TY - JOUR
T1 - Characterization of hypervariable regions in the putative envelope protein of hepatitis C virus
AU - Kato, Nobuyuki
AU - Ootsuyama, Yuko
AU - Ohkoshi, Showgo
AU - Nakazawa, Takahide
AU - Sekiya, Hitomi
AU - Hijikata, Makoto
AU - Shimotohno, Kunitada
N1 - Funding Information:
ACKNOWLEDGMENTS: This study was supported by Grants-in-Aid for Cancer Research and for a Comprehensive lo-Year Strategy for Cancer Control from the Ministry of Health and Welfare of Japan. T.N. and H.S. are recipients of Research Resident Fellowships from the Foundation for Promotion of Cancer Research.
PY - 1992/11/30
Y1 - 1992/11/30
N2 - We previously identified two hypervariable regions [HVR1 (27 amino acids) and HVR2 (7 amino acids)] in the putative envelope glycoprotein (gp70) by comparison of the amino acid sequences of many isolates of the HCV-II genotype. To understand the functional features of these HVRs, using the polymerase chain reaction we analyzed the rate of actual sequence variability in the region including HVR1 and HVR2 of HCV isolated successively at intervals of several months from two patients with chronic C-type hepatitis. In both patients, the amino acid sequence of HVR1, but not HVR2, was found to change dramatically during the observation period (about one amino acid per month). However, no alteration of the amino acid sequence of HVR1 of HCV was observed in a patient in the acute phase of chronic hepatitis. Restriction digestion analysis of sequence diversity showed that a HCV genome with a newly introduced mutation in HVR1 often became the predominant population at the next time of examination. Alterations of amino acids in HVR1 occured sequentially in the two patients in the chronic phase. These findings suggest that mutations in HVR1 are involved in the mechanism of persistent chronic HCV infection.
AB - We previously identified two hypervariable regions [HVR1 (27 amino acids) and HVR2 (7 amino acids)] in the putative envelope glycoprotein (gp70) by comparison of the amino acid sequences of many isolates of the HCV-II genotype. To understand the functional features of these HVRs, using the polymerase chain reaction we analyzed the rate of actual sequence variability in the region including HVR1 and HVR2 of HCV isolated successively at intervals of several months from two patients with chronic C-type hepatitis. In both patients, the amino acid sequence of HVR1, but not HVR2, was found to change dramatically during the observation period (about one amino acid per month). However, no alteration of the amino acid sequence of HVR1 of HCV was observed in a patient in the acute phase of chronic hepatitis. Restriction digestion analysis of sequence diversity showed that a HCV genome with a newly introduced mutation in HVR1 often became the predominant population at the next time of examination. Alterations of amino acids in HVR1 occured sequentially in the two patients in the chronic phase. These findings suggest that mutations in HVR1 are involved in the mechanism of persistent chronic HCV infection.
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U2 - 10.1016/0006-291X(92)91533-V
DO - 10.1016/0006-291X(92)91533-V
M3 - Article
C2 - 1333186
AN - SCOPUS:0027081378
SN - 0006-291X
VL - 189
SP - 119
EP - 127
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -