Cargando…
Human RECQ1 Interacts with Ku70/80 and Modulates DNA End-Joining of Double-Strand Breaks
Genomic instability is a known precursor to cancer and aging. The RecQ helicases are a highly conserved family of DNA-unwinding enzymes that play key roles in maintaining genome stability in all living organisms. Human RecQ homologs include RECQ1, BLM, WRN, RECQ4, and RECQ5β, three of which have bee...
Autores principales: | Parvathaneni, Swetha, Stortchevoi, Alexei, Sommers, Joshua A., Brosh, Robert M., Sharma, Sudha |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641083/ https://www.ncbi.nlm.nih.gov/pubmed/23650516 http://dx.doi.org/10.1371/journal.pone.0062481 |
Ejemplares similares
-
PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks
por: Couto, C. Anne-Marie, et al.
Publicado: (2011) -
The end-joining factor Ku acts in the end-resection of double strand break-free arrested replication forks
por: Teixeira-Silva, Ana, et al.
Publicado: (2017) -
Distinct roles of XRCC4 and Ku80 in non-homologous end-joining of endonuclease- and ionizing radiation-induced DNA double-strand breaks
por: Schulte-Uentrop, Leonie, et al.
Publicado: (2008) -
Ku80 removal from DNA through double strand break–induced ubiquitylation
por: Postow, Lisa, et al.
Publicado: (2008) -
Ku Regulates the Non-Homologous End Joining Pathway Choice of DNA Double-Strand Break Repair in Human Somatic Cells
por: Fattah, Farjana, et al.
Publicado: (2010)