Skip to Main content Skip to Navigation
Journal articles

The Werner syndrome protein has separable recombination and survival functions

Abstract : The Werner syndrome (WS) protein WRN is unique in possessing a 3' to 5' exonuclease activity in addition to the 3' to 5' helicase activity characteristic of other RecQ proteins. In order to determine in vivo functions of the WRN catalytic activities and their roles in Werner syndrome pathogenesis, we quantified cell survival and homologous recombination after DNA damage in cells expressing WRN missense-mutant proteins that lacked exonuclease and/or helicase activity. Both WRN biochemical activities were required to generate viable recombinant daughter cells. In contrast, either activity was sufficient to promote cell survival after DNA damage in the absence of recombination. These results indicate that WRN has recombination and survival functions that can be separated by missense mutations. Two implications are that Werner syndrome most likely results from the loss of both activities and their associated functions from patient cells, and that $WRN$ missense mutations or polymorphisms could promote genetic instability and cancer in the general population by selectively interfering with recombination in somatic cells.
Document type :
Journal articles
Complete list of metadata
Contributor : Yannick Saintigny Connect in order to contact the contributor
Submitted on : Wednesday, November 28, 2018 - 2:38:41 PM
Last modification on : Thursday, November 29, 2018 - 1:58:59 PM


DNA repair_Werner.pdf
Publisher files allowed on an open archive





Cristina Swanson, Yannick Saintigny, Mary J. Emond, Raymond J. Monnat Jr.. The Werner syndrome protein has separable recombination and survival functions. DNA Repair, Elsevier, 2004, 3 (5), pp.475 - 482. ⟨10.1016/j.dnarep.2004.01.002⟩. ⟨cea-01938110⟩



Record views


Files downloads