Robertson D L
J Virol. 1984 May;50(2):632-5. doi: 10.1128/JVI.50.2.632-635.1984.
The kinetics of dexamethasone induction of mouse mammary tumor virus RNAs in a cell line (designated line 8) which contains a deleted proviral DNA has been examined. This DNA is an apparent reverse transcription product of the env mRNA. A detectable increase in the 3.8-kilobase RNA (mouse mammary tumor virus env mRNA) was present within 15 min after hormone addition. The 2.5-kilobase RNA detected previously during hormone induction studies was also observed in these cells. Both RNAs increased in concentration up to about 4 h after hormone addition and thereafter attained the steady-state level. Pr73env was detected by immunoprecipitation and appeared to be identical to bona fide Pr73env isolated from wild-type mouse mammary tumor virus-infected cells. An additional 5.7 kilobases of RNA was detected in augmented quantities after hormone addition, but the structure of this RNA is not known.
已对含有缺失前病毒DNA的细胞系(命名为8号线)中地塞米松诱导小鼠乳腺肿瘤病毒RNA的动力学进行了研究。该DNA是env mRNA的明显逆转录产物。添加激素后15分钟内,3.8千碱基RNA(小鼠乳腺肿瘤病毒env mRNA)出现可检测到的增加。在这些细胞中也观察到了先前在激素诱导研究中检测到的2.5千碱基RNA。两种RNA的浓度在添加激素后约4小时内都有所增加,此后达到稳态水平。通过免疫沉淀检测到Pr73env,并且它似乎与从野生型小鼠乳腺肿瘤病毒感染细胞中分离出的真正Pr73env相同。添加激素后,还检测到另外5.7千碱基的RNA数量增加,但这种RNA的结构尚不清楚。