Nucleic Acids Research, Vol 25, Issue 4 7-14, Copyright © 1997 by Oxford University Press
BS Strauss, D Sagher and S Acharya
The role of the proofreading exonuclease in maintaining the stability of
multiply repeated units in DNA was studied inEscherichia coli. Reversion of
plasmids in which thebeta-galactosidasealphacomplementing sequence was
moved +2 out of frame by inserts containing (CA)14, (CA)5, (CA)2or (TA)6or
+1 by creating a run of 8 C was compared inmutSandmutSdnaQstrains.
Proofreading corrects at least half of the frameshift errors for all the
plasmids and at least 99% of the errors in the (CA)2plasmid. The
(CA)2plasmid reverts mostly by +1 frameshifts in the restriction sites
flanking the insert. With the (CA)14, (TA)6, (CA)5and 8C plasmids,
reversion is mainly by loss of a repeat unit. The data support the
hypothesis that thednaQgene product recognizes frameshifts close to the DNA
growing point. Frameshifts distal to the growing point are mainly corrected
by mismatch repair.We speculate that mismatches in mononucleotide repeats
are susceptible to proofreading because they can either migrate to a point
where they are recognized by the exonuclease or, alternatively, because
single nucleotide distortions are more readily detected than dinucleotides.
ARTICLES
Role of proofreading and mismatch repair in maintaining the stability of nucleotide repeats in DNA
Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago , IL 60637, USA
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