Tong S P, Li J S, Vitvitski L, Kay A, Treépo C
Unité de Recherche sur les Hepatites, le SIDA et les Rétrovirus Humains, Institut National de la Sant' et de la Recherche Médicale 271, Lyon, France.
J Virol. 1993 Sep;67(9):5651-5. doi: 10.1128/JVI.67.9.5651-5655.1993.
In two natural HBe-minus hepatitis B virus mutants, expression of HBe protein was abrogated by a nonsense mutation at precore codon 28 and a frameshift mutation at codon 29, respectively. Both mutants contained an additional nucleotide substitution(s) which was found by transfection experiments to be required for efficient packaging of pregenomic RNA. The observed mutational profiles were consistent with the presence of a base-paired region of the pregenome encapsidation signal overlapping the HBe-coding sequence. Results obtained with artificial mutants with significant changes in the primary sequence suggested that base pairing is required but insufficient for efficient pregenome packaging. However, the predicted first four base pairs of the stem are dispensable.
在两个自然缺失HBe的乙型肝炎病毒突变体中,前核心密码子28处的无义突变和密码子29处的移码突变分别消除了HBe蛋白的表达。两个突变体都含有一个额外的核苷酸替换,通过转染实验发现这是有效包装前基因组RNA所必需的。观察到的突变谱与前基因组包装信号的碱基配对区域与HBe编码序列重叠的情况一致。对一级序列有显著变化的人工突变体的研究结果表明,碱基配对是有效包装前基因组所必需的,但并不充分。然而,茎的预测前四个碱基对是可有可无的。