posted on 2010-11-22, 11:40authored byCsanád Z. Bachrati, Rhona H. Borts, Ian D. Hickson
The Bloom’s syndrome helicase, BLM, is a member of
the highly conserved RecQ family, and possesses
both DNA unwinding and DNA strand annealing
activities. BLM also promotes branch migration of
Holliday junctions. One role for BLM is to act in conjunction
with topoisomerase IIIa to process homologous
recombination (HR) intermediates containing a
double Holliday junction by a process termed dissolution.
However, several lines of evidence suggest
that BLM may also act early in one or more of the
recombination pathways to eliminate illegitimate or
aberrantly paired DNA joint molecules. We have
investigated whether BLM can disrupt DNA displacement
loops (D-loops), which represent the
initial strand invasion step of HR. We show that
mobile D-loops created by the RecA recombinase
are a highly preferred substrate for BLM with the
invading strand being displaced from the duplex.
We have identified structural features of the D-loop
that determine the efficiency with which BLM promotes
D-loop dissociation. We discuss these results
in the context of models for the role of BLM as an
‘anti-recombinase’.
History
Citation
Nucleic Acids Research, 2006, 34(8), pp. 2269-2279.