Gene interactions and pathways from curated databases and text-mining

◀ Back to RAD50

PRR4 — RAD50

Text-mined interactions from Literome

Gangavarapu et al., Mol Cell Biol 2006 : In contrast to the role of Rad5 in PRR , however, where its function is coupled with that of Mms2-Ubc13, Rad5 function in TLS would be largely independent of this ubiquitin conjugating enzyme complex
Zhao et al., Mol Cell 2007 : The ubiquitin ( Ub ) -conjugating enzyme Ubc13 is implicated in Rad6/Rad18 dependent postreplication repair ( PRR ) in budding yeast, but its function in vertebrates is not known
Gangavarapu et al., Mol Cell Biol 2007 : In addition, our results suggest a role for the Rad50 and Xrs2 proteins and thereby for the MRX complex in promoting PRR via both the Rad5 and Rad52 pathways
McIntyre et al., Curr Genet 2007 : The same similarity has previously been reported for yeast deficient in Mms2, a protein involved in Rad6 dependent postreplication DNA repair ( PRR )
Pagès et al., Genetics 2008 : In yeast, Rad6-Rad18 dependent lesion bypass involves translesion synthesis ( TLS ) by DNA polymerases eta or zeta or Rad5 dependent postreplication repair ( PRR ) in which error-free replication through the DNA lesion occurs by template switching
Hishida et al., Mol Cell Biol 2010 : Previously it was shown that the loss of RAD6 dependent error-free postreplication repair ( PRR ) results in DNA damage checkpoint mediated G ( 2 ) arrest in cells exposed to chronic low-dose UV radiation ( CLUV ), whereas wild-type and nucleotide excision repair-deficient cells are largely unaffected
Kozhina et al., Genetika 2012 : Genetic studies on a yeast Saccharomyces cerevisiae model showed that the initial stage of postreplication repair ( PRR ) , i.e., initiation of replication through DNA damage, is controlled by Rad6-Rad18 ubiquitin conjugating enzyme complex