TY - JOUR
T1 - Comparison of the three large polymerase proteins of influenza A, B, and C viruses
AU - Yamashita, Makoto
AU - Krystal, Mark
AU - Palese, Peter
N1 - Funding Information:
We thank Dr. S. Minato, director of Bioscience Research Laboratories, Sankyo Co. Ltd., for supporting the sabbatical leave of M.Y. at the Mount Sinar School of Medicine. This workwas also supported by Merit Award Al-l 8998 (P.P.) and by Public Health Service Grants Al-2663 (M.K.) and Al-24460, and Al-l 1823 (P.P.) from the National Institutes of Health. M.K. also is supported by funds from the New York Lung Association and an Irma T. Hirsch1 Scholar Award.
PY - 1989/8
Y1 - 1989/8
N2 - The three large RNA segments of influenza C virus C/JJ/50 were cloned and sequenced, and the deduced amino acid sequences were compared with those of the polymerase (P) proteins of influenza A and B viruses. The coding strategy of the C virus RNA segments is the same as that for the large A and B virus segments as one long open reading frame is present in each segment. RNA segment 1 of influenza C virus encodes the equivalent of the PB2 protein; it has an approximate 25% sequence identity with the corresponding (cap binding) influenza A and B virus PB2 proteins. The PB1 protein of influenza C virus, coded for by segment 2, has an approximate 40% sequence identity with the corresponding proteins of influenza A and B viruses including the Asp-Asp sequence motif found in many RNA polymerase molecules. The PB1 polymerase is thus the most highly conserved protein among the influenza A, B, and C viruses. Although the protein coded for by RNA 3 of influenza C virus shows an approximate 25% sequence identity with the acid polymerase (PA) proteins of the A and B viruses, its sequence does not display any acid charge features at neutral pH. This protein is thus referred to as the P3 (rather than the PA) protein of influenza C virus.
AB - The three large RNA segments of influenza C virus C/JJ/50 were cloned and sequenced, and the deduced amino acid sequences were compared with those of the polymerase (P) proteins of influenza A and B viruses. The coding strategy of the C virus RNA segments is the same as that for the large A and B virus segments as one long open reading frame is present in each segment. RNA segment 1 of influenza C virus encodes the equivalent of the PB2 protein; it has an approximate 25% sequence identity with the corresponding (cap binding) influenza A and B virus PB2 proteins. The PB1 protein of influenza C virus, coded for by segment 2, has an approximate 40% sequence identity with the corresponding proteins of influenza A and B viruses including the Asp-Asp sequence motif found in many RNA polymerase molecules. The PB1 polymerase is thus the most highly conserved protein among the influenza A, B, and C viruses. Although the protein coded for by RNA 3 of influenza C virus shows an approximate 25% sequence identity with the acid polymerase (PA) proteins of the A and B viruses, its sequence does not display any acid charge features at neutral pH. This protein is thus referred to as the P3 (rather than the PA) protein of influenza C virus.
UR - http://www.scopus.com/inward/record.url?scp=0024411767&partnerID=8YFLogxK
U2 - 10.1016/0042-6822(89)90615-6
DO - 10.1016/0042-6822(89)90615-6
M3 - Article
C2 - 2763462
AN - SCOPUS:0024411767
SN - 0042-6822
VL - 171
SP - 458
EP - 466
JO - Virology
JF - Virology
IS - 2
ER -