Hashimoto S, Pursley M H, Green M
Nucleic Acids Res. 1981 Apr 10;9(7):1675-89. doi: 10.1093/nar/9.7.1675.
The major 5'-termini of human adenovirus type 2 early gene block 4 mRNA were sequenced. Poly(A+) polyribosomal RNA was isolated from Ad2 early infected cells, the 5'-terminal m7GPPP removed and the 5'-OH of the penultimate 2'-0-methylated nucleotide labeled with [gamma-32P]ATP using polynucleotide kinase. Ad2 E4 mRNA was purified by hybridization to the Ad2 EcoRI-C fragment and was digested with RNase T1. The resulting oligonucleotides were resolved by two dimensional paper electrophoresis-homochromatography. Four major and 3-4 minor 5'-terminal sequences were identified and characterized. The sequence of the 5'-terminal structures of the major four termini are: (1) m7GpppUmU(m)UUACACUGp, (2) m7GpppUmU(m)UACACUGp, (3) m7GpppUmU(m)ACACUGp, and (4) m7Gppp(m6)AmC(m)ACUGp. These major 5'-terminal sequences were aligned with nucleotide 325, 326, 327, and 329 from the righthand end of the known Ad2 DNA sequence (1) in the region mapped as the 5'-terminus of E4 mRNA by electron microscopy (2,3) and S1 nuclease-gel (4) mapping. Two potential ribosomal binding sites and an initiator codon were found at 40 to 65 nucleotides and about 80 nucleotides, respectively, from these heterogenous 5'-termini. Ad2 E4 major mRNA species appear to be unique since mRNA molecules initiate at a pyrimidine, perhaps by RNA polymerase stuttering, or they are products of an unusual type of RNA processing.
对人2型腺病毒早期基因阻断区4(E4)mRNA的主要5′末端进行了测序。从腺病毒2型(Ad2)早期感染的细胞中分离出聚腺苷酸[poly(A+)]多核糖体RNA,去除5′末端的m7GPPP,使用多核苷酸激酶将倒数第二个2′-O-甲基化核苷酸的5′-OH用[γ-32P]ATP进行标记。Ad2 E4 mRNA通过与Ad2 EcoRI-C片段杂交进行纯化,并用核糖核酸酶T1进行消化。所得的寡核苷酸通过二维纸电泳-同系层析进行分离。鉴定并表征了四个主要的和3 - 4个次要的5′末端序列。四个主要末端的5′末端结构序列如下:(1) m7GpppUmU(m)UUACACUGp,(2) m7GpppUmU(m)UACACUGp,(3) m7GpppUmU(m)ACACUGp,以及(4) m7Gppp(m6)AmC(m)ACUGp。这些主要的5′末端序列与已知Ad2 DNA序列(1)右端的第325、326、327和329位核苷酸进行比对,该区域通过电子显微镜(2,3)和S1核酸酶-凝胶(4)图谱分析被定位为E4 mRNA的5′末端。从这些异质性的5′末端分别在40至65个核苷酸和约80个核苷酸处发现了两个潜在的核糖体结合位点和一个起始密码子。Ad2 E4主要mRNA种类似乎是独特的,因为mRNA分子从嘧啶起始,可能是通过RNA聚合酶的打滑,或者它们是一种不寻常类型的RNA加工的产物。