DNA damage response pathway uses histone modification to assemble a double-strand break-specific cohesin domain.
By Elcin Unal, Ayelet Arbel-Eden, U. Sattler, R. Shroff, M. Lichten, J. Haber, D. Koshland. Molecules and Cells, 2004
613 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/43f59bc69b512c7d0edee4fb44c3e1b35098d3da
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Citations in the corpus
- γ-H2AX Dephosphorylation by Protein Phosphatase 2A Facilitates DNA Double-Strand Break Repair (2005, background): “g-H2AX plays an important role in recruiting some, but probably not all (Celeste et al., 2003), proteins to the repair focus and in stabilizing the repair focus to recruit late factors like cohesins ( Unal et al., 2004 ).”
- Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications. (2011, background): “…of chromosome (SMC) proteins, including cohesins, are recruited to chromosomes in response to DSBs in budding yeast, where they facilitate DSB repair by HR by maintaining sister chromatids in close proximity (Strom et al. 2004; Unal et al. 2004, 2007; De Piccoli et al. 2006; Lindroos et al. 2006).”
- Chromatin challenges during DNA replication and repair. (2007, neutral): “The g -H2AX-dependent loading of cohesin (that mediates sister-chromatid cohesion) provides one example of a postrepair feature of the damaged region (Strom et al., 2004; Unal et al., 2004).”