WRN is recruited to damaged telomeres via its RQC domain and tankyrase1-mediated poly-ADP-ribosylation of TRF1

Werner syndrome (WS) is a progeroid-like syndrome caused by WRN gene mutations. WS cells exhibit shorter telomere length compared to normal cells, but it is not fully understood how WRN deficiency leads directly to telomere dysfunction. By generating localized telomere-specific DNA damage in a real-...

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Detalles Bibliográficos
Autores principales: Sun, Luxi, Nakajima, Satoshi, Teng, Yaqun, Chen, Hao, Yang, Lu, Chen, Xiukai, Gao, Boya, Levine, Arthur S., Lan, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Genome Integrity, Repair and Replication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397154/
https://www.ncbi.nlm.nih.gov/pubmed/28158503
http://dx.doi.org/10.1093/nar/gkx065

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