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J. Biol. Chem., Vol. 265, Issue 33, 20117-20122, 11, 1990
T Csepany, A Lin, CJ Baldick Jr and K Beemon
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.
Sequence specificity of mRNA N6-adenosine methyltransferase
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.
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