Lenz J, Crowther R, Straceski A, Haseltine W
J Virol. 1982 May;42(2):519-29. doi: 10.1128/JVI.42.2.519-529.1982.
The sequence of 2,191 nucleotides encoding the env gene of murine retrovirus Akv was determined by using a molecular clone of the Akv provirus. Deduction of the encoded amino acid sequence showed that a single open reading frame encodes a 638-amino acid precursor to gp70 and p15E. In addition, there is a typical leader sequence preceding the amino terminus of gp70. The locations of potential glycosylation sites and other structural features indicate that the entire gp70 molecule and most of p15E are located on the outer side of the membrane. Internal cleavage of the env precursor to generate gp70 and p15E occurs immediately adjacent to several basic amino acids at the carboxyl terminus of gp70. This cleavage generates a region of 42 uncharged, relatively hydrophobic amino acids at the amino terminus of p15E, which is located in a position analogous to the hydrophobic membrane fusion sequence of influenza virus hemagglutinin. The mature polypeptides are predicted to associate with the membrane via a region of 30 uncharged, mostly hydrophobic amino acids located near the carboxyl terminus of p15E. Distal to this membrane association region is a sequence of 35 amino acids at the carboxyl terminus of the env precursor, which is predicted to be located on the inner side of the membrane. By analogy to Moloney murine leukemia virus, a proteolytic cleavage in this region removes the terminal 19 amino acids, thus generating the carboxyl terminus of p15E. This leaves 15 amino acids at the carboxyl terminus of p15E on the inner side of the membrane in a position to interact with virion cores during budding. The precise location and order of the large RNase T(1)-resistant oligonucleotides in the env region were determined and compared with those from several leukemogenic viruses of AKR origin. This permitted a determination of how the differences in the leukemogenic viruses affect the primary structure of the env gene products.
利用Akv前病毒的分子克隆,确定了编码鼠逆转录病毒Akv env基因的2191个核苷酸的序列。推导的编码氨基酸序列表明,一个单一的开放阅读框编码gp70和p15E的638个氨基酸前体。此外,在gp70氨基末端之前有一个典型的前导序列。潜在糖基化位点的位置和其他结构特征表明,整个gp70分子和大部分p15E位于膜的外侧。env前体内部切割产生gp70和p15E,切割发生在gp70羧基末端的几个碱性氨基酸紧邻处。这种切割在p15E的氨基末端产生了一个由42个不带电荷、相对疏水的氨基酸组成的区域,该区域位于与流感病毒血凝素的疏水膜融合序列类似的位置。预测成熟多肽通过位于p15E羧基末端附近的30个不带电荷、大多为疏水的氨基酸区域与膜结合。在这个膜结合区域的远端是env前体羧基末端的35个氨基酸序列,预计位于膜的内侧。与莫洛尼鼠白血病病毒类似,该区域的蛋白水解切割去除了末端的19个氨基酸,从而产生了p15E的羧基末端。这使得p15E羧基末端的15个氨基酸位于膜内侧,在出芽过程中能够与病毒核心相互作用。确定了env区域中对核糖核酸酶T(1)有抗性的大寡核苷酸的精确位置和顺序,并与几种源自AKR的致白血病病毒的进行了比较。这使得能够确定致白血病病毒中的差异如何影响env基因产物的一级结构。