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J. Biol. Chem., Vol. 265, Issue 33, 20117-20122, 11, 1990

Sequence specificity of mRNA N6-adenosine methyltransferase

T Csepany, A Lin, CJ Baldick Jr and K Beemon
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.

The sequence specificity of chicken mRNA N6-adenosine methyltransferase has been investigated in vivo. Localization of six new N6- methyladenosine sites on Rous sarcoma virus (RSV) virion RNA has confirmed our extended consensus sequence for methylation: RGACU, where R is usually a G (7/12). We have also observed A (2/12) and U (3/12) at the -2 position (relative to m6A at +1) but never a C. At the +3 position, the U was observed 10/12 times; an A and a C were observed once each in weakly methylated sequences. The extent of methylation varied between the different sites up to a maximum of about 90%. To test the significance of this consensus sequence, it was altered by site-specific mutagenesis, and methylation was assayed after transfection of mutated RSV DNA into chicken embryo fibroblasts. We found that changing the G at -1 or the U at +3 to any other residue inhibited methylation. However, inhibition of methylation at all four of the major sites in the RSV src gene did not detectably alter the steady-state levels of the three viral RNA species or viral infectivity. Additional mutants that inactivated the src protein kinase activity produced less virus and exhibited relatively less src mRNA in infected cells.
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Nucleic Acids ResHome page
M. J. Clancy, M. E. Shambaugh, C. S. Timpte, and J. A. Bokar
Induction of sporulation in Saccharomyces cerevisiae leads to the formation of N6-methyladenosine in mRNA: a potential mechanism for the activity of the IME4 gene
Nucleic Acids Res., October 15, 2002; 30(20): 4509 - 4518.
[Abstract] [Full Text] [PDF]




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