Cohen M, Powers M, O'Connell C, Kato N
Virology. 1985 Dec;147(2):449-58. doi: 10.1016/0042-6822(85)90147-3.
The nucleotide sequence of the env gene of a previously described human provirus (ERV3) has been determined beginning near the 3'-end of the pol gene and continuing through the 3'-LTR. Analysis of the nucleotide sequence revealed the presence of a long open reading frame of 1944 nucleotides that is capable of encoding a polypeptide that has characteristics of other retroviral glycoproteins and transmembrane proteins. These include the presence of seven potential glycosylation sites, a typical glycoprotein-transmembrane protein cleavage sequence, and amino acid homologies to the glycoproteins and transmembrane proteins of other retroviruses. Further, we have isolated an ERV3-specific cDNA clone from a library prepared from liver RNA of a 20-week human fetus. DNA sequence analysis of this clone revealed that it is identical to the ERV3 genomic clone in the 1110 nucleotides that were sequenced.
一个先前描述的人类前病毒(ERV3)的env基因核苷酸序列已被确定,起始于pol基因的3'端附近,并延伸至3'-LTR。核苷酸序列分析显示存在一个1944个核苷酸的长开放阅读框,其能够编码一种具有其他逆转录病毒糖蛋白和跨膜蛋白特征的多肽。这些特征包括七个潜在的糖基化位点、一个典型的糖蛋白-跨膜蛋白切割序列,以及与其他逆转录病毒的糖蛋白和跨膜蛋白的氨基酸同源性。此外,我们从一个由20周龄人类胎儿肝脏RNA制备的文库中分离出了一个ERV3特异性cDNA克隆。对该克隆的DNA序列分析表明,在测序的1110个核苷酸中,它与ERV3基因组克隆相同。