The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases

Werner syndrome (WS) is an autosomal recessive genetic disorder that is manifested by genetic instability and premature onset of age-related diseases, including atherosclerosis and cancer. The gene that is mutated in WS cells ( WRN ) has been identified recently. Characterizations of the WRN gene product indicate that WRN encodes both a 3′→5′ DNA helicase, belonging to the Escherichiacoli RecQ helicase family, and a 3′→5′ DNA exonuclease. Studies to define the molecular mechanism of WRN–DNA transactions are currently underway in many laboratories. Preliminary results indicate that WRN functions as a key factor in resolving aberrant DNA structures that arise from DNA metabolic processes such as replication, recombination and/or repair, to preserve the genetic integrity in cells.