An atypical 3′-controller element mediates low-level transcription of the p6 subgenomic mRNA ofCitrus tristeza virus
- 1 March 2005
- journal article
- Published by Wiley in Molecular Plant Pathology
- Vol. 6 (2) , 165-176
- https://doi.org/10.1111/j.1364-3703.2005.00275.x
Abstract
SUMMARY Citrus tristeza virus (CTV) has within the 3'-half of the genome ten open reading frames (ORFs) that are expressed through a series of 3'-coterminal subgenomic (sg) messenger (m)RNAs that, in general, function as monocistronic mRNAs with only the 5'-most ORF translated. Yet only nine sg mRNAs have been detected, suggesting that ORF 3, which is predicted to encode a small hydrophobic protein of approximately 6 kDa (p6), might be expressed in some other manner, perhaps from a functionally dicistronic sg mRNA. However, when we positioned the p6 gene near the 3'-terminus of a minimal CTV replicon to amplify greatly the level of production of the putative sg mRNA, we found a minimal level of a p6 mRNA, thus providing evidence for a separate mRNA for each 3' ORF. The 5' termini of the sg mRNAs and the cis-acting elements (controller elements-CEs) that regulate the production of the p6 gene and the adjacent HSP70h (heat shock protein 70 homologue) were located further upstream of the ORFs compared with the other CTV CEs. Both preferentially initiated synthesis with an adenylate, as has been shown for the more highly expressed 3' genes; but in contrast, the p6 sg mRNA occasionally initiated with a guanylate. Although the nucleotide sequences and the computer-predicted secondary structures of the HSP70h CE were similar to those previously described for other 3' CEs, those of the p6 CE were quite different, suggesting that CE strength is related to proximity to an ideal CE conformation. The lack of similarity between different CTV CEs led us to examine how well the CTV replicase complex could initiate sg mRNAs from CEs from different members of the family Closteroviridae. We found that the CTV replicase complex efficiently initiated production of sgRNAs from the p6 and HSP70h CEs from Beet yellows virus, with the HSP70h CE initiating at the same nucleotide as within the homologous virus, indicating that the mode of recognition of the CEs is similar. However, CEs from a more distantly related member of the Closteroviridae, Lettuce infectious yellows virus, did not function to produce sg mRNAs in CTV.Keywords
This publication has 27 references indexed in Scilit:
- cis-acting elements at opposite ends of the Citrus tristeza virus genome differ in initiation and termination of subgenomic RNAsVirology, 2004
- Effects of Modification of the Transcription Initiation Site Context on Citrus Tristeza Virus Subgenomic RNA SynthesisJournal of Virology, 2003
- Transcription Strategy in a Closterovirus: a Novel 5′-Proximal Controller Element of Citrus Tristeza Virus Produces 5′- and 3′-Terminal Subgenomic RNAs and Differs from 3′ Open Reading Frame Controller ElementsJournal of Virology, 2003
- Characterization of the cis-Acting Elements Controlling Subgenomic mRNAs of Citrus tristeza virus: Production of Positive- and Negative-Stranded 3′-Terminal and Positive-Stranded 5′-Terminal RNAsVirology, 2001
- Sequences of Citrus Tristeza Virus Separated in Time and Space Are Essentially IdenticalJournal of Virology, 2000
- Genetic Analysis of the Cell-to-Cell Movement of Beet Yellows ClosterovirusVirology, 2000
- The complete genome sequence of the major component of a mild citrus tristeza virus isolate.Journal of General Virology, 1999
- Algorithms and Thermodynamics for RNA Secondary Structure Prediction: A Practical GuidePublished by Springer Nature ,1999
- A New Model for Coronavirus TranscriptionPublished by Springer Nature ,1998
- Characterization of Citrus Tristeza Virus Subgenomic RNAs in Infected TissueVirology, 1995