Literature DB >> 11448167

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 RNAs.

S Gowda1, T Satyanarayana, M A Ayllón, M R Albiach-Martí, M Mawassi, S Rabindran, S M Garnsey, W O Dawson.   

Abstract

Citrus tristeza virus (CTV), a member of the Closteroviridae, has an approximately 20-kb positive-sense RNA genome with two 5' ORFs translated from the genomic RNA and 10 3' genes expressed via nine or ten 3'-terminal subgenomic (sg) RNAs. The expression of the 3' genes appears to have properties intermediate between the smaller viruses of the "alphavirus supergroup" and the larger viruses of the Coronaviridae. The sgRNAs are contiguous with the genome, without a common 5' leader, and are associated with large amounts of complementary sgRNAs. Production of the different sgRNAs is regulated temporally and quantitatively, with the highly expressed genes having noncoding regions (NCR) 5' of the ORFs. The cis-acting elements that control the highly expressed major coat protein (CP) gene and the intermediately expressed minor coat protein (CPm) gene were mapped and compared. Mutational analysis showed that the CP sgRNA controller element mapped within nts -47 to -5 upstream of the transcription start site, entirely within the NCR, while the CPm control region mapped within a 57 nt sequence within the upstream ORF. Although both regions were predicted to fold into two stem-loop structures, mutagenesis suggested that primary structure might be more important than the secondary structure. Because each controller element produced large amounts of 3'-terminal positive- and negative-stranded sgRNAs, we could not differentiate whether the cis-acting element functioned as a promoter or terminator, or both. Reversal of the control element unexpectedly produced large amounts of a negative-stranded sgRNA apparently by termination of negative-stranded genomic RNA synthesis. Further examination of controller elements in their native orientation showed normal production of abundant amounts of positive-stranded sgRNAs extending to near the 5'-terminus, corresponding to termination at each controller element. Thus, each controller element produced three sgRNAs, a 5'-terminal positive strand and both positive- and negative-stranded 3'-terminal RNAs. Therefore, theoretically CTV could produce 30-33 species of RNAs in infected cells. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11448167     DOI: 10.1006/viro.2001.0987

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  26 in total

1.  A complex network of RNA-RNA interactions controls subgenomic mRNA transcription in a tombusvirus.

Authors:  Han-Xin Lin; K Andrew White
Journal:  EMBO J       Date:  2004-07-29       Impact factor: 11.598

2.  A multicomponent RNA-based control system regulates subgenomic mRNA transcription in a tombusvirus.

Authors:  Han-Xin Lin; Wei Xu; K Andrew White
Journal:  J Virol       Date:  2006-12-13       Impact factor: 5.103

3.  Uncoupling RNA virus replication from transcription via the polymerase: functional and evolutionary insights.

Authors:  Baodong Wu; K Andrew White
Journal:  EMBO J       Date:  2007-11-22       Impact factor: 11.598

4.  The p23 protein of citrus tristeza virus controls asymmetrical RNA accumulation.

Authors:  Tatineni Satyanarayana; Siddarame Gowda; María A Ayllón; María R Albiach-Martí; Shailaja Rabindran; William O Dawson
Journal:  J Virol       Date:  2002-01       Impact factor: 5.103

5.  Shrink the giant: scale down the citrus tree to a model system to investigate the RNA interference efficiency.

Authors:  Nabil Killiny
Journal:  Plant Signal Behav       Date:  2019-05-01

6.  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 elements.

Authors:  Siddarame Gowda; María A Ayllón; Tatineni Satyanarayana; Moshe Bar-Joseph; William O Dawson
Journal:  J Virol       Date:  2003-01       Impact factor: 5.103

7.  Glycosylation of gp41 of simian immunodeficiency virus shields epitopes that can be targets for neutralizing antibodies.

Authors:  Eloìsa Yuste; Jacqueline Bixby; Jeffrey Lifson; Shuji Sato; Welkin Johnson; Ronald Desrosiers
Journal:  J Virol       Date:  2008-10-01       Impact factor: 5.103

8.  Effects of modification of the transcription initiation site context on citrus tristeza virus subgenomic RNA synthesis.

Authors:  María A Ayllón; Siddarame Gowda; Tatineni Satyanarayana; Alexander V Karasev; Scott Adkins; Munir Mawassi; José Guerri; Pedro Moreno; William O Dawson
Journal:  J Virol       Date:  2003-09       Impact factor: 5.103

9.  The 64-kilodalton capsid protein homolog of Beet yellows virus is required for assembly of virion tails.

Authors:  Alberto J Napuli; Dina V Alzhanova; Catalin E Doneanu; Douglas F Barofsky; Eugene V Koonin; Valerian V Dolja
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

10.  Closterovirus bipolar virion: evidence for initiation of assembly by minor coat protein and its restriction to the genomic RNA 5' region.

Authors:  Tatineni Satyanarayana; Siddarame Gowda; María A Ayllón; William O Dawson
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-12       Impact factor: 11.205

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