Specific regulation of mRNA cap methylation by the c-Myc and E2F1 transcription factors

被引:66
|
作者
Cole, M. D. [2 ,3 ]
Cowling, V. H. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Div Cell Biol & Immunol, Dundee DD1 5EH, Scotland
[2] Dartmouth Med Sch, Dept Pharmacol, Lebanon, NH USA
[3] Dartmouth Med Sch, Dept Genet, Lebanon, NH USA
关键词
E2F1; gene expression; mRNA cap methylation; Myc; translation; CONDITIONAL MUTANTS; POLYMERASE-II; GENES; EXPRESSION; TRANSLATION; BINDING; IDENTIFICATION; ONCOPROTEINS; RECRUITMENT; ACTIVATION;
D O I
10.1038/onc.2008.463
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Methylation of the mRNA 50 guanosine cap is essential for efficient gene expression. The 50 methyl cap binds to eIF4E, which is the first step in the recruitment of mRNA to the 40S ribosomal subunit. To investigate whether mRNA cap methylation is regulated in a gene-specific manner, we established a method to detect the relative level of cap methylation on specific mRNAs. We found that two transcription factors, c-Myc and E2F1, induce cap methylation of their transcriptional target genes, and therefore, c-Myc and E2F1 upregulate gene expression by simultaneously inducing transcription and promoting translation. c-Myc-induced cap methylation is greater than transcriptional induction for the majority of its target genes, indicating that this is a major mechanism by which Myc regulates gene expression.
引用
收藏
页码:1169 / 1175
页数:7
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