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A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development

Carotenoids are a core plastid component and yet their regulatory function during plastid biogenesis remains enigmatic. A unique carotenoid biosynthesis mutant, carotenoid chloroplast regulation 2 (ccr2), that has no prolamellar body (PLB) and normal PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR) levels,...

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Autores principales: Cazzonelli, Christopher I, Hou, Xin, Alagoz, Yagiz, Rivers, John, Dhami, Namraj, Lee, Jiwon, Marri, Shashikanth, Pogson, Barry J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994220/
https://www.ncbi.nlm.nih.gov/pubmed/32003746
http://dx.doi.org/10.7554/eLife.45310
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author Cazzonelli, Christopher I
Hou, Xin
Alagoz, Yagiz
Rivers, John
Dhami, Namraj
Lee, Jiwon
Marri, Shashikanth
Pogson, Barry J
author_facet Cazzonelli, Christopher I
Hou, Xin
Alagoz, Yagiz
Rivers, John
Dhami, Namraj
Lee, Jiwon
Marri, Shashikanth
Pogson, Barry J
author_sort Cazzonelli, Christopher I
collection PubMed
description Carotenoids are a core plastid component and yet their regulatory function during plastid biogenesis remains enigmatic. A unique carotenoid biosynthesis mutant, carotenoid chloroplast regulation 2 (ccr2), that has no prolamellar body (PLB) and normal PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR) levels, was used to demonstrate a regulatory function for carotenoids and their derivatives under varied dark-light regimes. A forward genetics approach revealed how an epistatic interaction between a ζ-carotene isomerase mutant (ziso-155) and ccr2 blocked the biosynthesis of specific cis-carotenes and restored PLB formation in etioplasts. We attributed this to a novel apocarotenoid retrograde signal, as chemical inhibition of carotenoid cleavage dioxygenase activity restored PLB formation in ccr2 etioplasts during skotomorphogenesis. The apocarotenoid acted in parallel to the repressor of photomorphogenesis, DEETIOLATED1 (DET1), to transcriptionally regulate PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR), PHYTOCHROME INTERACTING FACTOR3 (PIF3) and ELONGATED HYPOCOTYL5 (HY5). The unknown apocarotenoid signal restored POR protein levels and PLB formation in det1, thereby controlling plastid development.
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spelling pubmed-69942202020-02-03 A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development Cazzonelli, Christopher I Hou, Xin Alagoz, Yagiz Rivers, John Dhami, Namraj Lee, Jiwon Marri, Shashikanth Pogson, Barry J eLife Plant Biology Carotenoids are a core plastid component and yet their regulatory function during plastid biogenesis remains enigmatic. A unique carotenoid biosynthesis mutant, carotenoid chloroplast regulation 2 (ccr2), that has no prolamellar body (PLB) and normal PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR) levels, was used to demonstrate a regulatory function for carotenoids and their derivatives under varied dark-light regimes. A forward genetics approach revealed how an epistatic interaction between a ζ-carotene isomerase mutant (ziso-155) and ccr2 blocked the biosynthesis of specific cis-carotenes and restored PLB formation in etioplasts. We attributed this to a novel apocarotenoid retrograde signal, as chemical inhibition of carotenoid cleavage dioxygenase activity restored PLB formation in ccr2 etioplasts during skotomorphogenesis. The apocarotenoid acted in parallel to the repressor of photomorphogenesis, DEETIOLATED1 (DET1), to transcriptionally regulate PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR), PHYTOCHROME INTERACTING FACTOR3 (PIF3) and ELONGATED HYPOCOTYL5 (HY5). The unknown apocarotenoid signal restored POR protein levels and PLB formation in det1, thereby controlling plastid development. eLife Sciences Publications, Ltd 2020-01-31 /pmc/articles/PMC6994220/ /pubmed/32003746 http://dx.doi.org/10.7554/eLife.45310 Text en © 2020, Cazzonelli et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Plant Biology
Cazzonelli, Christopher I
Hou, Xin
Alagoz, Yagiz
Rivers, John
Dhami, Namraj
Lee, Jiwon
Marri, Shashikanth
Pogson, Barry J
A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
title A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
title_full A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
title_fullStr A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
title_full_unstemmed A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
title_short A cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
title_sort cis-carotene derived apocarotenoid regulates etioplast and chloroplast development
topic Plant Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994220/
https://www.ncbi.nlm.nih.gov/pubmed/32003746
http://dx.doi.org/10.7554/eLife.45310
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