Keene J D, Schubert M, Lazzarini R A
J Virol. 1980 Feb;33(2):789-94. doi: 10.1128/JVI.33.2.789-794.1980.
The base sequence at the 3' end of vesicular stomatitis virus RNA was determined by using terminal labels and chemical RNA sequencing. The leader RNA was complementary to 47 bases at the 3' terminus, whereas the nucleocapsid gene (N) began 51 nucleotides from the 3' end of the genomic RNA. The intervening bases were 3'...GAAA...5' for the Indiana serotype and 3'...GAAAA...5' for the New Jersey serotype. The complements of these bases did not appear in either the leader RNA or the N mRNA. This sequence may function as a stop signal or cleavage site during transcription. Furthermore, processing or termination at this sequence must be inhibited during the production of full-length RNA plus-sense strands (replication). We recently found similar sequences approximately 46 to 48 nucleotides from the 3' ends of several defective interfering particle RNAs where the short defective interfering particle transciption products terminate. This sequence is present also at the end of the polymerase (L) gene.
通过使用末端标记和化学RNA测序确定了水疱性口炎病毒RNA 3'端的碱基序列。前导RNA与3'末端的47个碱基互补,而核衣壳基因(N)从基因组RNA的3'端开始51个核苷酸处起始。印第安纳血清型的间隔碱基为3'...GAAA...5',新泽西血清型的为3'...GAAAA...5'。这些碱基的互补序列在引导RNA或N mRNA中均未出现。该序列可能在转录过程中充当终止信号或切割位点。此外,在全长RNA正链(复制)产生过程中,必须抑制在此序列处的加工或终止。我们最近在几种缺陷干扰颗粒RNA的3'端约46至48个核苷酸处发现了类似序列,短缺陷干扰颗粒转录产物在此处终止。该序列也存在于聚合酶(L)基因的末端。