Jenh C H, Deng T L, Li D W, DeWille J, Johnson L F
Proc Natl Acad Sci U S A. 1986 Nov;83(22):8482-6. doi: 10.1073/pnas.83.22.8482.
Analysis of the sequence of cDNA corresponding to mouse thymidylate synthase (5,10-methylenetetrahydrofolate:dUMP C-methyltransferase, EC 2.1.1.45) mRNA revealed that the termination codon TAA was followed immediately by a poly(A) sequence. This raised the possibility that mouse thymidylate synthase mRNA lacks a 3' untranslated region. In the present study, we have further investigated this possibility. DNA corresponding to the 3' end of the thymidylate synthase gene was isolated from a genomic library. The sequence of the genomic DNA was identical to that of the cDNA in the coding region. However, the termination codon was TAG in the genomic sequence rather than TAA, and poly(A) was not present in the genomic DNA. Sequences flanking the site of poly(A) addition were in good agreement with polyadenylylation consensus sequences. S1 nuclease analysis revealed that approximately 80% of the thymidylate synthase mRNA molecules were polyadenylylated at the termination codon. A secondary polyadenylylation site was detected 190-200 nucleotides downstream of the primary site. We conclude that the major species of mouse thymidylate synthase mRNA lacks a 3' untranslated region and that the final A of the termination codon is added by poly(A) polymerase. It appears that a 3' untranslated region is not essential for the accumulation or translation of this mRNA.
对与小鼠胸苷酸合成酶(5,10-亚甲基四氢叶酸:dUMP C-甲基转移酶,EC 2.1.1.45)mRNA相对应的cDNA序列分析显示,终止密码子TAA之后紧接着是一个聚腺苷酸序列。这就提出了小鼠胸苷酸合成酶mRNA缺乏3'非翻译区的可能性。在本研究中,我们进一步研究了这种可能性。从基因组文库中分离出与胸苷酸合成酶基因3'端相对应的DNA。基因组DNA的序列在编码区与cDNA的序列相同。然而,基因组序列中的终止密码子是TAG而不是TAA,并且基因组DNA中不存在聚腺苷酸。聚腺苷酸添加位点两侧的序列与聚腺苷酸化共有序列高度一致。S1核酸酶分析显示,约80%的胸苷酸合成酶mRNA分子在终止密码子处进行了聚腺苷酸化。在主要位点下游190 - 200个核苷酸处检测到一个次要的聚腺苷酸化位点。我们得出结论,小鼠胸苷酸合成酶mRNA的主要种类缺乏3'非翻译区,并且终止密码子的最后一个A是由聚腺苷酸聚合酶添加的。看来3'非翻译区对于这种mRNA的积累或翻译并非必不可少。