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Regulation of the Rhp26ERCC6/CSBchromatin remodeler by a novel conserved leucine latch motif

Authors :
Wang, L
Limbo, O
Fei, J
Chen, L
Kim, B
Luo, J
Chong, J
Conaway, RC
Conaway, JW
Ranish, JA
Kadonaga, JT
Russell, P
Wang, D
Source :
Wang, L; Limbo, O; Fei, J; Chen, L; Kim, B; Luo, J; et al.(2014). Regulation of the Rhp26ERCC6/CSBchromatin remodeler by a novel conserved leucine latch motif. Proceedings of the National Academy of Sciences of the United States of America, 111(52), 18566-18571. doi: 10.1073/pnas.1420227112. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/9fq128n3
Publication Year :
2014
Publisher :
eScholarship, University of California, 2014.

Abstract

© 2014, National Academy of Sciences. All Rights Reserved. CSB/ERCC6 (Cockayne syndrome B protein/excision repair cross-complementation group 6), a member of a subfamily of SWI2/SNF2 (SWItch/sucrose nonfermentable)-related chromatin remodelers, plays crucial roles in gene expression and the maintenance of genome integrity. Here, we report the mechanism of the autoregulation of Rhp26, which is the homolog of CSB/ERCC6 in Schizosaccharomyces pombe. We identified a novel conserved protein motif, termed the "leucine latch," at the N terminus of Rhp26. The leucine latch motif mediates the autoinhibition of the ATPase and chromatin-remodeling activities of Rhp26 via its interaction with the core ATPase domain. Moreover, we found that the C terminus of the protein counteracts this autoinhibition and that both the N- and C-terminal regions of Rhp26 are needed for its proper function in DNA repair in vivo. The presence of the leucine latch motif in organisms ranging from yeast to humans suggests a conserved mechanism for the autoregulation of CSB/ERCC6 despite the otherwise highly divergent nature of the N- and C-terminal regions.

Details

Language :
English
Database :
OpenAIRE
Journal :
Wang, L; Limbo, O; Fei, J; Chen, L; Kim, B; Luo, J; et al.(2014). Regulation of the Rhp26ERCC6/CSBchromatin remodeler by a novel conserved leucine latch motif. Proceedings of the National Academy of Sciences of the United States of America, 111(52), 18566-18571. doi: 10.1073/pnas.1420227112. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/9fq128n3
Accession number :
edsair.od.......325..18fa2476ac094c89d3700c502287812a