YKU80/YMR106C Literature Guide Help

Other names published for YKU80: HDF2, YMR106C

YKU80 - Cellular Location (23)

ReferenceOther Genes Addressed
Kalifa L, et al.  (2012) Mitochondrial genome maintenance: roles for nuclear nonhomologous end-joining proteins in Saccharomyces cerevisiae. Genetics 190(3):951-64
Liu IC, et al.  (2012) The histone deacetylase Hos2 forms an Hsp42-dependent cytoplasmic granule in quiescent yeast cells. Mol Biol Cell 23(7):1231-42
Srividya I, et al.  (2012) Yeast transcription termination factor rtt103 functions in DNA damage response. PLoS One 7(2):e31288
Kitada T, et al.  (2011) gammaH2A is a component of yeast heterochromatin required for telomere elongation. Cell Cycle 10(2):293-300
Marvin ME, et al.  (2009) The association of yKu with subtelomeric core X sequences prevents recombination involving telomeric sequences. Genetics 183(2):453-67, 1SI-13SI
Schober H, et al.  (2009) Yeast telomerase and the SUN domain protein Mps3 anchor telomeres and repress subtelomeric recombination. Genes Dev 23(8):928-38
Zhang Y, et al.  (2009) Regulation of repair choice: Cdk1 suppresses recruitment of end joining factors at DNA breaks. DNA Repair (Amst) 8(10):1235-41
Patterson EE and Fox CA  (2008) The Ku Complex in Silencing the Cryptic Mating-Type Loci of Saccharomyces cerevisiae. Genetics 180(2):771-83
Qi Y, et al.  (2008) Finding friends and enemies in an enemies-only network: A graph diffusion kernel for predicting novel genetic interactions and co-complex membership from yeast genetic interactions. Genome Res 18(12):1991-2004
Sabourin M, et al.  (2007) Telomerase and Tel1p preferentially associate with short telomeres in S. cerevisiae. Mol Cell 27(4):550-61
Hiraga S, et al.  (2006) The Ctf18 RFC-like complex positions yeast telomeres but does not specify their replication time. EMBO J 25(7):1505-14
Taddei A, et al.  (2005) Multiple pathways tether telomeres and silent chromatin at the nuclear periphery: functional implications for sir-mediated repression. Novartis Found Symp 264:140-56; discussion 156-65, 227-30
Gartenberg MR, et al.  (2004) Sir-mediated repression can occur independently of chromosomal and subnuclear contexts. Cell 119(7):955-67
Taddei A, et al.  (2004) Separation of silencing from perinuclear anchoring functions in yeast Ku80, Sir4 and Esc1 proteins. EMBO J 23(6):1301-12
Bertuch AA and Lundblad V  (2003) The Ku heterodimer performs separable activities at double-strand breaks and chromosome termini. Mol Cell Biol 23(22):8202-15
Stellwagen AE, et al.  (2003) Ku interacts with telomerase RNA to promote telomere addition at native and broken chromosome ends. Genes Dev 17(19):2384-95
Frank-Vaillant M and Marcand S  (2002) Transient stability of DNA ends allows nonhomologous end joining to precede homologous recombination. Mol Cell 10(5):1189-99
Gravel S and Wellinger RJ  (2002) Maintenance of double-stranded telomeric repeats as the critical determinant for cell viability in yeast cells lacking Ku. Mol Cell Biol 22(7):2182-93
Luo K, et al.  (2002) Rap1-Sir4 binding independent of other Sir, yKu, or histone interactions initiates the assembly of telomeric heterochromatin in yeast. Genes Dev 16(12):1528-39
Martin SG, et al.  (1999) Relocalization of telomeric Ku and SIR proteins in response to DNA strand breaks in yeast. Cell 97(5):621-33
Friedl AA, et al.  (1998) Radiation-induced chromosome aberrations in Saccharomyces cerevisiae: influence of DNA repair pathways. Genetics 148(3):975-88
Shakibai N, et al.  (1996) The Ku-like protein from Saccharomyces cerevisiae is required in vitro for the assembly of a stable multiprotein complex at a eukaryotic origin of replication. Proc Natl Acad Sci U S A 93(21):11569-74
Feldmann H and Winnacker EL  (1993) A putative homologue of the human autoantigen Ku from Saccharomyces cerevisiae. J Biol Chem 268(17):12895-900