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

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Fabien Chevalier
  • Mustafa Malik Ghulam
  • Damien Rondet
  • Thomas Pfannschmidt
  • Livia Merendino
  • Silva Lerbs-Mache

Organisationseinheiten

Externe Organisationen

  • Laboratoire Physiologie Cellulaire & Végétale
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)357-67
Seitenumfang11
FachzeitschriftPlant molecular biology
Jahrgang88
Ausgabenummer4-5
PublikationsstatusVeröffentlicht - Juli 2015

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.

Zitieren

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. / Chevalier, Fabien; Ghulam, Mustafa Malik; Rondet, Damien et al.
in: Plant molecular biology, Jahrgang 88, Nr. 4-5, 07.2015, S. 357-67.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Download
@article{6a4b49dfc2084c1a9782b2661cb7c3e1,
title = "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",
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. ",
keywords = "Arabidopsis/genetics, Arabidopsis Proteins/genetics, Base Sequence, Binding Sites/genetics, Chloroplasts/genetics, DNA, Intergenic, Endoribonucleases/genetics, Gene Expression, Genes, Plant, Molecular Sequence Data, Mutation, Phosphoproteins/genetics, Photosystem II Protein Complex/genetics, Plants, Genetically Modified, RNA Precursors/genetics, RNA Processing, Post-Transcriptional, RNA, Antisense/genetics, RNA, Plant/genetics",
author = "Fabien Chevalier and Ghulam, {Mustafa Malik} and Damien Rondet and Thomas Pfannschmidt and Livia Merendino and Silva Lerbs-Mache",
year = "2015",
month = jul,
doi = "10.1007/s11103-015-0325-y",
language = "English",
volume = "88",
pages = "357--67",
journal = "Plant molecular biology",
issn = "0167-4412",
publisher = "Springer Netherlands",
number = "4-5",

}

Download

TY - JOUR

T1 - 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

AU - Chevalier, Fabien

AU - Ghulam, Mustafa Malik

AU - Rondet, Damien

AU - Pfannschmidt, Thomas

AU - Merendino, Livia

AU - Lerbs-Mache, Silva

PY - 2015/7

Y1 - 2015/7

N2 - 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.

AB - 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.

KW - Arabidopsis/genetics

KW - Arabidopsis Proteins/genetics

KW - Base Sequence

KW - Binding Sites/genetics

KW - Chloroplasts/genetics

KW - DNA, Intergenic

KW - Endoribonucleases/genetics

KW - Gene Expression

KW - Genes, Plant

KW - Molecular Sequence Data

KW - Mutation

KW - Phosphoproteins/genetics

KW - Photosystem II Protein Complex/genetics

KW - Plants, Genetically Modified

KW - RNA Precursors/genetics

KW - RNA Processing, Post-Transcriptional

KW - RNA, Antisense/genetics

KW - RNA, Plant/genetics

U2 - 10.1007/s11103-015-0325-y

DO - 10.1007/s11103-015-0325-y

M3 - Article

C2 - 26012647

VL - 88

SP - 357

EP - 367

JO - Plant molecular biology

JF - Plant molecular biology

SN - 0167-4412

IS - 4-5

ER -

Von denselben Autoren