LEO1/YOR123C Literature Guide Help

Other names published for LEO1: YOR123C

LEO1 - Primary Literature (21)

ReferenceOther Genes Addressed
Mosley AL, et al.  (2013) Quantitative Proteomics Demonstrates that the RNA Polymerase II Subunits Rpb4 and Rpb7 Dissociate During Transcription Elongation. Mol Cell Proteomics ()
Tomson BN, et al.  (2013) Effects of the Paf1 Complex and Histone Modifications on snoRNA 3'-End Formation Reveal Broad and Locus-Specific Regulation. Mol Cell Biol 33(1):170-82
Qiu H, et al.  (2012) Pol II CTD kinases Bur1 and Kin28 promote Spt5 CTR-independent recruitment of Paf1 complex. EMBO J 31(16):3494-505
Lenstra TL, et al.  (2011) The specificity and topology of chromatin interaction pathways in yeast. Mol Cell 42(4):536-49
Tatum D, et al.  (2011) Diverse roles of RNA polymerase II-associated factor 1 complex in different subpathways of nucleotide excision repair. J Biol Chem 286(35):30304-13
Tous C, et al.  (2011) A novel assay identifies transcript elongation roles for the Nup84 complex and RNA processing factors. EMBO J 30(10):1953-64
Dermody JL and Buratowski S  (2010) Leo1 subunit of the yeast paf1 complex binds RNA and contributes to complex recruitment. J Biol Chem 285(44):33671-9
Zhang Y, et al.  (2010) The RNA polymerase-associated factor 1 complex (Paf1C) directly increases the elongation rate of RNA polymerase I and is required for efficient regulation of rRNA synthesis. J Biol Chem 285(19):14152-9
Kim J and Roeder RG  (2009) Direct Bre1-Paf1 Complex Interactions and RING Finger-independent Bre1-Rad6 Interactions Mediate Histone H2B Ubiquitylation in Yeast. J Biol Chem 284(31):20582-92
Mozdy AD, et al.  (2008) Multiple yeast genes, including Paf1 complex genes, affect telomere length via telomerase RNA abundance. Mol Cell Biol 28(12):4152-61
Nyswaner KM, et al.  (2008) Chromatin-associated genes protect the yeast genome from ty1 insertional mutagenesis. Genetics 178(1):197-214
Porter SE, et al.  (2005) Separation of the Saccharomyces cerevisiae Paf1 complex from RNA polymerase II results in changes in its subnuclear localization. Eukaryot Cell 4(1):209-20
Aye M, et al.  (2004) Host factors that affect Ty3 retrotransposition in Saccharomyces cerevisiae. Genetics 168(3):1159-76
Mueller CL, et al.  (2004) The Paf1 complex has functions independent of actively transcribing RNA polymerase II. Mol Cell 14(4):447-56
Rondon AG, et al.  (2004) Molecular evidence indicating that the yeast PAF complex is required for transcription elongation. EMBO Rep 5(1):47-53
Krogan NJ, et al.  (2003) The Paf1 complex is required for histone H3 methylation by COMPASS and Dot1p: linking transcriptional elongation to histone methylation. Mol Cell 11(3):721-9
Wood A, et al.  (2003) The Paf1 complex is essential for histone monoubiquitination by the Rad6-Bre1 complex, which signals for histone methylation by COMPASS and Dot1p. J Biol Chem 278(37):34739-42
Betz JL, et al.  (2002) Phenotypic analysis of Paf1/RNA polymerase II complex mutations reveals connections to cell cycle regulation, protein synthesis, and lipid and nucleic acid metabolism. Mol Genet Genomics 268(2):272-85
Mueller CL and Jaehning JA  (2002) Ctr9, Rtf1, and Leo1 are components of the Paf1/RNA polymerase II complex. Mol Cell Biol 22(7):1971-80
Squazzo SL, et al.  (2002) The Paf1 complex physically and functionally associates with transcription elongation factors in vivo. EMBO J 21(7):1764-74
Magdolen V, et al.  (1994) The gene LEO1 on yeast chromosome XV encodes a non-essential, extremely hydrophilic protein. Biochim Biophys Acta 1218(2):205-9