病毒学
聚合酶
逆转录酶
生物
乙型肝炎病毒
乙型肝炎表面抗原
拉米夫定
病毒
分子生物学
遗传学
基因
聚合酶链反应
作者
Lieven Stuyver,Stephen Locarnini,Anna S. Lok,Douglas D. Richman,William F. Carman,Jules L. Dienstag,Raymond F. Schinazi
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2001-03-01
卷期号:33 (3): 751-757
被引量:390
标识
DOI:10.1053/jhep.2001.22166
摘要
There is currently no universally accepted numbering convention for the antiviral drug-related resistance mutations in the reverse transcriptase (rt) domain of the human hepatitis B virus (HBV) polymerase. The published inconsistencies have resulted from different HBV genotypes. A standardized numbering system for HBV polymerase is proposed. The new system is based on functional observations of HBV surface gene proteins (preS1, preS2, and HBsAg) and on the current convention used for human immunodeficiency virus type 1 (HIV-1) polymerase proteins (protease, rt, and integrase), in which the amino acid numbering restarts at the first codon position of each domain. The HBV polymerase protein can be divided into 4 domains (terminal protein, spacer, rt, ribonuclease H) and each of these can be numbered separately. In this proposal, the HBV rt domain starts with the highly conserved EDWGPCDEHG motif, contains 344 amino acids, and the lamivudine-related resistance mutations are found at amino acid rtL180M (previously amino acid 528, 526, 515, or 525) and rtM204V/I (previously 552, 550, 539, or 549). The new consensus rt domain numbering system is genotype independent and allows investigators to number any previously and newly discovered antiviral-related amino acid change in a standardized manner.
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