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PMID: 8113760 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

An estimation of the nucleotide substitution rate at defined positions in the influenza virus haemagglutinin gene.

The Journal of general virology ·Vol. 75 ( Pt 2) ·1994-02-00 ·Pages 389-93

Suárez-López P, Ortín J

Abstract

The mutation rates to a viable mar (monoclonal antibody-resistant mutant) genotype of wild-type influenza (A/Victoria/3/75; H3N2) virus or its mutator variant strains have been previously determined. In order to estimate the mutation rates per nucleotide position, the sequence alterations present in 44 mar mutants isolated from either the wild-type or the mut43 mutator strain have been determined. These mar mutants were selected with either of two non-overlapping, haemagglutinin-specific, monoclonal antibodies (2G10 and p7). Most of the protein changes were identified as substitutions of large, charged amino acids for glycine residues, as the result of G to A transitions. Particularly interesting amino acid changes, not previously reported, were observed in the p7 monoclonal antibody-specific mutants, in which only Gly to Ser and Gly to Asp at position 226 were detected. The identification of the nucleotide substitutions responsible for the mar phenotype has allowed the calculation of approximate values for the total mutation rates at these positions.

MeSH Terms
Amino Acid Sequence Antibodies, Monoclonal/immunology Base Sequence Hemagglutinin Glycoproteins, Influenza Virus Hemagglutinins, Viral/genetics Influenza A virus/genetics Molecular Sequence Data Mutation
Chemicals
Antibodies, Monoclonal Hemagglutinin Glycoproteins, Influenza Virus Hemagglutinins, Viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Suárez-López P
Centro Nacional de Biotecnología (CSIC), Universidad Autónoma de Madrid, Spain.
Ortín J
Article Info
Journal
The Journal of general virology
Abbr.
J Gen Virol
ISSN
0022-1317
Published
1994-02-00
Pages
389-93
Language
English
Region
England
NLM ID
0077340
Subset
IM
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