4.7 Article

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

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 72, Issue 21, Pages 7564-7579

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erab416

Keywords

Chloroplasts; CrhR RNA helicase; cyanobacteria; gene expression regulation; photosynthesis; redox regulation; RNA-RNA interaction; small regulatory RNA

Categories

Funding

  1. Baden-Wuerttemberg Foundation [BWST_NCNA_008]
  2. German Research Foundation(DFG) [322977937/GRK2344]
  3. Federal Ministry of Education and Research (BMBF) program RNAProNet [031L0164B]
  4. EU ITN 'Photo.COMM'
  5. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN-201605448]
  6. Department of Biotechnology (DBT) of India [BT/PR13616/BRB/10/774/2010]

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RNA helicases play crucial roles in plants, particularly in response to abiotic stress, development, post-transcriptional gene regulation, and housekeeping functions. These RNA helicases, influenced by cyanobacteria, have diverse molecular targets, with CrhR specifically involved in responding to redox balance in the photosynthetic electron transport chain. The identified interactome of CrhR explains its physiological role and highlights its importance in regulating gene expression in plants.
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.crhR 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.

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