J Virol. 1992 September; 66(9): 5313-5319
Genetic variation in vivo and proposed functional domains of the 5' noncoding region of poliovirus RNA.
T Pöyry,
L Kinnunen and
T Hovi
Department of Virology, National Public Health Institute, Helsinki, Finland.
ABSTRACT
Poliovirus has a single-stranded RNA genome of about 7,440 nucleotides (nt) with an unusually long 750-nt noncoding region in the 5' end (5'NCR). Several regulatory functions have been assigned to the 5'NCR. We sequenced the 5'NCRs of 33 wild-type 3 poliovirus strains to study the range and distribution of naturally occurring sequence variations. In this regard, the 5'NCR can be divided into a conserved part (nt 1 to 650) and a hypervariable part (nt 651 to 750). In the conserved part, altogether 234 unevenly distributed nucleotide positions (36%) showed variation. When these positions were plotted against the predicted secondary-structure models, it was found that the existence of most of the proposed stem-loop structures was supported by extensive structure-conserving substitutions in the stems. Regions with conserved sequences, as well as mutational hot spots, were observed. The hypervariable part of the 5'NCR varied up to 56% between the strains studied. The A + U percentage was significantly higher than in the conserved part. The number of AUG codons varied between 5 and 15 in the conserved part of the 5'NCR, while none was found in the hypervariable part. These results provide information that can be used in site-directed mutagenesis and other approaches targeted to reveal the functional domains of the 5'NCR.
J Virol. 1992 September; 66(9): 5313-5319
This article has been cited by other articles:
-
Costafreda, M. I., Bosch, A., Pinto, R. M.
(2006). Development, Evaluation, and Standardization of a Real-Time TaqMan Reverse Transcription-PCR Assay for Quantification of Hepatitis A Virus in Clinical and Shellfish Samples.. Appl. Environ. Microbiol.
72: 3846-3855
[Abstract]
[Full Text]
-
DeJesus, N., Franco, D., Paul, A., Wimmer, E., Cello, J.
(2005). Mutation of a Single Conserved Nucleotide between the Cloverleaf and Internal Ribosome Entry Site Attenuates Poliovirus Neurovirulence. J. Virol.
79: 14235-14243
[Abstract]
[Full Text]
-
Liu, H.-M., Zheng, D.-P., Zhang, L.-B., Oberste, M. S., Kew, O. M., Pallansch, M. A.
(2003). Serial Recombination during Circulation of Type 1 Wild-Vaccine Recombinant Polioviruses in China. J. Virol.
77: 10994-11005
[Abstract]
[Full Text]
-
Dahourou, G., Guillot, S., Le Gall, O., Crainic, R.
(2002). Genetic recombination in wild-type poliovirus. J. Gen. Virol.
83: 3103-3110
[Abstract]
[Full Text]
-
Venkatesan, A., Dasgupta, A.
(2001). Novel Fluorescence-Based Screen To Identify Small Synthetic Internal Ribosome Entry Site Elements. Mol. Cell. Biol.
21: 2826-2837
[Abstract]
[Full Text]
-
Nateri, A. S., Hughes, P. J., Stanway, G.
(2000). In Vivo and In Vitro Identification of Structural and Sequence Elements of the Human Parechovirus 5' Untranslated Region Required for Internal Initiation. J. Virol.
74: 6269-6277
[Abstract]
[Full Text]
-
Gan, W., Celle, M. L., Rhoads, R. E.
(1998). Functional Characterization of the Internal Ribosome Entry Site of eIF4G mRNA. J. Biol. Chem.
273: 5006-5012
[Abstract]
[Full Text]
-
Muir, P., Kammerer, U., Korn, K., Mulders, M. N., Poyry, T., Weissbrich, B., Kandolf, R., Cleator, G. M., van Loon, A. M.
(1998). Molecular Typing of Enteroviruses: Current Status and Future Requirements. Clin. Microbiol. Rev.
11: 202-227
[Abstract]
[Full Text]
Copyright © 1992 by the American Society for Microbiology. All rights reserved.