - transcriptional regulation

U2 - 10.1111/nph.18115

DO - 10.1111/nph.18115

M3 - Journal article

VL - 235

SP - 188

EP - 203

JO - New Phytologist

JF - New Phytologist

SN - 0028-646X

IS - 1

ER -