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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,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-6994220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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