Trávnícek M, Frolova L Y, Ríman J
J Gen Virol. 1976 Feb;30(2):187-95. doi: 10.1099/0022-1317-30-2-187.
Controlled disruption of 60S AMV RNA with formamide was used to prepare 50-55S and 30-40S RNAS. When the activities of these RNAs as templates for AMV reverse transcriptase were compared it was found that 50-55S RNA was 1-5 times and 30-40S RNA 2 to 3 times more active than 60S RNA. The 30-40S RNA produced by heating, instead of formamide disruption, was inactive as a template but activity was restored by addition of oligo(dT). 40% of the 4S RNA initially associated with the 60S RNA remained associated with all the RNA species obtained by formamide treatment but was lost on heating. It is concluded that this RNA acts as resident primer whereas the other 60% of the 4S RNA is less firmly bound and appears to have little or no primer activity. Removal of the less firmly bound 4S RNA increases the template activity of the viral RNA.
用甲酰胺对60S禽成髓细胞瘤病毒(AMV)RNA进行可控切割,以制备50 - 55S和30 - 40S RNA。当比较这些RNA作为AMV逆转录酶模板的活性时,发现50 - 55S RNA的活性比60S RNA高1 - 5倍,30 - 40S RNA的活性比60S RNA高2至3倍。通过加热而非甲酰胺切割产生的30 - 40S RNA作为模板无活性,但添加寡聚(dT)后活性得以恢复。最初与60S RNA结合的4S RNA中,40%仍与通过甲酰胺处理获得的所有RNA种类结合,但加热时会丢失。结论是,这种RNA作为常驻引物,而另外60%的4S RNA结合较不牢固,似乎几乎没有引物活性。去除结合较不牢固的4S RNA可提高病毒RNA的模板活性。