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Journal of Virology, October 2000, p. 9167-9174, Vol. 74, No. 19
Division of Basic Sciences, Fred Hutchinson
Cancer Research Center, Seattle, Washington 98109
Received 10 December 1999/Accepted 11 July 2000
We previously showed that the yeast three-hybrid system provides a
genetic assay of both RNA and protein components for avian retroviral
RNA encapsidation. In the current study, we used this assay to
precisely define cis-acting determinants involved in avian
leukosis sarcoma virus packaging RNA binding to Gag protein. In vivo
screening of Rous sarcoma virus mutants was performed with randomly
mutated minimal packaging sequences (M
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Yeast Three-Hybrid Screening of Rous Sarcoma Virus
Mutants with Randomly Mutagenized Minimal Packaging Signals Reveals
Regions Important for Gag Interactions
) made using PCR amplification
after cotransformation with Gag
PR protein into yeast cells. Colonies
with low
-galactosidase activity were analyzed to locate mutations
in M
sequences affecting binding to Gag proteins. This genetic assay
delineated secondary structural elements that are important for
efficient RNA binding, including a single-stranded small bulge
containing the initiation codon for uORF3, as well as adjacent stem
structures. This implies a possible tertiary structure favoring the
high-affinity binding sites for Gag. In most cases, results from the
three-hybrid assay were well correlated with those from the viral RNA
packaging assays. The results from random mutagenesis using the rapid
three-hybrid binding assay are consistent with those from site-directed
mutagenesis using in vivo packaging assays.
*
Corresponding author. Mailing address: Division of
Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview
Ave. N., Seattle, WA 98109-1024. Phone: (206) 667-4442. Fax: (206) 667-5939. E-mail: mlinial{at}fhcrc.org.
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