Passarelli A L, Miller L K
Department of Genetics, University of Georgia, Athens 30602.
Virology. 1993 Dec;197(2):704-14. doi: 10.1006/viro.1993.1646.
Using a previously developed method that allows the identification of Autographa californica nuclear polyhedrosis virus (AcMNPV) genes which stimulate transient expression from a late and a very late viral promoter [Passarelli and Miller, J. Virol., 67, 2149-2158 (1993)], we have identified three genes between 56.0 and 65.4 map units of the AcMNPV genome involved in expression from a late and a very late promoter but not from an early viral promoter. One gene, p143, was previously shown to be essential for viral DNA replication and shares sequence motifs with DNA helicases [Lu and Carstens, Virology, 181, 336-347 (1991)]. The second gene, previously sequenced and originally referred to as open reading frame 6 (herein renamed late expression factor-5 [lef-5]), was located just downstream of the 6.9 kilodalton core protein gene, p6.9. The third gene, late expression factor-4 (lef-4), was defined and sequenced. The lef-4 gene was located immediately upstream of, and in opposite orientation to, the major capsid protein gene, vp39. The position and direction of lef-4 appeared to be conserved in the Orgyia pseudotsugata and Lymantria dispar nuclear polyhedrosis viruses. The gene product of lef-4, LEF-4, is predicted to be an acidic polypeptide (pl 4.91) of 464 amino acids in length with a molecular mass of 53,913 daltons.
利用一种先前开发的方法,该方法能够鉴定出刺激晚期和极晚期病毒启动子瞬时表达的苜蓿银纹夜蛾核型多角体病毒(AcMNPV)基因[帕萨雷利和米勒,《病毒学杂志》,67卷,2149 - 2158页(1993年)],我们在AcMNPV基因组56.0至65.4个图谱单位之间鉴定出三个基因,它们参与晚期和极晚期启动子的表达,但不参与早期病毒启动子的表达。一个基因,p143,先前已证明对病毒DNA复制至关重要,并且与DNA解旋酶共享序列基序[卢和卡斯滕斯,《病毒学》,181卷,336 - 347页(1991年)]。第二个基因,先前已测序,最初称为开放阅读框6(在此重新命名为晚期表达因子 - 5 [lef - 5]),位于分子量6.9千道尔顿的核心蛋白基因p6.9的下游。第三个基因,晚期表达因子 - 4(lef - 4),已被确定并测序。lef - 4基因位于主要衣壳蛋白基因vp39的紧邻上游,且方向相反。lef - 4的位置和方向在云杉毒蛾和舞毒蛾核型多角体病毒中似乎是保守的。lef - 4的基因产物LEF - 4预计是一种酸性多肽(等电点4.91),长度为464个氨基酸,分子量为53,913道尔顿。