Redmond S M, Dickson C
Imperial Cancer Research Fund Laboratories, London, UK.
EMBO J. 1983;2(1):125-31. doi: 10.1002/j.1460-2075.1983.tb01393.x.
We have determined the DNA sequence of the envelope gene region of the GR strain of mouse mammary tumour virus. The sequence extends for 3012 nucleotides from the single EcoRI site to beyond the PstI site in the 3' long terminal repeat (LTR) of the provirus. There is a major open reading frame from nucleotides 752 to 2818 which encompasses the entire env gene. This reading frame extends through a polypurine tract and into the LTR. There is another open reading frame from the first nucleotide to position 803, presumably corresponding to the end of the pol gene. The splice acceptor site which generates env mRNA has been mapped experimentally to nucleotide 750. The env gene products, gp52 and gp36, have been positioned on the sequence using the directly determined amino acid sequences of the amino terminus of gp52; and both the amino and carboxyl termini of gp36. The start of gp52 is preceded by a series of 19 uncharged amino acids which could function as a typical signal sequence, but this sequence is only part of a much longer leader peptide. The tetrad Arg-Ala-Lys-Arg is the presumed cleavage site in the gPr73env precursor, and occurs just before the gp36 amino terminus. There are five potential asparagine-linked glycosylation sites which agrees with previous experimental results. The gp36 has two long hydrophobic regions at its amino and carboxy termini, these are suggested to act as a fusion peptide and the trans-membrane anchor, respectively.
我们已经测定了小鼠乳腺肿瘤病毒GR株包膜基因区域的DNA序列。该序列从前病毒3'长末端重复序列(LTR)中的单个EcoRI位点延伸3012个核苷酸至PstI位点之外。从核苷酸752到2818有一个主要的开放阅读框,它包含了整个env基因。这个阅读框延伸穿过一个多聚嘌呤序列并进入LTR。从第一个核苷酸到第803位还有另一个开放阅读框,推测对应于pol基因的末端。通过实验已将产生env mRNA的剪接受体位点定位到核苷酸750。利用直接测定的gp52氨基末端以及gp36氨基和羧基末端的氨基酸序列,已将env基因产物gp52和gp36定位在该序列上。gp52的起始位点之前有一系列19个不带电荷的氨基酸,它们可能起典型信号序列的作用,但该序列只是一个长得多的前导肽的一部分。四联体精氨酸 - 丙氨酸 - 赖氨酸 - 精氨酸是推测的gPr73env前体中的切割位点,恰好在gp36氨基末端之前。有五个潜在的天冬酰胺连接的糖基化位点,这与先前的实验结果一致。gp36在其氨基和羧基末端有两个长的疏水区域,分别被认为起融合肽和跨膜锚定的作用。