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. 2000 Mar;74(5):2193–2202. doi: 10.1128/jvi.74.5.2193-2202.2000

FIG. 1.

FIG. 1

Enhancer I mutants derived from 10 patients chronically infected with the hepatitis B virus. (A) DNA binding sites in the HBV enhancer I-X promoter between nt 2364 and 2768 of the HBV genome (pre-C ATG = 1) are depicted. The binding motifs of the liver-specific transcription factors HNF3 and HNF4 are marked in boldface letters. Binding sites for other ubiquitous or liver-specific factors are also shown. (B) Sequence analysis of patient-derived enhancer I regions showing deletions and mutations in comparison to the wt HBV enhancer I region. Between nt 2526 and 2558, the enhancer I sequences are highlighted (boldface italics) to show the mutations found in patients 1 and 3.