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Journal of Virology, September 2000, p. 8558-8562, Vol. 74, No. 18
Departamento de Patología Experimental, Centro de
Investigación y de Estudios Avanzados del IPN, Mexico City,
Mexico,1 and Center for Pediatric
Research, Children's Hospital for the King's Daughters, Eastern
Virginia Medical School, Norfolk, Virginia2
Received 29 February 2000/Accepted 20 June 2000
The lack of a susceptible cell line and an animal model for Norwalk
virus (NV) infection has prompted the development of alternative strategies to generate in vitro RNAs that approximate the authentic viral genome. This approach has allowed the study of viral RNA replication and gene expression. In this study, using mobility shift
and cross-linking assays, we detected several cellular proteins from
HeLa and CaCo-2 cell extracts that bind to, and form stable complexes
with, the first 110 nucleotides of the 5' end of NV genomic RNA, a
region previously predicted to form a double stem-loop structure. These
proteins had molecular weights similar to those of the HeLa cellular
proteins that bind to the internal ribosomal entry site of poliovirus
RNA. HeLa proteins La, PCBP-2, and PTB, which are important for
poliovirus translation, and hnRNP L, which is possibly implicated in
hepatitis C virus translation, interact with NV RNA. These protein-RNA
interactions are likely to play a role in NV translation and/or replication.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Interaction of Cellular Proteins with the 5' End
of Norwalk Virus Genomic RNA
*
Corresponding author. Mailing address: Departamento de
Patología Experimental, Centro de Investigación y de
Estudios Avanzados del IPN, Av. IPN 2508, Col. San Pedro Zacatenco,
México, D.F. C.P. 07360, México. Phone: (52)5
747-3800, ext. 5647. Fax: (52)5 747-7107. E-mail:
alonso{at}mail.cinvestav.mx.
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