Gorman Jeffrey J, Wallis Tristan P, Whelan Dean A, Shaw Jan, Both Gerald W
Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Virology. 2005 Nov 10;342(1):159-66. doi: 10.1016/j.virol.2005.07.020. Epub 2005 Aug 19.
Ovine adenovirus serotype 7 (OAdV), the prototype atadenovirus, has gene homologues for most mastadenovirus structural proteins but lacks proteins V and IX. Instead, OAdV has structural proteins of 32 and 42 kDa although the gene encoding the latter had not previously been identified. The presently reported studies of OAdV virions have now identified a minor structural polypeptide of approximately 40 kDa as the product of the L1 52/55-kDa gene and, more surprisingly, shown that the 42-kDa protein is encoded by LH3. This gene product was previously thought to be a homologue of mastadenovirus E1B 55 kDa, which is a multi-functional, non-structural protein that cooperates with E1A in cell transformation. The lack of transforming activity previously demonstrated for OAdV combined with a structural role for the LH3 product indicates that the protein has a different function in atadenoviruses. We discuss the abundance and likely core location of LH3 in the virion and the possible derivation of the E1B 55-kDa gene from the LH3 gene.
绵羊腺病毒7型(OAdV)是腺联病毒的原型,它具有大多数哺乳动物腺病毒结构蛋白的基因同源物,但缺乏蛋白V和IX。相反,OAdV具有32 kDa和42 kDa的结构蛋白,尽管之前尚未鉴定出编码后者的基因。目前关于OAdV病毒粒子的研究现已确定一种约40 kDa的次要结构多肽是L1 52/55-kDa基因的产物,更令人惊讶的是,表明42-kDa蛋白由LH3编码。该基因产物以前被认为是哺乳动物腺病毒E1B 55 kDa的同源物,E1B 55 kDa是一种多功能非结构蛋白,在细胞转化中与E1A协同作用。先前证明OAdV缺乏转化活性,结合LH3产物的结构作用,表明该蛋白在腺联病毒中具有不同功能。我们讨论了LH3在病毒粒子中的丰度和可能的核心位置,以及E1B 55-kDa基因可能从LH3基因衍生而来。