Tigges M A, Raskas H J
J Virol. 1984 Apr;50(1):106-17. doi: 10.1128/JVI.50.1.106-117.1984.
We localized the splice junctions in adenovirus 2 early region 4 (E4) mRNAs. Processing of the E4 precursor RNA positioned the donor splice site of the 5' leader sequence adjacent to acceptor sites near the 5' ends of five of the six open reading regions in the E4 transcription unit. Of particular interest among the E4 mRNAs is an extensively spliced class which includes multiple species with sizes ranging from 1.1 to 0.75 kilobases (kb). Purified 1.1- to 0.75-kb mRNAs specified at least 10 polypeptides in vitro. We detected eight acceptor and two donor splice sites utilized in the deletion of the intron from the 3' portion of these mRNAs. E4 RNAs were isolated from the cytoplasm of infected cells at 5, 9, 12, and 18 h after infection. The E4 mRNAs were present throughout infection, but different members of the 1.1- to 0.7-kb class were predominant at each time assayed. Alternate splicing of the 3.0-kb E4 precursor RNA can generate as many as 25 mRNAs that encode at least 16 polypeptides.
我们对腺病毒2型早期区域4(E4)mRNA中的剪接位点进行了定位。E4前体RNA的加工过程使得5'前导序列的供体剪接位点与E4转录单元中六个开放阅读框中五个的5'端附近的受体位点相邻。在E4 mRNA中,特别引人关注的是一类经过广泛剪接的mRNA,其中包括多种大小在1.1至0.75千碱基(kb)之间的mRNA。纯化后的1.1至0.75 kb的mRNA在体外至少能编码10种多肽。我们检测到在这些mRNA的3'部分内含子缺失过程中使用了8个受体剪接位点和2个供体剪接位点。在感染后5、9、12和18小时从感染细胞的细胞质中分离出E4 RNA。在整个感染过程中都存在E4 mRNA,但在每次检测时,1.1至0.7 kb类别的不同成员占主导地位。3.0 kb E4前体RNA的可变剪接可产生多达25种mRNA,这些mRNA至少编码16种多肽。