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Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes

ARI12 belongs to a family of 16 potential E3 ligases in Arabidopsis and is strongly induced in leaves upon low and high fluence rates (HFR) of UV-B. We have shown that ARI12 is a downstream target of the UV-B receptor, UVR8, and the transcription factors HY5 and HYH under low fluence rates. However...

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Autores principales: Xie, Lisi, Hauser, Marie-Theres
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548860/
https://www.ncbi.nlm.nih.gov/pubmed/22990446
http://dx.doi.org/10.4161/psb.22052
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author Xie, Lisi
Hauser, Marie-Theres
author_facet Xie, Lisi
Hauser, Marie-Theres
author_sort Xie, Lisi
collection PubMed
description ARI12 belongs to a family of 16 potential E3 ligases in Arabidopsis and is strongly induced in leaves upon low and high fluence rates (HFR) of UV-B. We have shown that ARI12 is a downstream target of the UV-B receptor, UVR8, and the transcription factors HY5 and HYH under low fluence rates. However under HFR of broad band UV-B ARI12 expression was still downstream of HY5 and HYH but increased in uvr8 mutants. To determine if other photoreceptors are responsible for the induction of ARI12 we quantified its expression in double mutants of the UV-A and blue light receptors, CRY1/2 and PHOT1/2, and the red light receptors PHYA/B. While the expression of ARI12 was increased in cyr1/2 it was unaffected in phot1/2 and phyA/B. Therefore ARI12 expression is suppressed by UVR8 and cryptochromes, and independent of phototropins and phytochromes A and B upon HFR of broad band UV-B.
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spelling pubmed-35488602013-01-30 Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes Xie, Lisi Hauser, Marie-Theres Plant Signal Behav Short Communication ARI12 belongs to a family of 16 potential E3 ligases in Arabidopsis and is strongly induced in leaves upon low and high fluence rates (HFR) of UV-B. We have shown that ARI12 is a downstream target of the UV-B receptor, UVR8, and the transcription factors HY5 and HYH under low fluence rates. However under HFR of broad band UV-B ARI12 expression was still downstream of HY5 and HYH but increased in uvr8 mutants. To determine if other photoreceptors are responsible for the induction of ARI12 we quantified its expression in double mutants of the UV-A and blue light receptors, CRY1/2 and PHOT1/2, and the red light receptors PHYA/B. While the expression of ARI12 was increased in cyr1/2 it was unaffected in phot1/2 and phyA/B. Therefore ARI12 expression is suppressed by UVR8 and cryptochromes, and independent of phototropins and phytochromes A and B upon HFR of broad band UV-B. Landes Bioscience 2012-11-01 /pmc/articles/PMC3548860/ /pubmed/22990446 http://dx.doi.org/10.4161/psb.22052 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Short Communication
Xie, Lisi
Hauser, Marie-Theres
Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes
title Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes
title_full Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes
title_fullStr Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes
title_full_unstemmed Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes
title_short Induction of ARI12 upon broad band UV-B radiation is suppressed by UVR8 and cryptochromes
title_sort induction of ari12 upon broad band uv-b radiation is suppressed by uvr8 and cryptochromes
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548860/
https://www.ncbi.nlm.nih.gov/pubmed/22990446
http://dx.doi.org/10.4161/psb.22052
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