The temperature-regulated DEAD-box RNA helicase CrhR interactome: autoregulation and photosynthesis-related transcripts

Author:

Migur Anzhela1ORCID,Heyl Florian2,Fuss Janina3,Srikumar Afshan4,Huettel Bruno3ORCID,Steglich Claudia1ORCID,Prakash Jogadhenu S S4ORCID,Reinhardt Richard3ORCID,Backofen Rolf2ORCID,Owttrim George W5ORCID,Hess Wolfgang R1ORCID

Affiliation:

1. Faculty of Biology, University of Freiburg, Schänzlestr. 1, D-79104 Freiburg, Germany

2. Department of Computer Science, University of Freiburg, Georges-Koehler-Allee 106, D-79110 Freiburg, Germany

3. Max Planck-Genome-Centre Cologne, Carl-von-Linné-Weg 10, D-50829 Köln, Germany

4. Department of Biotechnology & Bioinformatics, School of Life Sciences, University of Hyderabad, Hyderabad, India

5. Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9

Abstract

Abstract RNA helicases play crucial roles in RNA biology. In plants, RNA helicases are encoded by large gene families, performing roles in abiotic stress responses, development, the post-transcriptional regulation of gene expression, as well as housekeeping functions. Several of these RNA helicases are targeted to the organelles, the mitochondria and chloroplasts. Cyanobacteria are the direct evolutionary ancestors of plant chloroplasts. The cyanobacterium Synechocystis 6803 encodes a single DEAD-box RNA helicase, CrhR, that is induced by a range of abiotic stresses, including low temperature. Though the ΔcrhR mutant exhibits a severe cold-sensitive phenotype, the physiological function(s) performed by CrhR have not been described. To identify transcripts interacting with CrhR, we performed RNA co-immunoprecipitation with extracts from a Synechocystis crhR deletion mutant expressing the FLAG-tagged native CrhR or a K57A mutated version with an anticipated enhanced RNA binding. The composition of the interactome was strikingly biased towards photosynthesis-associated and redox-controlled transcripts. A transcript highly enriched in all experiments was the crhR mRNA, suggesting an autoregulatory molecular mechanism. The identified interactome explains the described physiological role of CrhR in response to the redox poise of the photosynthetic electron transport chain and characterizes CrhR as an enzyme with a diverse range of transcripts as molecular targets.

Funder

German Research Foundation

Federal Ministry of Education and Research

Natural Sciences and Engineering Research Council of Canada

Department of Biotechnology (DBT) of India

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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