Lacks S A, Greenberg B, Sabelnikov A G
Brookhaven National Laboratory, Upton, NY 11973, USA.
Gene. 1995 May 19;157(1-2):209-12. doi: 10.1016/0378-1119(94)00481-7.
Atypical ribosome-binding sites lacking Shine-Dalgarno sequences appear to be used for translation of the DpnM and DpnA DNA methyltransferases of the DpnII restriction system. Preliminary results indicate that the 5'-endpoints of DpnII system mRNAs result from degradation of the original transcript. These tentative findings serve as the basis for a possible regulatory model that would accommodate the DpnII cassette either as a single copy in the chromosome or on a multicopy plasmid.