Crystal structure of the Bloom's syndrome helicase indicates a role for the HRDC domain in conformational changes.

Abstract:

:Bloom's syndrome helicase (BLM) is a member of the RecQ family of DNA helicases, which play key roles in the maintenance of genome integrity in all organism groups. We describe crystal structures of the BLM helicase domain in complex with DNA and with an antibody fragment, as well as SAXS and domain association studies in solution. We show an unexpected nucleotide-dependent interaction of the core helicase domain with the conserved, poorly characterized HRDC domain. The BLM-DNA complex shows an unusual base-flipping mechanism with unique positioning of the DNA duplex relative to the helicase core domains. Comparison with other crystal structures of RecQ helicases permits the definition of structural transitions underlying ATP-driven helicase action, and the identification of a nucleotide-regulated tunnel that may play a role in interactions with complex DNA substrates.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Newman JA,Savitsky P,Allerston CK,Bizard AH,Özer Ö,Sarlós K,Liu Y,Pardon E,Steyaert J,Hickson ID,Gileadi O

doi

10.1093/nar/gkv373

subject

Has Abstract

pub_date

2015-05-26 00:00:00

pages

5221-35

issue

10

eissn

0305-1048

issn

1362-4962

pii

gkv373

journal_volume

43

pub_type

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