Sherman L, Levanon D, Lieman-Hurwitz J, Dafni N, Groner Y
Nucleic Acids Res. 1984 Dec 21;12(24):9349-65. doi: 10.1093/nar/12.24.9349.
Two cytoplasmic superoxide dismutase (SOD-1) mRNAs of about 0.7 and 0.9 kilobases (Kb.) were previously found in a variety of human cells. The two SOD-1 mRNAs are transcribed from the same gene and the major 0.7 Kb. species is approximately four times more abundant than the minor 0.9 Kb. mRNA. These two mRNAs differ in the length of their 3'-untranslated region and both have multiple 5'-ends. The longer transcript contains 222 additional nucleotides beyond the 3'-polyadenylated terminus of the short mRNA. S1 nuclease mapping and sequence analysis showed that these extra 222 nucleotides are specified by sequences contiguous to those shared by the two SOD-1 mRNAs. The 5'-termini of the two SOD-1 mRNAs were identified and mapped by both primer extension and S1 mapping. The majority of SOD-1 mRNA molecules (90-95%) have a 5'-start site located 23 base pairs (b.p.) downstream of the hexanucleotide -TATAAA-. The rest of the SOD-1 mRNA molecules have 5'-termini 30, 50 and 65 b.p. upstream from the major start region.
先前在多种人类细胞中发现了两种大小约为0.7和0.9千碱基(Kb.)的细胞质超氧化物歧化酶(SOD-1)mRNA。这两种SOD-1 mRNA由同一个基因转录而来,其中主要的0.7 Kb.种类的丰度大约是次要的0.9 Kb. mRNA的四倍。这两种mRNA的3'-非翻译区长度不同,且都有多个5'-末端。较长的转录本在短mRNA的3'-聚腺苷酸化末端之外还包含222个额外的核苷酸。S1核酸酶图谱分析和序列分析表明,这额外的222个核苷酸由与两种SOD-1 mRNA共享的序列相邻的序列所指定。通过引物延伸和S1图谱分析鉴定并定位了两种SOD-1 mRNA的5'-末端。大多数SOD-1 mRNA分子(90-95%)的5'-起始位点位于六核苷酸-TATAAA-下游23个碱基对(b.p.)处。其余的SOD-1 mRNA分子的5'-末端位于主要起始区域上游30、50和65个碱基对处。