Flomenberg P R, Chen M, Horwitz M S
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461.
J Virol. 1988 Nov;62(11):4431-7. doi: 10.1128/JVI.62.11.4431-4437.1988.
The early transcription region 3 (E3) of group B adenovirus type 35 (Ad35), a serotype isolated primarily from patients with acquired immunodeficiency syndrome and other immunodeficiency disorders, has been partially sequenced. We had previously identified an Ad35 29-kilodalton (kDa) early glycoprotein which, analogous to group C Ad2 E3-19K, associated with major histocompatibility complex class I antigens in the endoplasmic reticulum of infected cells. The open reading frame (ORF) of the Ad35 29-kDa protein has now been identified within a 2-kilobase-pair cloned Ad35 E3 fragment. The predicted amino acid sequence was very similar to that of group B Ad3 E3-19K. In contrast, homology between the Ad35 and Ad2 glycoproteins was limited to five cysteines in identical positions and a 20-amino-acid region proximal to the transmembrane domain. In addition, 20.3- and 20.6-kDa ORFs have been identified downstream from the ORF for the Ad35 glycoprotein. Analogous 20-kDa ORFs are present in the Ad3 E3 region but are not present in Ad2 and Ad5. In contrast, the region analogous to an Ad2 11.6-kDa ORF, which is 9 kDa in size in Ad3, was absent from the expected position within the Ad35 E3 region. Because the E3 region is likely to play an important role in the interaction between virus and host, analysis of the function of the Ad35 E3 proteins should further our understanding of adenovirus pathogenesis.
35型B组腺病毒(Ad35)的早期转录区3(E3)已被部分测序,该血清型主要从获得性免疫缺陷综合征患者和其他免疫缺陷疾病患者中分离得到。我们之前鉴定出一种Ad35 29千道尔顿(kDa)的早期糖蛋白,它与C组Ad2 E3-19K类似,在受感染细胞的内质网中与主要组织相容性复合体I类抗原相关联。现在,已在一个2千碱基对的克隆Ad35 E3片段中鉴定出Ad35 29-kDa蛋白的开放阅读框(ORF)。预测的氨基酸序列与B组Ad3 E3-19K的序列非常相似。相比之下,Ad35和Ad2糖蛋白之间的同源性仅限于相同位置的五个半胱氨酸以及跨膜结构域近端的一个20个氨基酸的区域。此外,在Ad35糖蛋白的ORF下游还鉴定出了20.3-kDa和20.6-kDa的ORF。Ad3 E3区域中存在类似的20-kDa ORF,但Ad2和Ad5中不存在。相反,Ad35 E3区域中预期位置缺少与Ad2 11.6-kDa ORF类似的区域,该区域在Ad3中大小为9 kDa。由于E3区域可能在病毒与宿主之间的相互作用中发挥重要作用,对Ad35 E3蛋白功能的分析应能增进我们对腺病毒发病机制的理解。