Takeshima H, Inokoshi J, Namiki M, Shimada J, Omura S
J Gen Virol. 1985 Jan;66 ( Pt 1):195-200. doi: 10.1099/0022-1317-66-1-195.
The entire genome of hepatitis B virus (subtype adr) has been cloned into pBR322. The clones could be classified into at least seven groups by their restriction endonuclease cleavage maps. The nucleotide sequences of the hepatitis B surface antigen (HBsAg)-coding regions for five clones were determined and compared with published sequences of the HBsAg gene including those of adw, ayw, adyw and adr. The 13 available versions of the amino acid sequence of the polypeptide, predicted from the nucleotide sequences, were analysed in terms of the established specificities of the HBsAg, including the four subtypes. The analysis indicated that a relatively hydrophilic region of the HBsAg protein, spanning amino acid residues 110 to 160, specifies the major (w) and (r) subtype system. The (w/r) subtype appears to depend on changes in one or more variable amino acids at positions 47, 110, 113, 126 and 160 of the HBsAg polypeptide.
乙型肝炎病毒(adr亚型)的全基因组已被克隆到pBR322中。这些克隆可根据其限制性内切酶切割图谱分为至少七组。测定了五个克隆的乙型肝炎表面抗原(HBsAg)编码区的核苷酸序列,并与已发表的HBsAg基因序列进行比较,这些序列包括adw、ayw、adyw和adr的序列。根据核苷酸序列预测的该多肽的13种可用氨基酸序列版本,按照已确定的HBsAg特异性进行分析,包括四种亚型。分析表明,HBsAg蛋白中一个相对亲水的区域,跨越氨基酸残基110至160,决定了主要的(w)和(r)亚型系统。(w/r)亚型似乎取决于HBsAg多肽第47、110、113、126和160位一个或多个可变氨基酸的变化。