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pubmed-article:8376962pubmed:abstractTextNone of the mutations so far discovered in several hepatitis delta virus (HDV) isolates appears to determine important changes in HDV specific protein (HDAg) expression, except for a putative mutation at nucleotide 1012 converting an amber stop codon (TAG) to a codon for tryptophan (TGG). Here we present the characterization of an HDV obtained from the liver of a woodchuck inoculated with sera from fulminant HDV patients in Central African Republic (CAR). By restriction enzyme analysis and sequencing of HDAg-coding region cDNA clones, we found that this HDV isolate bears a novel mutation (T to A) at nucleotide 1013 which converts the amber stop codon (TAG) to a codon for lysine (AAG). Comparison of these nucleotide sequences with those available from American, Japanese, Taiwanese, French, Italian and Nauru isolates showed a variability of 1.7 to 21.5% and 1.9 to 28.7% at the nucleic acid and amino acid levels, respectively. The HDAg-encoding sequence of the CAR isolate is closely related to that of the Italian HDV isolate. The in vitro expression of this HDV isolate resulted in a unique HDAg species (28K) which was identical with that characterized in vivo.lld:pubmed
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pubmed-article:8376962pubmed:volume74 ( Pt 9)lld:pubmed
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pubmed-article:8376962pubmed:pagination1827-35lld:pubmed
pubmed-article:8376962pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8376962pubmed:articleTitleDiscovery of a novel point mutation changing the HDAg expression of a hepatitis delta virus isolate from Central African Republic.lld:pubmed
pubmed-article:8376962pubmed:affiliationInstitut National de la Santé et de la Recherche Médicale (INSERM) U 271, Lyon, France.lld:pubmed
pubmed-article:8376962pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8376962pubmed:publicationTypeComparative Studylld:pubmed
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