SPT16/YGL207W Literature Guide Help

Other names published for SPT16: CDC68, SSF1, YGL207W

SPT16 - Protein-Nucleic Acid Interactions (22)

ReferenceOther Genes Addressed
Mayer A, et al.  (2012) The spt5 C-terminal region recruits yeast 3' RNA cleavage factor I. Mol Cell Biol 32(7):1321-31
Sikorski TW, et al.  (2012) Proteomic analysis demonstrates activator- and chromatin-specific recruitment to promoters. J Biol Chem 287(42):35397-408
Myers CN, et al.  (2011) Mutant Versions of the S. cerevisiae Transcription Elongation Factor Spt16 Define Regions of Spt16 That Functionally Interact with Histone H3. PLoS One 6(6):e20847
Pruneski JA, et al.  (2011) The Paf1 complex represses SER3 transcription in Saccharomyces cerevisiae by facilitating intergenic transcription-dependent nucleosome occupancy of the SER3 promoter. Eukaryot Cell 10(10):1283-94
Han J, et al.  (2010) Ubiquitylation of FACT by the Cullin-E3 ligase Rtt101 connects FACT to DNA replication. Genes Dev 24(14):1485-90
Fillingham J, et al.  (2009) Two-color cell array screen reveals interdependent roles for histone chaperones and a chromatin boundary regulator in histone gene repression. Mol Cell 35(3):340-51
Lloyd A, et al.  (2009) Uncoupling of the patterns of chromatin association of different transcription elongation factors by a histone H3 mutant in Saccharomyces cerevisiae. Eukaryot Cell 8(2):257-60
Pelechano V, et al.  (2009) Regulon-specific control of transcription elongation across the yeast genome. PLoS Genet 5(8):e1000614
Takahata S, et al.  (2009) FACT and Asf1 regulate nucleosome dynamics and coactivator binding at the HO promoter. Mol Cell 34(4):405-15
Biswas D, et al.  (2008) Different genetic functions for the Rpd3(L) and Rpd3(S) complexes suggest competition between NuA4 and Rpd3(S). Mol Cell Biol 28(14):4445-58
Duina AA, et al.  (2007) Evidence that the Localization of the Elongation Factor Spt16 Across Transcribed Genes Is Dependent Upon Histone H3 Integrity in Saccharomyces cerevisiae. Genetics 177(1):101-12
Tardiff DF, et al.  (2007) Protein characterization of Saccharomyces cerevisiae RNA polymerase II after in vivo cross-linking. Proc Natl Acad Sci U S A 104(50):19948-53
Jimeno-Gonzalez S, et al.  (2006) A Gene-Specific Requirement for FACT during Transcription Is Related to the Chromatin Organization of the Transcribed Region. Mol Cell Biol 26(23):8710-8721
Tackett AJ, et al.  (2005) Proteomic and genomic characterization of chromatin complexes at a boundary. J Cell Biol 169(1):35-47
Yang PK, et al.  (2005) Cotranscriptional recruitment of the pseudouridylsynthetase Cbf5p and of the RNA binding protein Naf1p during H/ACA snoRNP assembly. Mol Cell Biol 25(8):3295-304
Mueller CL, et al.  (2004) The Paf1 complex has functions independent of actively transcribing RNA polymerase II. Mol Cell 14(4):447-56
Rhoades AR, et al.  (2004) Structural features of nucleosomes reorganized by yeast FACT and its HMG box component, Nhp6. Mol Cell Biol 24(9):3907-17
Schwabish MA and Struhl K  (2004) Evidence for eviction and rapid deposition of histones upon transcriptional elongation by RNA polymerase II. Mol Cell Biol 24(23):10111-7
Mason PB and Struhl K  (2003) The FACT complex travels with elongating RNA polymerase II and is important for the fidelity of transcriptional initiation in vivo. Mol Cell Biol 23(22):8323-33
Ruone S, et al.  (2003) Multiple Nhp6 molecules are required to recruit Spt16-Pob3 to form yFACT complexes and to reorganize nucleosomes. J Biol Chem 278(46):45288-95
Krogan NJ, et al.  (2002) RNA polymerase II elongation factors of Saccharomyces cerevisiae: a targeted proteomics approach. Mol Cell Biol 22(20):6979-92
Wittmeyer J, et al.  (1999) Spt16 and Pob3 of Saccharomyces cerevisiae form an essential, abundant heterodimer that is nuclear, chromatin-associated, and copurifies with DNA polymerase alpha. Biochemistry 38(28):8961-71