Literature DB >> 7214524

Near identity of 3- RNA secondary structure in bromoviruses and cucumber mosaic virus.

P Ahlquist, R Dasgupta, P Kaesberg.   

Abstract

The 3- terminal sequences of RNAs 1, 2, 3 and 4 from each of the three bromoviruses (brome mosaic, cowpea chlorotic mottle and broad bean mottle viruses) and also from cucumber mosaic virus display interviral sequence similarity in addition to strong intraviral homology. Interviral similarity is much more evident when RNA secondary, rather than primary, structures are compared. The last 190 bases of the various RNAs can fold into strikingly similar, extensively base-paired secondary structures whose common features are supported by RNA structure mapping. The extreme 3' end of each viral RNA can base-pair in two distinct configurations. Bromovirus RNA 3s each contain an unusually accessible internal oligo(A) sequence which, in brome mosaic virus at least, is located in the intercistronic noncoding region. Functional implications of these structural features are discussed.

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Year:  1981        PMID: 7214524     DOI: 10.1016/0092-8674(81)90283-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  65 in total

1.  Genetic recombination in brome mosaic virus: effect of sequence and replication of RNA on accumulation of recombinants.

Authors:  P D Nagy; J J Bujarski
Journal:  J Virol       Date:  1992-11       Impact factor: 5.103

2.  Generation and analysis of nonhomologous RNA-RNA recombinants in brome mosaic virus: sequence complementarities at crossover sites.

Authors:  J J Bujarski; A M Dzianott
Journal:  J Virol       Date:  1991-08       Impact factor: 5.103

3.  Localization of the replicase recognition site within brome mosaic virus RNA by hybrid-arrested RNA synthesis.

Authors:  P Ahlquist; J J Bujarski; P Kaesberg; T C Hall
Journal:  Plant Mol Biol       Date:  1984-01       Impact factor: 4.076

4.  Contributions of the brome mosaic virus RNA-3 3'-nontranslated region to replication and translation.

Authors:  F C Lahser; L E Marsh; T C Hall
Journal:  J Virol       Date:  1993-06       Impact factor: 5.103

5.  The turnip yellow mosaic virus tRNA-like structure cannot be replaced by generic tRNA-like elements or by heterologous 3' untranslated regions known to enhance mRNA expression and stability.

Authors:  J M Skuzeski; C S Bozarth; T W Dreher
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

6.  Resected RNA pseudoknots and their recognition by histidyl-tRNA synthetase.

Authors:  B Felden; R Giegé
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

7.  Infectious RNA derived by transcription from cloned cDNA copies of the genomic RNA of an insect virus.

Authors:  B Dasmahapatra; R Dasgupta; K Saunders; B Selling; T Gallagher; P Kaesberg
Journal:  Proc Natl Acad Sci U S A       Date:  1986-01       Impact factor: 11.205

8.  CUUCGG hairpins: extraordinarily stable RNA secondary structures associated with various biochemical processes.

Authors:  C Tuerk; P Gauss; C Thermes; D R Groebe; M Gayle; N Guild; G Stormo; Y d'Aubenton-Carafa; O C Uhlenbeck; I Tinoco
Journal:  Proc Natl Acad Sci U S A       Date:  1988-03       Impact factor: 11.205

9.  Nucleotide sequence of the 3'-terminal tRNA-like structure in barley stripe mosaic virus genome.

Authors:  V V Rupasov; D M Adyshev; S N Belgelarskaya; A A Agranovsky; A S Mankin; V V Dolja; J G Atabekov
Journal:  Nucleic Acids Res       Date:  1984-05-11       Impact factor: 16.971

10.  Characterization and engineering of sequences controlling in vivo synthesis of brome mosaic virus subgenomic RNA.

Authors:  R French; P Ahlquist
Journal:  J Virol       Date:  1988-07       Impact factor: 5.103

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