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Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria

Cytochrome (Cyt) b (559) is a key component of the photosystem II complex (PSII) that is essential for its proper functioning and assembly. Site‐directed mutants of the model cyanobacterium Synechocystis sp. PCC6803 with mutated heme axial ligands of Cyt b (559) have little PSII and are therefore un...

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Autores principales: Chiu, Yi‐Fang, Fu, Han‐Yi, Skotnicová, Petra, Lin, Keng‐Min, Komenda, Josef, Chu, Hsiu‐An
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297868/
https://www.ncbi.nlm.nih.gov/pubmed/34625967
http://dx.doi.org/10.1111/nph.17785
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author Chiu, Yi‐Fang
Fu, Han‐Yi
Skotnicová, Petra
Lin, Keng‐Min
Komenda, Josef
Chu, Hsiu‐An
author_facet Chiu, Yi‐Fang
Fu, Han‐Yi
Skotnicová, Petra
Lin, Keng‐Min
Komenda, Josef
Chu, Hsiu‐An
author_sort Chiu, Yi‐Fang
collection PubMed
description Cytochrome (Cyt) b (559) is a key component of the photosystem II complex (PSII) that is essential for its proper functioning and assembly. Site‐directed mutants of the model cyanobacterium Synechocystis sp. PCC6803 with mutated heme axial ligands of Cyt b (559) have little PSII and are therefore unable to grow photoautotrophically. Here we describe two types of Synechocystis autotrophic transformants that retained the same mutations in Cyt b (559) but are able to accumulate PSII and grow photoautotrophically. Whole‐genome sequencing revealed that all of these autotrophic transformants carried a variable number of tandem repeats (from 5 to 15) of chromosomal segments containing the psbEFLJ operon. RNA‐seq analysis showed greatly increased transcript levels of the psbEFLJ operon in these autotrophic transformants. Multiple copies of the psbEFLJ operon in these transformants were only maintained during autotrophic growth, while its copy numbers gradually decreased under photoheterotrophic conditions. Two‐dimensional PAGE analysis of membrane proteins revealed a strong deficiency in PSII complexes in the Cyt b (559) mutants that was reversed in the autotrophic transformants. These results illustrate how tandem gene amplification restores PSII accumulation and photoautotrophic growth in Cyt b (559) mutants of cyanobacteria, and may serve as an important adaptive mechanism for cyanobacterial survival.
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spelling pubmed-92978682022-07-21 Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria Chiu, Yi‐Fang Fu, Han‐Yi Skotnicová, Petra Lin, Keng‐Min Komenda, Josef Chu, Hsiu‐An New Phytol Research Cytochrome (Cyt) b (559) is a key component of the photosystem II complex (PSII) that is essential for its proper functioning and assembly. Site‐directed mutants of the model cyanobacterium Synechocystis sp. PCC6803 with mutated heme axial ligands of Cyt b (559) have little PSII and are therefore unable to grow photoautotrophically. Here we describe two types of Synechocystis autotrophic transformants that retained the same mutations in Cyt b (559) but are able to accumulate PSII and grow photoautotrophically. Whole‐genome sequencing revealed that all of these autotrophic transformants carried a variable number of tandem repeats (from 5 to 15) of chromosomal segments containing the psbEFLJ operon. RNA‐seq analysis showed greatly increased transcript levels of the psbEFLJ operon in these autotrophic transformants. Multiple copies of the psbEFLJ operon in these transformants were only maintained during autotrophic growth, while its copy numbers gradually decreased under photoheterotrophic conditions. Two‐dimensional PAGE analysis of membrane proteins revealed a strong deficiency in PSII complexes in the Cyt b (559) mutants that was reversed in the autotrophic transformants. These results illustrate how tandem gene amplification restores PSII accumulation and photoautotrophic growth in Cyt b (559) mutants of cyanobacteria, and may serve as an important adaptive mechanism for cyanobacterial survival. John Wiley and Sons Inc. 2021-10-30 2022-01 /pmc/articles/PMC9297868/ /pubmed/34625967 http://dx.doi.org/10.1111/nph.17785 Text en © 2021 The Authors. New Phytologist © 2021 New Phytologist Foundation https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Chiu, Yi‐Fang
Fu, Han‐Yi
Skotnicová, Petra
Lin, Keng‐Min
Komenda, Josef
Chu, Hsiu‐An
Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria
title Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria
title_full Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria
title_fullStr Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria
title_full_unstemmed Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria
title_short Tandem gene amplification restores photosystem II accumulation in cytochrome b (559) mutants of cyanobacteria
title_sort tandem gene amplification restores photosystem ii accumulation in cytochrome b (559) mutants of cyanobacteria
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297868/
https://www.ncbi.nlm.nih.gov/pubmed/34625967
http://dx.doi.org/10.1111/nph.17785
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