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由GAC突变为GAU导致的两个内部N6-甲基腺苷位点甲基化的抑制。

Inhibition of methylation at two internal N6-methyladenosine sites caused by GAC to GAU mutations.

作者信息

Kane S E, Beemon K

出版信息

J Biol Chem. 1987 Mar 5;262(7):3422-7.

PMID:3029112
Abstract

We previously have mapped N6-methyladenosine (m6A) sites within the genomic RNA of Rous sarcoma virus (RSV). The results of that study and of experiments using inhibitors of methylation suggest that m6A might be involved in mRNA processing events. We describe an approach for directly analyzing the function of m6A in RNA and for studying the sequence specificity of the m6A methylase. Two sites of methylation in RSV (nucleotides 7414 and 7424) were altered by oligonucleotide-directed mutagenesis. The highly conserved GAC consensus sequence at those sites was changed to GAU. The new sequences were no longer methylated in the RSV genomic RNA; the GAC sequence was required for efficient base modification at those two adenosines. The altered m6A pattern did not affect viral RNA processing or the viral life cycle within infected cells.

摘要

我们之前已经绘制了劳氏肉瘤病毒(RSV)基因组RNA中的N6-甲基腺苷(m6A)位点。该研究结果以及使用甲基化抑制剂的实验表明,m6A可能参与mRNA加工事件。我们描述了一种直接分析m6A在RNA中的功能以及研究m6A甲基化酶序列特异性的方法。通过寡核苷酸定向诱变改变了RSV中的两个甲基化位点(核苷酸7414和7424)。这些位点高度保守的GAC共有序列被改为GAU。新序列在RSV基因组RNA中不再被甲基化;GAC序列是这两个腺苷高效碱基修饰所必需的。改变后的m6A模式不影响病毒RNA加工或感染细胞内的病毒生命周期。

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