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Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria

Phycobilisomes (PBSs), the principal cyanobacterial antenna, are among the most efficient macromolecular structures in nature, and are used for both light harvesting and directed energy transfer to the photosynthetic reaction center. However, under unfavorable conditions, excess excitation energy ne...

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Autores principales: Zhan, Jiao, Steglich, Claudia, Scholz, Ingeborg, Hess, Wolfgang R, Kirilovsky, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136909/
https://www.ncbi.nlm.nih.gov/pubmed/33793852
http://dx.doi.org/10.1093/plcell/koaa030
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author Zhan, Jiao
Steglich, Claudia
Scholz, Ingeborg
Hess, Wolfgang R
Kirilovsky, Diana
author_facet Zhan, Jiao
Steglich, Claudia
Scholz, Ingeborg
Hess, Wolfgang R
Kirilovsky, Diana
author_sort Zhan, Jiao
collection PubMed
description Phycobilisomes (PBSs), the principal cyanobacterial antenna, are among the most efficient macromolecular structures in nature, and are used for both light harvesting and directed energy transfer to the photosynthetic reaction center. However, under unfavorable conditions, excess excitation energy needs to be rapidly dissipated to avoid photodamage. The orange carotenoid protein (OCP) senses light intensity and induces thermal energy dissipation under stress conditions. Hence, its expression must be tightly controlled; however, the molecular mechanism of this regulation remains to be elucidated. Here, we describe the discovery of a posttranscriptional regulatory mechanism in Synechocystis sp. PCC 6803 in which the expression of the operon encoding the allophycocyanin subunits of the PBS is directly and in an inverse fashion linked to the expression of OCP. This regulation is mediated by ApcZ, a small regulatory RNA that is derived from the 3′-end of the tetracistronic apcABC–apcZ operon. ApcZ inhibits ocp translation under stress-free conditions. Under most stress conditions, apc operon transcription decreases and ocp translation increases. Thus, a key operon involved in the collection of light energy is functionally connected to the expression of a protein involved in energy dissipation. Our findings support the view that regulatory RNA networks in bacteria evolve through the functionalization of mRNA 3′-UTRs.
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spelling pubmed-81369092021-05-26 Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria Zhan, Jiao Steglich, Claudia Scholz, Ingeborg Hess, Wolfgang R Kirilovsky, Diana Plant Cell Research Articles Phycobilisomes (PBSs), the principal cyanobacterial antenna, are among the most efficient macromolecular structures in nature, and are used for both light harvesting and directed energy transfer to the photosynthetic reaction center. However, under unfavorable conditions, excess excitation energy needs to be rapidly dissipated to avoid photodamage. The orange carotenoid protein (OCP) senses light intensity and induces thermal energy dissipation under stress conditions. Hence, its expression must be tightly controlled; however, the molecular mechanism of this regulation remains to be elucidated. Here, we describe the discovery of a posttranscriptional regulatory mechanism in Synechocystis sp. PCC 6803 in which the expression of the operon encoding the allophycocyanin subunits of the PBS is directly and in an inverse fashion linked to the expression of OCP. This regulation is mediated by ApcZ, a small regulatory RNA that is derived from the 3′-end of the tetracistronic apcABC–apcZ operon. ApcZ inhibits ocp translation under stress-free conditions. Under most stress conditions, apc operon transcription decreases and ocp translation increases. Thus, a key operon involved in the collection of light energy is functionally connected to the expression of a protein involved in energy dissipation. Our findings support the view that regulatory RNA networks in bacteria evolve through the functionalization of mRNA 3′-UTRs. Oxford University Press 2020-12-14 /pmc/articles/PMC8136909/ /pubmed/33793852 http://dx.doi.org/10.1093/plcell/koaa030 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhan, Jiao
Steglich, Claudia
Scholz, Ingeborg
Hess, Wolfgang R
Kirilovsky, Diana
Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria
title Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria
title_full Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria
title_fullStr Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria
title_full_unstemmed Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria
title_short Inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived sRNA in cyanobacteria
title_sort inverse regulation of light harvesting and photoprotection is mediated by a 3′-end-derived srna in cyanobacteria
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136909/
https://www.ncbi.nlm.nih.gov/pubmed/33793852
http://dx.doi.org/10.1093/plcell/koaa030
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