Division of Virology, Paul-Ehrlich-Institut, D-63225 Langen, Germany.
Department of Gastroenterology and Hepatology, J. W. Goethe University, D-60590 Frankfurt, Germany.
Cells. 2020 Aug 13;9(8):1898. doi: 10.3390/cells9081898.
The N-terminus of the hepatitis B virus (HBV) large surface protein (LHB) differs with respect to genotypes. Compared to the amino terminus of genotype (Gt)D, in GtA, GtB and GtC, an additional identical 11 amino acids (aa) are found, while GtE and GtG share another similar 10 aa. Variants of GtB and GtC affecting this N-terminal part are associated with hepatoma formation. Deletion of these amino-terminal 11 aa in GtA reduces the amount of LHBs and changes subcellular accumulation (GtA-like pattern) to a dispersed distribution (GtD-like pattern). Vice versa, the fusion of the GtA-derived N-terminal 11 aa to GtD causes a GtA-like phenotype. However, insertion of the corresponding GtE-derived 10 aa to GtD has no effect. Deletion of these 11aa decreases filament size while neither the number of released viral genomes nor virion size and infectivity are affected. A negative regulatory element (aa 2-8) and a dominant positive regulatory element (aa 9-11) affecting the amount of LHBs were identified. The fusion of this motif to eGFP revealed that the effect on protein amount and subcellular distribution is not restricted to LHBs. These data identify a novel region in the N-terminus of LHBs affecting the amount and subcellular distribution of LHBs and identify release-promoting and -inhibiting aa residues within this motive.
乙型肝炎病毒(HBV)大表面蛋白(LHB)的 N 端在基因型方面存在差异。与基因型(Gt)D 的氨基端相比,在 GtA、GtB 和 GtC 中发现了另外相同的 11 个氨基酸(aa),而 GtE 和 GtG 则具有另一个相似的 10 个 aa。影响这个 N 端的 GtB 和 GtC 变体与肝癌形成有关。在 GtA 中删除这些氨基末端的 11 个 aa 会减少 LHBs 的数量并改变亚细胞积累(GtA 样模式)为分散分布(GtD 样模式)。反之,将源自 GtA 的 N 端的 11 个 aa 融合到 GtD 上会导致 GtA 样表型。然而,将相应的源自 GtE 的 10 个 aa 插入到 GtD 中没有影响。删除这些 11 个 aa 会减小纤维丝的大小,而释放的病毒基因组的数量以及病毒体的大小和感染力不受影响。鉴定了影响 LHBs 数量的负调控元件(aa 2-8)和显性正调控元件(aa 9-11)。将该基序融合到 eGFP 上表明,对蛋白数量和亚细胞分布的影响不仅限于 LHBs。这些数据确定了 LHBs 的 N 端的一个新区域,该区域影响 LHBs 的数量和亚细胞分布,并确定了该基序内促进和抑制释放的 aa 残基。