Salmons B, Knedlitschek G, Kennedy N, Groner B, Ponta H
Virus Res. 1986 Jun;4(4):377-89. doi: 10.1016/0168-1702(86)90084-5.
The Mtv-8 associated provirus, GR40, is not expressed in vivo. However, upon transfection into rat XC cells, the two MMTV specific mRNAs of 35S and 24S are transcribed. Further, the level of these transcripts is augmented when the transfected cells are grown in the presence of dexamethasone (Ponta et al., 1983). No virus can be detected in the medium of the transfected cells. Intracellular protein analysis of these transfected cells shows that although apparently authentic gag proteins are synthesized, a novel protein of 68 kDa is the only env related protein detectable. The sequence of the env gene of GR40 was determined and the predicted amino acid sequence of the env protein obtained. A premature termination codon is present 68 amino acids before the COOH-terminus of the known MMTV env precursor Pr73env. This would result in an env protein of about 68 kDa, in agreement with the size of the env protein found in GR40 transfected cells. The lack of the carboxy terminus may be responsible for the non-processing of the aberrant env precursor protein, p68.
与Mtv - 8相关的前病毒GR40在体内不表达。然而,转染到大鼠XC细胞后,会转录出35S和24S这两种MMTV特异性mRNA。此外,当转染细胞在存在地塞米松的情况下生长时,这些转录本的水平会增加(庞塔等人,1983年)。在转染细胞的培养基中未检测到病毒。对这些转染细胞进行的细胞内蛋白质分析表明,虽然显然合成了正宗的gag蛋白,但68 kDa的一种新蛋白是唯一可检测到的与env相关的蛋白。测定了GR40的env基因序列并获得了env蛋白的预测氨基酸序列。在已知的MMTV env前体Pr73env的COOH末端前68个氨基酸处存在一个过早的终止密码子。这将导致产生一种约68 kDa的env蛋白,这与在GR40转染细胞中发现的env蛋白大小一致。羧基末端的缺失可能是异常env前体蛋白p68未被加工的原因。