Cargando…
Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1
Repair of DNA double-strand breaks (DSBs) by homologous recombination (HR) requires resection of 5′-termini to generate 3′-single-strand DNA tails(1). Key components of this reaction are Exonuclease 1 and the bifunctional endo/exonuclease, Mre11(2-4). Mre11 endonuclease activity is critical when DSB...
Autores principales: | Garcia, Valerie, Phelps, Sarah E. L., Gray, Stephen, Neale, Matthew J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214165/ https://www.ncbi.nlm.nih.gov/pubmed/22002605 http://dx.doi.org/10.1038/nature10515 |
Ejemplares similares
-
Mre11–Rad50–Xrs2 and Sae2 promote 5’ strand resection of DNA double-strand breaks
por: Nicolette, Matthew L., et al.
Publicado: (2010) -
Analysis of MRE11's function in the 5′→3′ processing of DNA double-strand breaks
por: Liao, Shuren, et al.
Publicado: (2012) -
Processing by MRE11 is involved in the sensitivity of subtelomeric regions to DNA double-strand breaks
por: Muraki, Keiko, et al.
Publicado: (2015) -
Mre11-Rad50 oligomerization promotes DNA double-strand break repair
por: Kissling, Vera M., et al.
Publicado: (2022) -
Ctp1-dependent clipping and resection of DNA double-strand breaks by Mre11 endonuclease complex are not genetically separable
por: Jensen, Kristi L., et al.
Publicado: (2016)