Regulation by FurC in Anabaena Links the Oxidative Stress Response to Photosynthetic Metabolism

Author:

Sevilla Emma12,Sarasa-Buisan Cristina12,Gonz�lez Andr�s123,Cases Rafael45,Kufryk Galyna6,Peleato M Luisa12,Fillat Mar�a F12ORCID

Affiliation:

1. Departamento de Bioqu�mica y Biolog�a Molecular y Celular, Universidad de Zaragoza, Pedro Cerbuna 12, Zaragoza, Spain

2. Institute for Biocomputation and Physics of Complex Systems, Universidad de Zaragoza, Pedro Cerbuna 12, Zaragoza, Spain

3. Aragon Institute for Health Research (IIS Arag�n), Zaragoza, Spain

4. Instituto de Ciencia de Materiales de Arag�n, Universidad de Zaragoza-CSIC, Zaragoza, Spain

5. Departamento de F�sica de la Materia Condensada, Facultad de Ciencias, Universidad de Zaragoza-CSIC, Zaragoza, Spain

6. College of Science, Engineering and Technology, Grand Canyon University, 3300 W. Camelback Rd, Phoenix, AZ, USA

Abstract

Abstract The FUR (Ferric Uptake Regulator) family in Anabaena sp. PCC 7120 consists of three paralogs named FurA (Fur), FurB (Zur) and FurC (PerR). furC seems to be an essential gene in the filamentous nitrogen-fixing strain Anabaena sp. PCC 7120, suggesting that it plays a fundamental role in this organism. In order to better understand the functions of FurC in Anabaena, the phenotype of a derivative strain that overexpresses this regulator (EB2770FurC) has been characterized. The furC-overexpressing variant presented alterations in growth rate, morphology and ultrastructure, as well as higher sensitivity to peroxide than Anabaena sp. PCC 7120. Interestingly, the overexpression of furC led to reduced photosynthetic O2 evolution, increased respiratory activity, and had a significant influence in the composition and efficiency of both photosystems. Comparative transcriptional analyses, together with electrophoretic mobility shift assays allowed the identification of different genes directly controlled by FurC, and involved in processes not previously related to PerR proteins, such as the cell division gene ftsZ and the major thylakoid membrane protease ftsH. The rise in the transcription of ftsH in EB2770FurC cells correlated with reduced levels of the D1 protein, which is involved in the PSII repair cycle. Deregulation of the oxidative stress response in EB2770FurC cells led to the identification of novel FurC targets involved in the response to H2O2 through different mechanisms. These results, together with the effect of furC overexpression on the composition, stability and efficiency of the photosynthetic machinery of Anabaena, disclose novel links between PerR proteins, cell division and photosynthesis in filamentous cyanobacteria.

Funder

Gobierno de Arag�n

MINECO

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science,Physiology,General Medicine

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