Processing of nuclear viroids in vivo: an interplay between RNA conformations.

Replication of viroids, small non-protein-coding plant pathogenic RNAs, entails reiterative transcription of their incoming single-stranded circular genomes, to which the (+) polarity is arbitrarily assigned, cleavage of the oligomeric strands of one or both polarities to unit-length, and ligation t...

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Main Authors: María-Eugenia Gas, Carmen Hernández, Ricardo Flores, José-Antonio Daròs
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-11-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC2098832?pdf=render
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author María-Eugenia Gas
Carmen Hernández
Ricardo Flores
José-Antonio Daròs
author_facet María-Eugenia Gas
Carmen Hernández
Ricardo Flores
José-Antonio Daròs
author_sort María-Eugenia Gas
collection DOAJ
description Replication of viroids, small non-protein-coding plant pathogenic RNAs, entails reiterative transcription of their incoming single-stranded circular genomes, to which the (+) polarity is arbitrarily assigned, cleavage of the oligomeric strands of one or both polarities to unit-length, and ligation to circular RNAs. While cleavage in chloroplastic viroids (family Avsunviroidae) is mediated by hammerhead ribozymes, where and how cleavage of oligomeric (+) RNAs of nuclear viroids (family Pospiviroidae) occurs in vivo remains controversial. Previous in vitro data indicated that a hairpin capped by a GAAA tetraloop is the RNA motif directing cleavage and a loop E motif ligation. Here we have re-examined this question in vivo, taking advantage of earlier findings showing that dimeric viroid (+) RNAs of the family Pospiviroidae transgenically expressed in Arabidopsis thaliana are processed correctly. Using this methodology, we have mapped the processing site of three members of this family at equivalent positions of the hairpin I/double-stranded structure that the upper strand and flanking nucleotides of the central conserved region (CCR) can form. More specifically, from the effects of 16 mutations on Citrus exocortis viroid expressed transgenically in A. thaliana, we conclude that the substrate for in vivo cleavage is the conserved double-stranded structure, with hairpin I potentially facilitating the adoption of this structure, whereas ligation is determined by loop E and flanking nucleotides of the two CCR strands. These results have deep implications on the underlying mechanism of both processing reactions, which are most likely catalyzed by enzymes different from those generally assumed: cleavage by a member of the RNase III family, and ligation by an RNA ligase distinct from the only one characterized so far in plants, thus predicting the existence of at least a second plant RNA ligase.
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spelling doaj.art-0236623db6fb4a5093381174dd98f7212022-12-22T01:01:19ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742007-11-01311e18210.1371/journal.ppat.0030182Processing of nuclear viroids in vivo: an interplay between RNA conformations.María-Eugenia GasCarmen HernándezRicardo FloresJosé-Antonio DaròsReplication of viroids, small non-protein-coding plant pathogenic RNAs, entails reiterative transcription of their incoming single-stranded circular genomes, to which the (+) polarity is arbitrarily assigned, cleavage of the oligomeric strands of one or both polarities to unit-length, and ligation to circular RNAs. While cleavage in chloroplastic viroids (family Avsunviroidae) is mediated by hammerhead ribozymes, where and how cleavage of oligomeric (+) RNAs of nuclear viroids (family Pospiviroidae) occurs in vivo remains controversial. Previous in vitro data indicated that a hairpin capped by a GAAA tetraloop is the RNA motif directing cleavage and a loop E motif ligation. Here we have re-examined this question in vivo, taking advantage of earlier findings showing that dimeric viroid (+) RNAs of the family Pospiviroidae transgenically expressed in Arabidopsis thaliana are processed correctly. Using this methodology, we have mapped the processing site of three members of this family at equivalent positions of the hairpin I/double-stranded structure that the upper strand and flanking nucleotides of the central conserved region (CCR) can form. More specifically, from the effects of 16 mutations on Citrus exocortis viroid expressed transgenically in A. thaliana, we conclude that the substrate for in vivo cleavage is the conserved double-stranded structure, with hairpin I potentially facilitating the adoption of this structure, whereas ligation is determined by loop E and flanking nucleotides of the two CCR strands. These results have deep implications on the underlying mechanism of both processing reactions, which are most likely catalyzed by enzymes different from those generally assumed: cleavage by a member of the RNase III family, and ligation by an RNA ligase distinct from the only one characterized so far in plants, thus predicting the existence of at least a second plant RNA ligase.http://europepmc.org/articles/PMC2098832?pdf=render
spellingShingle María-Eugenia Gas
Carmen Hernández
Ricardo Flores
José-Antonio Daròs
Processing of nuclear viroids in vivo: an interplay between RNA conformations.
PLoS Pathogens
title Processing of nuclear viroids in vivo: an interplay between RNA conformations.
title_full Processing of nuclear viroids in vivo: an interplay between RNA conformations.
title_fullStr Processing of nuclear viroids in vivo: an interplay between RNA conformations.
title_full_unstemmed Processing of nuclear viroids in vivo: an interplay between RNA conformations.
title_short Processing of nuclear viroids in vivo: an interplay between RNA conformations.
title_sort processing of nuclear viroids in vivo an interplay between rna conformations
url http://europepmc.org/articles/PMC2098832?pdf=render
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AT ricardoflores processingofnuclearviroidsinvivoaninterplaybetweenrnaconformations
AT joseantoniodaros processingofnuclearviroidsinvivoaninterplaybetweenrnaconformations