WRN RQC

Ken Kitano and colleagues have co-crystallised the RecQ C-terminal (RQC) domain of human WRN bound to a DNA duplex. In their recent Structure paper, they describe how the RQC domain interacts with a blunt end of the duplex and, surprisingly, unpairs a Watson-Crick base pair in the absence of an ATPase domain. The β wing, an extended hairpin motif characteristic of winged-helix motifs, is used as a “separating knife” to wedge between the first and second base pair. However, the recognition helix, a component of helix-turn-helix motifs embedded within DNA grooves, is excluded from the interaction.

These results present a function of the winged-helix motif central to the helicase reaction, and add further paradigmatic insights on the structural biology of RecQ helicases.

doi:10.1016/j.str.2009.12.011

Structural Basis for DNA Strand Separation by the Unconventional Winged-Helix Domain of RecQ Helicase WRN

by

Ken Kitano,  Sun-Young Kim, and Toshio Hakoshima

Volume 18, Issue 2, 10 February 2010, Pages 177-187

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Filed under ageing, aging, RecQ, structural biology, Werner Syndrome, WRN

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