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1 Laboratory of Infectious Diseases, Building 7, Room 100, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892
and2 Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, U.S.A.
The sequences of the human parainfluenza virus type 3 (PIV3) matrix (M) mRNA [1150 nucleotides exclusive of poly(A)] and predicted M protein (353 amino acids) were determined by sequence analysis of cloned cDNA and viral genomic RNA. The geneend sequence of the M gene differed from the semi-conserved gene-end sequence of the other PIV3 genes by an apparent insertion of eight nucleotides. The PIV3 M protein shared high sequence homology with Sendai virus and moderate homology with measles virus and canine distemper virus. Statistical analysis of the available sequences showed that the M protein was the most highly conserved parainfluenza viral protein.
Keywords: sequence analysis, matrix protein, paramyxovirus evolution
Received 12 January 1987;
accepted 10 February 1987.
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