Primary Literature
TEXT HERE
- Adamus K, et al. (2021) SAGA and SAGA-like SLIK transcriptional coactivators are structurally and biochemically equivalent. J Biol Chem 296:100671 PMID: 33864814
- Makio T and Wozniak RW (2020) Passive diffusion through nuclear pore complexes regulates levels of the yeast SAGA and SLIK coactivator complexes. J Cell Sci 133(6) PMID: 32051285
- Jiang Y, et al. (2019) Sfp1 links TORC1 and cell growth regulation to the yeast SAGA-complex component Tra1 in response to polyQ proteotoxicity. Traffic 20(4):267-283 PMID: 30740854
- Torok MS, et al. (2019) The Novel ReNu Region of TAF12 Regulates Gcn5 Nucleosomal Acetylation. J Mol Genet (Isleworth) 2(1) PMID: 32832935
- Berg MD, et al. (2018) The Pseudokinase Domain of <i>Saccharomyces cerevisiae</i> Tra1 Is Required for Nuclear Localization and Incorporation into the SAGA and NuA4 Complexes. G3 (Bethesda) 8(6):1943-1957 PMID: 29626083
- Jiang JC, et al. (2016) Identification of the Target of the Retrograde Response that Mediates Replicative Lifespan Extension in Saccharomyces cerevisiae. Genetics 204(2):659-673 PMID: 27474729
- Kamata K, et al. (2016) Four domains of Ada1 form a heterochromatin boundary through different mechanisms. Genes Cells 21(10):1125-1136 PMID: 27647735
- McClendon TB, et al. (2016) Promotion of Homologous Recombination by SWS-1 in Complex with RAD-51 Paralogs in Caenorhabditis elegans. Genetics 203(1):133-45 PMID: 26936927
- Petty EL, et al. (2016) Promotion of Cell Viability and Histone Gene Expression by the Acetyltransferase Gcn5 and the Protein Phosphatase PP2A in Saccharomyces cerevisiae. Genetics 203(4):1693-707 PMID: 27317677
- Kamata K, et al. (2014) The N-terminus and Tudor domains of Sgf29 are important for its heterochromatin boundary formation function. J Biochem 155(3):159-71 PMID: 24307402
- McCormick MA, et al. (2014) The SAGA histone deubiquitinase module controls yeast replicative lifespan via Sir2 interaction. Cell Rep 8(2):477-86 PMID: 25043177
- Kamata K, et al. (2013) C-terminus of the Sgf73 subunit of SAGA and SLIK is important for retention in the larger complex and for heterochromatin boundary function. Genes Cells 18(9):823-37 PMID: 23819448
- Spedale G, et al. (2010) Identification of Pep4p as the protease responsible for formation of the SAGA-related SLIK protein complex. J Biol Chem 285(30):22793-9 PMID: 20498363
- Mischerikow N, et al. (2009) In-depth profiling of post-translational modifications on the related transcription factor complexes TFIID and SAGA. J Proteome Res 8(11):5020-30 PMID: 19731963
- Soltani J, et al. (2009) Deletion of host histone acetyltransferases and deacetylases strongly affects Agrobacterium-mediated transformation of Saccharomyces cerevisiae. FEMS Microbiol Lett 298(2):228-33 PMID: 19659745
- Yousef AF, et al. (2009) Requirements for E1A dependent transcription in the yeast Saccharomyces cerevisiae. BMC Mol Biol 10:32 PMID: 19374760
- Hoke SM, et al. (2008) Systematic genetic array analysis links the Saccharomyces cerevisiae SAGA/SLIK and NuA4 component Tra1 to multiple cellular processes. BMC Genet 9:46 PMID: 18616809
- Yousef AF, et al. (2008) Coactivator requirements for p53-dependent transcription in the yeast Saccharomyces cerevisiae. Int J Cancer 122(4):942-6 PMID: 17957787
- Daniel JA and Grant PA (2007) Multi-tasking on chromatin with the SAGA coactivator complexes. Mutat Res 618(1-2):135-48 PMID: 17337012
- Hoke SM, et al. (2007) C-terminal processing of yeast Spt7 occurs in the absence of functional SAGA complex. BMC Biochem 8:16 PMID: 17686179
- Jiang L, et al. (2007) Global assessment of combinatorial post-translational modification of core histones in yeast using contemporary mass spectrometry. LYS4 trimethylation correlates with degree of acetylation on the same H3 tail. J Biol Chem 282(38):27923-34 PMID: 17652096
- Roberts GG and Hudson AP (2006) Transcriptome profiling of Saccharomyces cerevisiae during a transition from fermentative to glycerol-based respiratory growth reveals extensive metabolic and structural remodeling. Mol Genet Genomics 276(2):170-86 PMID: 16741729
- Jazwinski SM (2005) The retrograde response links metabolism with stress responses, chromatin-dependent gene activation, and genome stability in yeast aging. Gene 354:22-7 PMID: 15890475
- McMahon SJ, et al. (2005) Polyglutamine-expanded spinocerebellar ataxia-7 protein disrupts normal SAGA and SLIK histone acetyltransferase activity. Proc Natl Acad Sci U S A 102(24):8478-82 PMID: 15932941
- Pray-Grant MG, et al. (2005) Chd1 chromodomain links histone H3 methylation with SAGA- and SLIK-dependent acetylation. Nature 433(7024):434-8 PMID: 15647753
- Daniel JA, et al. (2004) Deubiquitination of histone H2B by a yeast acetyltransferase complex regulates transcription. J Biol Chem 279(3):1867-71 PMID: 14660634
- Kim S, et al. (2004) The histone acetyltransferase GCN5 modulates the retrograde response and genome stability determining yeast longevity. Biogerontology 5(5):305-16 PMID: 15547318
- Lee KK, et al. (2004) Proteomic analysis of chromatin-modifying complexes in Saccharomyces cerevisiae identifies novel subunits. Biochem Soc Trans 32(Pt 6):899-903 PMID: 15506919
- Pray-Grant MG, et al. (2002) The novel SLIK histone acetyltransferase complex functions in the yeast retrograde response pathway. Mol Cell Biol 22(24):8774-86 PMID: 12446794
- Sterner DE, et al. (2002) SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcription. Proc Natl Acad Sci U S A 99(18):11622-7 PMID: 12186975
- Wu PY and Winston F (2002) Analysis of Spt7 function in the Saccharomyces cerevisiae SAGA coactivator complex. Mol Cell Biol 22(15):5367-79 PMID: 12101232