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Characterization of the psbH precursor RNAs reveals a precise endoribonuclease cleavage site in the psbT/psbH intergenic region that is dependent on psbN gene expression

Authors
  • Chevalier, Fabien1, 2, 3, 4
  • Ghulam, Mustafa Malik1, 2, 3, 4
  • Rondet, Damien1, 2, 3, 4
  • Pfannschmidt, Thomas1, 2, 3, 4
  • Merendino, Livia1, 2, 3, 4
  • Lerbs-Mache, Silva1, 2, 3, 4
  • 1 CNRS, Laboratoire Physiologie Cellulaire Végétale, UMR 5168, Grenoble, France , Grenoble (France)
  • 2 Université Grenoble-Alpes, Laboratoire Physiologie Cellulaire Végétale, UMR 5168, Grenoble, France , Grenoble (France)
  • 3 CEA, iRTSV, Laboratoire Physiologie Cellulaire Végétale, UMR 5168, Grenoble, France , Grenoble (France)
  • 4 USC 1359, INRA, Laboratoire Physiologie Cellulaire Végétale, Grenoble, France , Grenoble (France)
Type
Published Article
Journal
Plant Molecular Biology
Publisher
Springer Netherlands
Publication Date
May 27, 2015
Volume
88
Issue
4-5
Pages
357–367
Identifiers
DOI: 10.1007/s11103-015-0325-y
Source
Springer Nature
Keywords
License
Yellow

Abstract

The plastid psbB operon harbours 5 genes, psbB, psbT, psbH, petB and petD. A sixth gene, the psbN gene, is located on the opposite DNA strand in the psbT/psbH intergenic region. Its transcription produces antisense RNA to a large part of the psbB pentacistronic mRNA. We have investigated whether transcription of the psbN gene, i.e. production of antisense RNA, influences psbT/psbH intergenic processing. Results reveal the existence of four different psbH precursor RNAs. Three of them result from processing and one is produced by transcription initiation. One of the processed RNAs is probably created by site-specific RNA cleavage. This RNA is absent in plants where the psbN gene is not transcribed suggesting that cleavage at this site is dependent on the formation of sense/antisense double-stranded RNA. In order to characterize the nuclease that might be responsible for double-stranded RNA cleavage, we analysed csp41a and csp41b knock-out mutants and the corresponding double mutant. Both CSP41 proteins are known to interact physically and CSP41a had been shown to cleave within 3′-untranslated region stem-loop structures, which contain double-stranded RNA, in vitro. We demonstrate that the psbH RNA, that is absent in plants where the psbN gene is not transcribed, is also strongly diminished in all csp41 plants. Altogether, results reveal a site-specific endoribonuclease cleavage event that seems to depend on antisense RNA and might implicate endoribonuclease activity of CSP41a.

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