| Q28081868 | (Ubi)quitin' the h2bit: recent insights into the roles of H2B ubiquitylation in DNA replication and transcription |
| Q42936226 | A Bre1-associated protein, large 1 (Lge1), promotes H2B ubiquitylation during the early stages of transcription elongation |
| Q27670664 | A Role for Intersubunit Interactions in Maintaining SAGA Deubiquitinating Module Structure and Activity |
| Q24307408 | A TFTC/STAGA module mediates histone H2A and H2B deubiquitination, coactivates nuclear receptors, and counteracts heterochromatin silencing |
| Q38551630 | A brief histone in time: understanding the combinatorial functions of histone PTMs in the nucleosome context |
| Q34313810 | A deubiquitylating complex required for neosynthesis of a yeast mitochondrial ATP synthase subunit |
| Q36723292 | A genetic and molecular toolbox for analyzing histone ubiquitylation and sumoylation in yeast. |
| Q33691600 | A global census of fission yeast deubiquitinating enzyme localization and interaction networks reveals distinct compartmentalization profiles and overlapping functions in endocytosis and polarity |
| Q24314096 | A high-confidence interaction map identifies SIRT1 as a mediator of acetylation of USP22 and the SAGA coactivator complex |
| Q24337802 | A histone H2A deubiquitinase complex coordinating histone acetylation and H1 dissociation in transcriptional regulation |
| Q80837134 | A mechanism related to the yeast transcriptional regulator Paf1c is required for expression of the Arabidopsis FLC/MAF MADS box gene family |
| Q37829707 | A modified epigenetics toolbox to study histone modifications on the nucleosome core. |
| Q37947760 | A new chapter in the transcription SAGA. |
| Q30448402 | A novel domain in Set2 mediates RNA polymerase II interaction and couples histone H3 K36 methylation with transcript elongation |
| Q33565860 | A novel histone fold domain-containing protein that replaces TAF6 in Drosophila SAGA is required for SAGA-dependent gene expression |
| Q27939024 | A novel role for Sem1 and TREX-2 in transcription involves their impact on recruitment and H2B deubiquitylation activity of SAGA. |
| Q27934274 | A role for H2B ubiquitylation in DNA replication |
| Q62019752 | A role for Mog1 in H2Bub1 and H3K4me3 regulation affecting RNAPII transcription and mRNA export |
| Q36451302 | A targeted in vivo RNAi screen reveals deubiquitinases as new regulators of Notch signaling. |
| Q37994551 | ATAC-king the complexity of SAGA during evolution |
| Q42772802 | ATXN7L3 and ENY2 Coordinate Activity of Multiple H2B Deubiquitinases Important for Cellular Proliferation and Tumor Growth. |
| Q34165906 | Aberrant expression of USP22 is associated with liver metastasis and poor prognosis of colorectal cancer |
| Q50893480 | Activation of gene expression by histone deubiquitinase OTLD1. |
| Q58375318 | Active site alanine mutations convert deubiquitinases into high-affinity ubiquitin-binding proteins |
| Q36065229 | Aggregation of Polyglutamine-expanded Ataxin 7 Protein Specifically Sequesters Ubiquitin-specific Protease 22 and Deteriorates Its Deubiquitinating Function in the Spt-Ada-Gcn5-Acetyltransferase (SAGA) Complex |
| Q37246670 | Alterations of histone modifications by cobalt compounds |
| Q37352446 | Altered histone monoubiquitylation mediated by mutant huntingtin induces transcriptional dysregulation |
| Q64063488 | Architecture of SAGA complex |
| Q36289979 | Ascending the nucleosome face: recognition and function of structured domains in the histone H2A-H2B dimer |
| Q83230336 | Ataxin-7 and Non-stop coordinate SCAR protein levels, subcellular localization, and actin cytoskeleton organization |
| Q46722207 | Atg19p ubiquitination and the cytoplasm to vacuole trafficking pathway in yeast |
| Q57246269 | BAP1 links metabolic regulation of ferroptosis to tumour suppression |
| Q38122765 | Balancing chromatin remodeling and histone modifications in transcription |
| Q36752292 | Biology of polycomb and trithorax group proteins |
| Q89531833 | Bridging non-overlapping reads illuminates high-order epistasis between distal protein sites in a GPCR |
| Q44778228 | C-terminus of the Sgf73 subunit of SAGA and SLIK is important for retention in the larger complex and for heterochromatin boundary function. |
| Q96136649 | CRISPR screen in regulatory T cells reveals modulators of Foxp3 |
| Q24318345 | Calcium/calmodulin regulates ubiquitination of the ubiquitin-specific protease TRE17/USP6 |
| Q44683549 | Carbohydrates induce mono-ubiquitination of H2B in yeast |
| Q24654957 | Catalysis and substrate selection by histone/protein lysine acetyltransferases |
| Q33984490 | Catalysis-dependent stabilization of Bre1 fine-tunes histone H2B ubiquitylation to regulate gene transcription |
| Q48331605 | Centromeric histone H2B monoubiquitination promotes noncoding transcription and chromatin integrity |
| Q36416226 | Characterization of new Spt3 and TATA-binding protein mutants of Saccharomyces cerevisiae: Spt3 TBP allele-specific interactions and bypass of Spt8. |
| Q27937996 | Chd1 chromodomain links histone H3 methylation with SAGA- and SLIK-dependent acetylation |
| Q37093722 | Chemical Synthesis of Phosphorylated Histone H2A at Tyr57 Reveals Insight into the Inhibition Mode of the SAGA Deubiquitinating Module. |
| Q40343286 | Chemical answers to epigenetic crosstalk. |
| Q46177112 | Chemo-Genetic Interactions Between Histone Modification and the Antiproliferation Drug AICAR Are Conserved in Yeast and Humans |
| Q38987852 | Choose Your Own Adventure: The Role of Histone Modifications in Yeast Cell Fate |
| Q22065678 | Chromatin dynamics at DNA replication, transcription and repair |
| Q37961878 | Chromatin response to DNA double-strand break damage |
| Q33285644 | Chromatin signaling to kinetochores: transregulation of Dam1 methylation by histone H2B ubiquitination |
| Q82282561 | Chromatin-modifying enzymes as therapeutic targets--Part 2 |
| Q27937089 | Cluster analysis of mass spectrometry data reveals a novel component of SAGA |
| Q27932566 | Combinatorial depletion analysis to assemble the network architecture of the SAGA and ADA chromatin remodeling complexes |
| Q26777171 | Composition of the SAGA complex in plants and its role in controlling gene expression in response to abiotic stresses |
| Q35450959 | Conformational flexibility and subunit arrangement of the modular yeast Spt-Ada-Gcn5 acetyltransferase complex |
| Q59070695 | Control of DNA methylation and heterochromatic silencing by histone H2B deubiquitination |
| Q27932002 | Control of transcriptional elongation and cotranscriptional histone modification by the yeast BUR kinase substrate Spt5. |
| Q37275279 | Controlling histone methylation via trans-histone pathways |
| Q41005310 | Cooperation between SAGA and SWI/SNF complexes is required for efficient transcriptional responses regulated by the yeast MAPK Slt2. |
| Q39249006 | Coordinated Actions of MicroRNAs with other Epigenetic Factors Regulate Skeletal Muscle Development and Adaptation |
| Q37777788 | Core histone H2A ubiquitylation and transcriptional regulation |
| Q38973004 | Cotranscriptional histone H2B monoubiquitylation is tightly coupled with RNA polymerase II elongation rate |
| Q36994153 | Covalent modifications of histones during development and disease pathogenesis |
| Q36994157 | Cross-regulation of histone modifications |
| Q36226144 | Cross-talking histones: implications for the regulation of gene expression and DNA repair |
| Q41559771 | Cryo-EM structure of the SAGA and NuA4 coactivator subunit Tra1 at 3.7 angstrom resolution |
| Q35642090 | Ctk complex-mediated regulation of histone methylation by COMPASS. |
| Q58759904 | DET1-mediated degradation of a SAGA-like deubiquitination module controls H2Bub homeostasis |
| Q38336126 | DUBs, the regulation of cell identity and disease |
| Q37069551 | Deciphering histone 2A deubiquitination |
| Q38695071 | Decision for cell fate: deubiquitinating enzymes in cell cycle checkpoint |
| Q35056454 | Decoding the trans-histone crosstalk: methods to analyze H2B ubiquitination, H3 methylation and their regulatory factors. |
| Q37358677 | Decreased histone H2B monoubiquitination in malignant gastric carcinoma |
| Q36678362 | Depletion of the novel p53-target gene carnitine palmitoyltransferase 1C delays tumor growth in the neurofibromatosis type I tumor model |
| Q33195734 | Deubiquitination of histone H2B by a yeast acetyltransferase complex regulates transcription. |
| Q43064198 | Deubiquitylating enzyme UBP64 controls cell fate through stabilization of the transcriptional repressor tramtrack |
| Q28585918 | Deubiquitylation of histone H2A activates transcriptional initiation via trans-histone cross-talk with H3K4 di- and trimethylation |
| Q90575977 | Dissenting degradation: Deubiquitinases in cell cycle and cancer |
| Q34478777 | Distinct regulatory mechanisms of eukaryotic transcriptional activation by SAGA and TFIID |
| Q35203861 | Divergence and selectivity of expression-coupled histone modifications in budding yeasts |
| Q28469221 | Diverse chromatin remodeling genes antagonize the Rb-involved SynMuv pathways in C. elegans |
| Q46495750 | Down-regulation of Pkc1-mediated signaling by the deubiquitinating enzyme Ubp3. |
| Q96950736 | Dynamic modules of the coactivator SAGA in eukaryotic transcription |
| Q47104531 | E3 ubiquitin ligase Bre1 couples sister chromatid cohesion establishment to DNA replication in Saccharomyces cerevisiae. |
| Q28594870 | EPOP Interacts with Elongin BC and USP7 to Modulate the Chromatin Landscape |
| Q27936758 | Effectors of lysine 4 methylation of histone H3 in Saccharomyces cerevisiae are negative regulators of PHO5 and GAL1-10. |
| Q35910114 | Emerging Views on the CTD Code |
| Q39554519 | Enzymatic assays for assessing histone deubiquitylation activity. |
| Q58597542 | Epigenetic mechanisms and implications in tendon inflammation (Review) |
| Q38018086 | Epigenetic mechanisms in gastric cancer |
| Q26740004 | Epigenetic memory: A macrophage perspective |
| Q38002825 | Epigenetic regulation of kallikrein-related peptidases: there is a whole new world out there |
| Q36164758 | Epigenome programming by Polycomb and Trithorax proteins. |
| Q33347428 | Exploiting gene deletion fitness effects in yeast to understand the modular architecture of protein complexes under different growth conditions |
| Q61809019 | FACT and Ubp10 collaborate to modulate H2B deubiquitination and nucleosome dynamics |
| Q35860533 | Feedback Control of Snf1 Protein and Its Phosphorylation Is Necessary for Adaptation to Environmental Stress |
| Q26781153 | Fine-tuning the ubiquitin code at DNA double-strand breaks: deubiquitinating enzymes at work |
| Q42551223 | Flexibility in crosstalk between H2B ubiquitination and H3 methylation in vivo |
| Q35577991 | Flickin' the ubiquitin switch: the role of H2B ubiquitylation in development |
| Q26781247 | Functional Role of G9a Histone Methyltransferase in Cancer |
| Q36742165 | Functional analysis of Bre1p, an E3 ligase for histone H2B ubiquitylation, in regulation of RNA polymerase II association with active genes and transcription in vivo |
| Q42685039 | Functional analysis of H2B-Lys-123 ubiquitination in regulation of H3-Lys-4 methylation and recruitment of RNA polymerase II at the coding sequences of several active genes in vivo |
| Q37468898 | Functional connection between histone acetyltransferase Gcn5p and methyltransferase Hmt1p |
| Q26744570 | Functions of Ubiquitin and SUMO in DNA Replication and Replication Stress |
| Q33493740 | Gcn5 and SAGA regulate shelterin protein turnover and telomere maintenance. |
| Q42065419 | Gcn5 facilitates Pol II progression, rather than recruitment to nucleosome-depleted stress promoters, in Schizosaccharomyces pombe. |
| Q35917883 | Gcn5p-dependent acetylation induces degradation of the meiotic transcriptional repressor Ume6p |
| Q36994161 | Gene regulation through nuclear organization. |
| Q36076885 | Genetic evidence links the ASTRA protein chaperone component Tti2 to the SAGA transcription factor Tra1. |
| Q35124229 | Genetic interactions between POB3 and the acetylation of newly synthesized histones |
| Q39196606 | Genome-wide function of H2B ubiquitylation in promoter and genic regions |
| Q35681247 | Getting into position: the catalytic mechanisms of protein ubiquitylation |
| Q38324759 | Global loss of Set1-mediated H3 Lys4 trimethylation is associated with silencing defects in Saccharomyces cerevisiae |
| Q35294605 | H2B mono-ubiquitylation facilitates fork stalling and recovery during replication stress by coordinating Rad53 activation and chromatin assembly |
| Q36021719 | H2B monoubiquitylation is a 5'-enriched active transcription mark and correlates with exon-intron structure in human cells |
| Q27939759 | H2B ubiquitin protease Ubp8 and Sgf11 constitute a discrete functional module within the Saccharomyces cerevisiae SAGA complex. |
| Q34107829 | H2B ubiquitylation is part of chromatin architecture that marks exon-intron structure in budding yeast. |
| Q92686725 | Histone 2B monoubiquitination complex integrates transcript elongation with RNA processing at circadian clock and flowering regulators |
| Q24309403 | Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB |
| Q24642681 | Histone H2A monoubiquitination represses transcription by inhibiting RNA polymerase II transcriptional elongation |
| Q33963926 | Histone H2B C-terminal helix mediates trans-histone H3K4 methylation independent of H2B ubiquitination. |
| Q53440183 | Histone H2B Monoubiquitination Mediated by HISTONE MONOUBIQUITINATION1 and HISTONE MONOUBIQUITINATION2 Is Involved in Anther Development by Regulating Tapetum Degradation-Related Genes in Rice. |
| Q83012234 | Histone H2B deubiquitination is required for transcriptional activation of FLOWERING LOCUS C and for proper control of flowering in Arabidopsis |
| Q34350965 | Histone H2B monoubiquitination facilitates the rapid modulation of gene expression during Arabidopsis photomorphogenesis |
| Q33346128 | Histone H2B monoubiquitination in the chromatin of FLOWERING LOCUS C regulates flowering time in Arabidopsis |
| Q26825542 | Histone H2B monoubiquitination: roles to play in human malignancy |
| Q35592200 | Histone H2B ubiquitination and beyond: Regulation of nucleosome stability, chromatin dynamics and the trans-histone H3 methylation |
| Q41984790 | Histone H2B ubiquitination promotes the function of the anaphase-promoting complex/cyclosome in Schizosaccharomyces pombe |
| Q37361776 | Histone H2B ubiquitination: the cancer connection |
| Q36238608 | Histone H2B ubiquitylation and deubiquitylation in genomic regulation. |
| Q27936299 | Histone H2B ubiquitylation is associated with elongating RNA polymerase II |
| Q37454264 | Histone H2B ubiquitylation is not required for histone H3 methylation at lysine 4 in tetrahymena |
| Q36896407 | Histone H2B ubiquitylation represses gametogenesis by opposing RSC-dependent chromatin remodeling at the ste11 master regulator locus. |
| Q37309152 | Histone H2BK123 monoubiquitination is the critical determinant for H3K4 and H3K79 trimethylation by COMPASS and Dot1. |
| Q42229711 | Histone H3 K4 demethylation during activation and attenuation of GAL1 transcription in Saccharomyces cerevisiae. |
| Q39891491 | Histone H3 Ser10 phosphorylation-independent function of Snf1 and Reg1 proteins rescues a gcn5- mutant in HIS3 expression |
| Q33930752 | Histone H3 phosphorylation can promote TBP recruitment through distinct promoter-specific mechanisms |
| Q30433574 | Histone acetylation, acetyltransferases, and ataxia--alteration of histone acetylation and chromatin dynamics is implicated in the pathogenesis of polyglutamine-expansion disorders |
| Q29620006 | Histone acetyltransferase complexes: one size doesn't fit all |
| Q36001847 | Histone deacetylase inhibitors: clinical implications for hematological malignancies |
| Q37705706 | Histone modifications as regulators of life and death in Saccharomyces cerevisiae |
| Q37087015 | Histone modifications: Now summoning sumoylation |
| Q33761580 | Histone modifying enzymes: structures, mechanisms, and specificities |
| Q36078818 | Histone monoubiquitylation position determines specificity and direction of enzymatic cross-talk with histone methyltransferases Dot1L and PRC2. |
| Q24545952 | Histone sumoylation is a negative regulator in Saccharomyces cerevisiae and shows dynamic interplay with positive-acting histone modifications |
| Q35971184 | Histone ubiquitination and deubiquitination in transcription, DNA damage response, and cancer |
| Q28081194 | Histone ubiquitylation and its roles in transcription and DNA damage response |
| Q43205547 | How epigenetics integrates nuclear functions. Workshop on epigenetics and chromatin: transcriptional regulation and beyond |
| Q37514183 | How eukaryotic genes are transcribed |
| Q45018971 | Human TREX2 components PCID2 and centrin 2, but not ENY2, have distinct functions in protein export and co-localize to the centrosome |
| Q24299488 | Human USP3 is a chromatin modifier required for S phase progression and genome stability |
| Q89503067 | Hydrazide Mimics for Protein Lysine Acylation To Assess Nucleosome Dynamics and Deubiquitinase Action |
| Q42096517 | Identification of Pep4p as the protease responsible for formation of the SAGA-related SLIK protein complex |
| Q36119924 | Identification of chromatin-associated regulators of MSL complex targeting in Drosophila dosage compensation |
| Q37737546 | Inducible gene expression: diverse regulatory mechanisms |
| Q34671609 | Innate and adaptive factors regulating human immunodeficiency virus type 1 genomic activation. |
| Q37553936 | Insights into SAGA function during gene expression |
| Q36323434 | Interaction of the Jhd2 Histone H3 Lys-4 Demethylase with Chromatin Is Controlled by Histone H2A Surfaces and Restricted by H2B Ubiquitination |
| Q37797693 | Interplay Between Different Epigenetic Modifications and Mechanisms |
| Q35476430 | Invadolysin acts genetically via the SAGA complex to modulate chromosome structure. |
| Q35091097 | Involvement of KDM1C histone demethylase-OTLD1 otubain-like histone deubiquitinase complexes in plant gene repression |
| Q89126426 | Light and temperature shape nuclear architecture and gene expression |
| Q37418113 | Light behind the curtain: photoregulation of nuclear architecture and chromatin dynamics in plants |
| Q41888822 | Light-induced nuclear export reveals rapid dynamics of epigenetic modifications |
| Q91890923 | LncRNA ODIR1 inhibits osteogenic differentiation of hUC-MSCs through the FBXO25/H2BK120ub/H3K4me3/OSX axis |
| Q33837026 | Mapping global histone methylation patterns in the coding regions of human genes |
| Q36580193 | Mapping histone modifications by nucleosome immunoprecipitation |
| Q24307834 | Metabolism, cytoskeleton and cellular signalling in the grip of protein Nepsilon - and O-acetylation |
| Q43122609 | Methylation of H3 K4 and K79 is not strictly dependent on H2B K123 ubiquitylation |
| Q40001798 | Monoubiquitinated H2B is associated with the transcribed region of highly expressed genes in human cells |
| Q24297025 | Monoubiquitination of human histone H2B: the factors involved and their roles in HOX gene regulation |
| Q30443104 | Multi-tasking on chromatin with the SAGA coactivator complexes |
| Q42045741 | Multiple faces of the SAGA complex |
| Q27931794 | Multiple roles for the Ess1 prolyl isomerase in the RNA polymerase II transcription cycle |
| Q27930623 | Mutational analysis of the C-terminal FATC domain of Saccharomyces cerevisiae Tra1. |
| Q27933670 | Mutational uncoupling of the role of Sus1 in nuclear pore complex targeting of an mRNA export complex and histone H2B deubiquitination |
| Q40251253 | Ni(II) affects ubiquitination of core histones H2B and H2A. |
| Q90185691 | Nipped-A regulates the Drosophila circadian clock via histone deubiquitination |
| Q33963762 | Novel trans-tail regulation of H2B ubiquitylation and H3K4 methylation by the N terminus of histone H2A. |
| Q42114752 | Nucleosomal H2B ubiquitylation with purified factors |
| Q46268719 | On your MARKS, get SET, METHYLATE! |
| Q42598151 | Paf1 restricts Gcn4 occupancy and antisense transcription at the ARG1 promoter |
| Q30445180 | Phosphorylation of histone H4 Ser1 regulates sporulation in yeast and is conserved in fly and mouse spermatogenesis. |
| Q89621389 | Plant Chromatin Catches the Sun |
| Q36854975 | Polyubiquitylation of histone H2B. |
| Q42609408 | Post-transcription initiation function of the ubiquitous SAGA complex in tissue-specific gene activation |
| Q26852536 | Post-translational modifications of histones that influence nucleosome dynamics |
| Q33370815 | Probing nucleosome function: a highly versatile library of synthetic histone H3 and H4 mutants |
| Q39673659 | Promotion of Cell Viability and Histone Gene Expression by the Acetyltransferase Gcn5 and the Protein Phosphatase PP2A in Saccharomyces cerevisiae. |
| Q37249177 | Protein modifications in transcription elongation |
| Q36554464 | Protein monoubiquitylation: targets and diverse functions |
| Q36199691 | Proteomic analysis revealed nitrogen-mediated metabolic, developmental, and hormonal regulation of maize (Zea mays L.) ear growth |
| Q30375585 | Quantitative proteomic analysis of histone modifications |
| Q40406028 | Quantitative sequential chromatin immunoprecipitation, a method for analyzing co-occupancy of proteins at genomic regions in vivo |
| Q36029959 | RNF20 and USP44 regulate stem cell differentiation by modulating H2B monoubiquitylation |
| Q34995984 | RNF20 inhibits TFIIS-facilitated transcriptional elongation to suppress pro-oncogenic gene expression |
| Q37914341 | RNF20-RNF40: A ubiquitin-driven link between gene expression and the DNA damage response. |
| Q26799882 | RNF20-SNF2H Pathway of Chromatin Relaxation in DNA Double-Strand Break Repair |
| Q27930655 | Rad6 plays a role in transcriptional activation through ubiquitylation of histone H2B. |
| Q27932934 | Rad6-Bre1-mediated histone H2B ubiquitylation modulates the formation of double-strand breaks during meiosis |
| Q41999449 | Recognition of trimethylated histone H3 lysine 4 facilitates the recruitment of transcription postinitiation factors and pre-mRNA splicing |
| Q39030776 | Recognition of ubiquitinated nucleosomes. |
| Q28270922 | Recombination-activating gene proteins: more regulation, please |
| Q24645701 | Regulation and cellular roles of ubiquitin-specific deubiquitinating enzymes |
| Q39705425 | Regulation of an intergenic transcript controls adjacent gene transcription in Saccharomyces cerevisiae. |
| Q24793292 | Regulation of androgen receptor and histone deacetylase 1 by Mdm2-mediated ubiquitylation |
| Q24296401 | Regulation of cell cycle progression and gene expression by H2A deubiquitination |
| Q34606198 | Regulation of histone H2A and H2B deubiquitination and Xenopus development by USP12 and USP46. |
| Q42070422 | Regulation of mitochondrial morphology by USP30, a deubiquitinating enzyme present in the mitochondrial outer membrane |
| Q38855269 | Regulation of pluripotency and differentiation by deubiquitinating enzymes |
| Q33431467 | Requirements for E1A dependent transcription in the yeast Saccharomyces cerevisiae |
| Q35105237 | Rescue of DNA damage-stalled RNA Pol II: histone H2B in action |
| Q48014985 | Retracted: Histone H2B ubquitination regulates retinoic acid signaling through the cooperation of ASXL1 and BAP1. |
| Q26773800 | Role of Deubiquitinating Enzymes in DNA Repair |
| Q41493041 | Role of Doa1 in the Saccharomyces cerevisiae DNA damage response |
| Q24305090 | Role of histone H2A ubiquitination in Polycomb silencing |
| Q34115523 | Rrd1p, an RNA polymerase II-specific prolyl isomerase and activator of phosphoprotein phosphatase, promotes transcription independently of rapamycin response |
| Q27929974 | Rtf1 is a multifunctional component of the Paf1 complex that regulates gene expression by directing cotranscriptional histone modification |
| Q36574522 | SAGA DUB-Ubp8 Deubiquitylates Centromeric Histone Variant Cse4. |
| Q92531896 | SAGA DUBm-mediated surveillance regulates prompt export of stress-inducible transcripts for proteostasis |
| Q47790116 | SAGA Is a General Cofactor for RNA Polymerase II Transcription. |
| Q41620842 | SAGA complex components and acetate repression in Aspergillus nidulans |
| Q42552805 | SAGA function in tissue-specific gene expression |
| Q27934681 | SAGA-associated Sgf73p facilitates formation of the preinitiation complex assembly at the promoters either in a HAT-dependent or independent manner in vivo |
| Q41953553 | SAGA-mediated H2B deubiquitination controls the development of neuronal connectivity in the Drosophila visual system |
| Q53556000 | SIN-fully silent: HDAC complexes in fission yeast. |
| Q36421035 | STAGA recruits Mediator to the MYC oncoprotein to stimulate transcription and cell proliferation |
| Q42289702 | Sas3 and Ada2(Gcn5)-dependent histone H3 acetylation is required for transcription elongation at the de-repressed FLO1 gene. |
| Q21129202 | Seed dormancy and germination-emerging mechanisms and new hypotheses |
| Q61207709 | Separation of a functional deubiquitylating module from the SAGA complex by the proteasome regulatory particle |
| Q27930044 | Sgf29p facilitates the recruitment of TATA box binding protein but does not alter SAGA's global structural integrity in vivo |
| Q36073403 | Shaping the landscape: mechanistic consequences of ubiquitin modification of chromatin. |
| Q47721313 | Sharing the SAGA. |
| Q28511362 | Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis |
| Q27026725 | Single molecule and single cell epigenomics. |
| Q36079423 | Small region of Rtf1 protein can substitute for complete Paf1 complex in facilitating global histone H2B ubiquitylation in yeast |
| Q33628559 | Snf1p regulates Gcn5p transcriptional activity by antagonizing Spt3p |
| Q35559126 | Splitting the task: Ubp8 and Ubp10 deubiquitinate different cellular pools of H2BK123. |
| Q27661081 | Structural Basis for Assembly and Activation of the Heterotetrameric SAGA Histone H2B Deubiquitinase Module |
| Q27660560 | Structural Insights into the Assembly and Function of the SAGA Deubiquitinating Module |
| Q42196568 | Structural and biochemical analyses of monoubiquitinated human histones H2B and H4. |
| Q36892380 | Structural basis for histone H2B deubiquitination by the SAGA DUB module. |
| Q27646584 | Structural basis for the interaction between yeast Spt-Ada-Gcn5 acetyltransferase (SAGA) complex components Sgf11 and Sus1. |
| Q45889376 | Structure of the transcription activator target Tra1 within the chromatin modifying complex SAGA. |
| Q92860926 | Structure of the transcription coactivator SAGA |
| Q36942429 | Sus1 is recruited to coding regions and functions during transcription elongation in association with SAGA and TREX2. |
| Q38051409 | Sus1/ENY2: a multitasking protein in eukaryotic gene expression |
| Q33940735 | Sus1p facilitates pre-initiation complex formation at the SAGA-regulated genes independently of histone H2B de-ubiquitylation |
| Q24545962 | TFIID and Spt-Ada-Gcn5-acetyltransferase functions probed by genome-wide synthetic genetic array analysis using a Saccharomyces cerevisiae taf9-ts allele |
| Q53201323 | Targeting the epigenome for treatment of cancer. |
| Q41841500 | Temperature-sensitive post-translational regulation of plant omega-3 fatty-acid desaturases is mediated by the endoplasmic reticulum-associated degradation pathway |
| Q37592212 | Temporal and spatial regulation of V(D)J recombination: interactions of extrinsic factors with the RAG complex |
| Q28742012 | The C-terminus of histone H2B is involved in chromatin compaction specifically at telomeres, independently of its monoubiquitylation at lysine 123 |
| Q26765873 | The Importance of Ubiquitination and Deubiquitination in Cellular Reprogramming |
| Q35104140 | The Ino80 complex prevents invasion of euchromatin into silent chromatin |
| Q27935220 | The N-terminus and Tudor domains of Sgf29 are important for its heterochromatin boundary formation function |
| Q35737433 | The Nucleosome Acidic Patch Regulates the H2B K123 Monoubiquitylation Cascade and Transcription Elongation in Saccharomyces cerevisiae |
| Q27935853 | The Paf1 complex promotes displacement of histones upon rapid induction of transcription by RNA polymerase II |
| Q42782209 | The Paf1 complex represses ARG1 transcription in Saccharomyces cerevisiae by promoting histone modifications |
| Q38627903 | The Paf1 complex represses SER3 transcription in Saccharomyces cerevisiae by facilitating intergenic transcription-dependent nucleosome occupancy of the SER3 promoter |
| Q52329552 | The Pseudokinase Domain of Saccharomyces cerevisiae Tra1 Is Required for Nuclear Localization and Incorporation into the SAGA and NuA4 Complexes. |
| Q35811839 | The Roles of the Paf1 Complex and Associated Histone Modifications in Regulating Gene Expression |
| Q36995417 | The S. pombe SAGA complex controls the switch from proliferation to sexual differentiation through the opposing roles of its subunits Gcn5 and Spt8. |
| Q36955793 | The SAGA Deubiquitination Module Promotes DNA Repair and Class Switch Recombination through ATM and DNAPK-Mediated γH2AX Formation. |
| Q34235677 | The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription. |
| Q30438554 | The SAGA continues: expanding the cellular role of a transcriptional co-activator complex |
| Q41521346 | The SAGA histone acetyltransferase complex regulates leucine uptake through the Agp3 permease in fission yeast |
| Q34824438 | The SAGA histone deubiquitinase module controls yeast replicative lifespan via Sir2 interaction. |
| Q51415405 | The SAGA/TREX-2 subunit Sus1 binds widely to transcribed genes and affects mRNA turnover globally. |
| Q39761741 | The Spliceosomal Protein SF3B5 is a Novel Component of Drosophila SAGA that Functions in Gene Expression Independent of Splicing |
| Q34769706 | The Spt-Ada-Gcn5 Acetyltransferase (SAGA) complex in Aspergillus nidulans |
| Q35910444 | The Transition of Poised RNA Polymerase II to an Actively Elongating State Is a "Complex" Affair |
| Q24337279 | The U4/U6 recycling factor SART3 has histone chaperone activity and associates with USP15 to regulate H2B deubiquitination |
| Q27932371 | The Ubp15 deubiquitinase promotes timely entry into S phase in Saccharomyces cerevisiae |
| Q48081222 | The absence of histone H2B monoubiquitination in the Arabidopsis hub1 (rdo4) mutant reveals a role for chromatin remodeling in seed dormancy |
| Q47069099 | The bromodomain protein LEX-1 acts with TAM-1 to modulate gene expression in C. elegans |
| Q38352748 | The cap binding complex influences H2B ubiquitination by facilitating splicing of the SUS1 pre-mRNA |
| Q34566036 | The chromatin signaling pathway: diverse mechanisms of recruitment of histone-modifying enzymes and varied biological outcomes |
| Q28131748 | The complex language of chromatin regulation during transcription |
| Q27932453 | The deubiquitylation activity of Ubp8 is dependent upon Sgf11 and its association with the SAGA complex |
| Q29614523 | The diverse functions of histone lysine methylation |
| Q35666251 | The diverse superfamily of lysine acetyltransferases and their roles in leukemia and other diseases |
| Q38008101 | The enigmatic role of H2Bub1 in cancer |
| Q39140357 | The epigenetic modifier ubiquitin-specific protease 22 (USP22) regulates embryonic stem cell differentiation via transcriptional repression of sex-determining region Y-box 2 (SOX2). |
| Q37186709 | The epigenetics of adult (somatic) stem cells |
| Q24318500 | The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression |
| Q24298372 | The human homolog of yeast BRE1 functions as a transcriptional coactivator through direct activator interactions |
| Q49723158 | The interplay of histone H2B ubiquitination with budding and fission yeast heterochromatin. |
| Q58616112 | The kinetochore module Okp1/Ame1 is a reader for N-terminal modifications on the centromeric histone Cse4 |
| Q27940177 | The mRNA export factor Sus1 is involved in Spt/Ada/Gcn5 acetyltransferase-mediated H2B deubiquitinylation through its interaction with Ubp8 and Sgf11. |
| Q37862125 | The multifaceted roles of USP7: new therapeutic opportunities |
| Q36579378 | The multiple faces of Set1. |
| Q92937229 | The nucleosome acidic patch directly interacts with subunits of the Paf1 and FACT complexes and controls chromatin architecture in vivo |
| Q28240753 | The nucleosome: from genomic organization to genomic regulation |
| Q24307439 | The putative cancer stem cell marker USP22 is a subunit of the human SAGA complex required for activated transcription and cell-cycle progression |
| Q35147589 | The role of Candida albicans SPT20 in filamentation, biofilm formation and pathogenesis |
| Q34564968 | The role of deubiquitinating enzymes in chromatin regulation. |
| Q80188867 | The role of histone ubiquitylation and deubiquitylation in gene expression as determined by the analysis of an HTB1(K123R) Saccharomyces cerevisiae strain |
| Q24338865 | The structural plasticity of SCA7 domains defines their differential nucleosome-binding properties |
| Q34199540 | The tightly controlled deubiquitination activity of the human SAGA complex differentially modifies distinct gene regulatory elements |
| Q50335555 | The trithorax-group protein Lid is a histone H3 trimethyl-Lys4 demethylase |
| Q33600336 | The ubiquitin-conjugating enzyme HR6B is required for maintenance of X chromosome silencing in mouse spermatocytes and spermatids. |
| Q36268060 | The ubiquitin-proteasome system of Saccharomyces cerevisiae |
| Q27934454 | The ubiquitin-selective chaperone Cdc48/p97 associates with Ubx3 to modulate monoubiquitylation of histone H2B. |
| Q49601869 | The ubiquitin-specific protease USP36 is a conserved histone H2B deubiquitinase |
| Q27937658 | The yeast SR-like protein Npl3 links chromatin modification to mRNA processing |
| Q27937396 | Tight cooperation between Mot1p and NC2β in regulating genome-wide transcription, repression of transcription following heat shock induction and genetic interaction with SAGA |
| Q24314891 | Trabid, a new positive regulator of Wnt-induced transcription with preference for binding and cleaving K63-linked ubiquitin chains |
| Q57970965 | Transcription and mRNA export machineries SAGA and TREX-2 maintain monoubiquitinated H2B balance required for DNA repair |
| Q38043829 | Transcription-associated histone modifications and cryptic transcription |
| Q42133855 | Transcriptional elongation and mRNA export are coregulated processes. |
| Q36040816 | Transcriptome Profiling Identifies Multiplexin as a Target of SAGA Deubiquitinase Activity in Glia Required for Precise Axon Guidance During Drosophila Visual Development |
| Q36830110 | Treatment of Plasmodium chabaudi Parasites with Curcumin in Combination with Antimalarial Drugs: Drug Interactions and Implications on the Ubiquitin/Proteasome System |
| Q92490294 | Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA |
| Q80049453 | Two tales of chromatin remodeling converge on HUB1 |
| Q38953607 | Tyrosine phosphorylation of histone H2A by CK2 regulates transcriptional elongation |
| Q42074560 | UBIQUITIN-SPECIFIC PROTEASE 26 is required for seed development and the repression of PHERES1 in Arabidopsis. |
| Q88909318 | USP22 deficiency leads to myeloid leukemia upon oncogenic Kras activation through a PU.1-dependent mechanism |
| Q34374287 | USP22 is useful as a novel molecular marker for predicting disease progression and patient prognosis of oral squamous cell carcinoma |
| Q24311562 | USP22, an hSAGA subunit and potential cancer stem cell marker, reverses the polycomb-catalyzed ubiquitylation of histone H2A |
| Q38729273 | USP44 Is an Integral Component of N-CoR that Contributes to Gene Repression by Deubiquitinating Histone H2B. |
| Q24297433 | USP49 deubiquitinates histone H2B and regulates cotranscriptional pre-mRNA splicing |
| Q34144605 | UV damage-induced RNA polymerase II stalling stimulates H2B deubiquitylation |
| Q47359149 | Ubiquitin Specific Peptidase 22 Regulates Histone H2B Mono-Ubiquitination and Exhibits Both Oncogenic and Tumor Suppressor Roles in Cancer |
| Q38702950 | Ubiquitin crosstalk connecting cellular processes |
| Q26750743 | Ubiquitin-specific peptidase 22 functions and its involvement in disease |
| Q38924763 | Ubiquitin-specific protease 22 (USP22) positively regulates RCAN1 protein levels through RCAN1 de-ubiquitination |
| Q37679191 | Ubiquitination regulates the morphogenesis and function of sperm organelles |
| Q33884138 | Ubp10/Dot4p regulates the persistence of ubiquitinated histone H2B: distinct roles in telomeric silencing and general chromatin |
| Q35139409 | Ubp8 and SAGA regulate Snf1 AMP kinase activity. |
| Q42222766 | Ubp8p, a histone deubiquitinase whose association with SAGA is mediated by Sgf11p, differentially regulates lysine 4 methylation of histone H3 in vivo |
| Q27931833 | Uncovering the role of Sgf73 in maintaining SAGA deubiquitinating module structure and activity |
| Q43088502 | Using glycinylation, a chemical derivatization technique, for the quantitation of ubiquitinated proteins |
| Q24293427 | WAC, a functional partner of RNF20/40, regulates histone H2B ubiquitination and gene transcription |
| Q49911687 | Whole-Genome Sequencing of Suppressor DNA Mixtures Identifies Pathways That Compensate for Chromosome Segregation Defects in Schizosaccharomyces pombe. |
| Q26742134 | Writers, Readers, and Erasers of Histone Ubiquitylation in DNA Double-Strand Break Repair |
| Q27936733 | Yeast Ataxin-7 links histone deubiquitination with gene gating and mRNA export |
| Q27935396 | Yeast Sgf73/Ataxin-7 serves to anchor the deubiquitination module into both SAGA and Slik(SALSA) HAT complexes |
| Q45954525 | dDsk2 regulates H2Bub1 and RNA polymerase II pausing at dHP1c complex target genes. |
| Q35442854 | dRYBP counteracts chromatin-dependent activation and repression of transcription |
| Q47134084 | let-7b and let-7c microRNAs promote histone H2B ubiquitylation and inhibit cell migration by targeting multiple components of the H2B deubiquitylation machinery |