Roles of the three major phosphorylation sites of hepatitis B virus core protein in viral replication

被引:129
作者
Lan, YT [1 ]
Li, J [1 ]
Liao, WY [1 ]
Ou, JH [1 ]
机构
[1] Univ So Calif, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1006/viro.1999.9798
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Hepatitis B virus (HBV) core protein is a phosphoprotein. Its three major phosphorylation sites have been identified at the serine residues located at amino acids 157, 164, and 172. In order to investigate the role of core protein phosphorylation in HBV replication, these three serine residues were mutated to alanine to mimic nonphosphorylated serine or to glutamic acid to mimic phosphoserine. The nonphosphorylated core protein analog did not package the HBV pregenomic RNA, and the phosphorylated analog packaged the pregenomic RNA but failed to support viral DNA replication. These results indicate that the core protein phosphorylation may be important for pregenomic RNA packaging and that its dephosphorylation may be important for viral DNA replication. The individual roles of these three major phosphorylation sites in HBV replication were further investigated by being mutated to alanine in different combinations. The results showed that the serine residue at amino acid 157 was not essential for pregenomic RNA packaging, whereas the serine residues at amino acids 164 and 172 were more important Furthermore, the serine residue at amino acid 157 was not essential for viral DNA replication or viral maturation. (C) 1999 Academic Press.
引用
收藏
页码:342 / 348
页数:7
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