Price P M, Mohamad A, Zelent A, Neurath A R, Acs G
Department of Biochemistry, Mount Sinai School of Medicine, New York, NY 10029.
DNA. 1988 Jul-Aug;7(6):417-22. doi: 10.1089/dna.1.1988.7.417.
The region of the hepatitis B virus (HBV) genome coding for the viral envelope proteins contains three inphase ATGs that are conserved among viral subtypes. Each of these ATGs can be used as mRNA initiation codons. The three translated proteins share a carboxy-terminal region (the S protein) and extend amino-terminally to include the pre-S2 region in the middle (M) protein, and the pre-S1 and pre-S2 regions in the large (L) protein. We have inserted the HBV DNA coding for the M protein into a baculovirus expression vector. Infected insect cells transcribe a mRNA that is initiated solely within a baculovirus promoter, and that contains the initiator codons for both M and S proteins. Although these cells primarily secrete the M protein, the major translational product is the S protein, which is not secreted. This preferential translation, the result of the use of an internal initiator codon, demonstrates that the regulation of HBV envelope protein production can occur at the translational level.
乙型肝炎病毒(HBV)基因组中编码病毒包膜蛋白的区域含有三个同相位的ATG,这些ATG在病毒亚型中是保守的。这些ATG中的每一个都可以用作mRNA起始密码子。这三种翻译产物共享一个羧基末端区域(S蛋白),并在氨基末端延伸,中间蛋白(M蛋白)包含前S2区域,大蛋白(L蛋白)包含前S1和前S2区域。我们已将编码M蛋白的HBV DNA插入杆状病毒表达载体中。被感染的昆虫细胞转录出一种mRNA,该mRNA仅在杆状病毒启动子内起始,并且包含M蛋白和S蛋白的起始密码子。尽管这些细胞主要分泌M蛋白,但主要翻译产物却是不分泌的S蛋白。这种优先翻译是使用内部起始密码子的结果,表明HBV包膜蛋白产生的调节可发生在翻译水平。