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자료유형
학술저널
저자정보
저널정보
거트앤리버 발행위원회 Gut and Liver Gut and Liver 제7권 제5호
발행연도
2013.1
수록면
569 - 575 (7page)

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Background/Aims: The hepatitis B virus (HBV) genome contains binding sites for hepatocyte nuclear factors (HNF) 3and 4 in the core domain of enhancer 1 (Enh1), and mutations in this domain have a strong impact on virus replication. We aimed to identify frequent base-mutation sites in the core domain of Enh1 and to examine the impact of these mutations on viral replication. Methods: We studied virological characteristics and genetic sequences in 387 patients with chronic hepatitis B. We evaluated functional differences associated with specific mutations within the core domain of Enh1. Results: Mutations in the core domain were found with significant frequency in C1126 (122/387 [31.5%], the binding site for HNF3) and in C1134 (106/387 [27.4%], the binding site for HNF4). A single mutation at nt 1126 (C1126)was identified in 17/123 (13.8%), and 105/123 (85.4%)had double mutations (C1126/1134). The level of HBV DNA (log10 copies/mL) was lower in single mutants (C1126,5.81±1.25) than in wild (6.80±1.65) and double mutants (C1126/1134, 6.81±1.54). Similarly, the relative luciferase activity of C1126 and C1126/C1134 was 0.18 and 1.12times that of the wild-type virus, respectively. Conclusions:Mutations in the HNF3 binding site inhibit viral replication,whereas mutations at the HNF4 binding site restore viral replication.

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