Canaani D, Kahana C, Lavi S, Groner Y
Nucleic Acids Res. 1979 Jun 25;6(8):2879-99. doi: 10.1093/nar/6.8.2879.
Late SV40 16S and 19S mRNAs were found to contain an average of three m6A residues per mRNA molecule. The methylated residues of both the viral and cellular mRNAs occur in two sequences; Gpm6ApC and (Ap)nm6ApC, where n = 1-4. More than 60% of the m6A residues in SV40 16S and 19S mRNAs occur in Gpm6ApC even though there are twice as many (A)nAC than GAC sequences in these messengers. The m6A containing oligonucleotides of late SV40 MRNAs were localized in the viral messengers. In the 16S mRNA two m6A oligonucleotides were located at the 5' coding region between 0.95--0.0 map units. The third m6A residue was mapped between 0.0--0.14 map units in the translated portion of this mRNA. The overall pattern of internal methylation in the 19S mRNA is similar. However, some differences between 16S and 19S mRNAs were observed in both the content and location of the longer (Ap)n m6AC nucleotides. These results provide the first example of precise localization of internal methylation sequences in mRNA species with defined coding specificity. It implies that a) location of m6A residues is not random but specific to a particular region of the RNA, b) apart from sequence specificity other structural features of the mRNA may influence internal methylation and c) m6A residues are present in coding regions of SV40 mRNAs.
研究发现,SV40晚期16S和19S mRNA平均每个mRNA分子含有三个m6A残基。病毒mRNA和细胞mRNA的甲基化残基均出现在两种序列中:Gpm6ApC和(Ap)nm6ApC,其中n = 1 - 4。尽管在这些信使RNA中(A)nAC序列的数量是GAC序列的两倍,但SV40 16S和19S mRNA中超过60%的m6A残基出现在Gpm6ApC中。晚期SV40 mRNA含m6A的寡核苷酸定位于病毒信使RNA中。在16S mRNA中,两个m6A寡核苷酸位于5'编码区0.95 - 0.0图谱单位之间。第三个m6A残基位于该mRNA翻译部分的0.0 - 0.14图谱单位之间。19S mRNA内部甲基化的总体模式与之相似。然而,在较长的(Ap)n m6AC核苷酸的含量和位置方面,16S和19S mRNA之间存在一些差异。这些结果首次给出了具有明确编码特异性的mRNA物种内部甲基化序列精确定位的实例。这意味着:a) m6A残基的位置不是随机的,而是特定于RNA的特定区域;b) 除了序列特异性外,mRNA的其他结构特征可能会影响内部甲基化;c) m6A残基存在于SV40 mRNA的编码区。