scholarly article | Q13442814 |
P50 | author | Hélène Gaillard | Q57041661 |
Joaquin Arino | Q60503389 | ||
Alfonso Rodríguez-Gil | Q79458013 | ||
Cristina González-Aguilera | Q81720268 | ||
María L García-Rubio | Q43158419 | ||
José L. Revuelta | Q36597850 | ||
Sebastián Chávez | Q37374358 | ||
Andrés Aguilera | Q37382275 | ||
P2093 | author name string | Laia Viladevall | |
Antonio Marín | |||
Javier Botet | |||
Cristina Tous | |||
Maria José Quintero | |||
P2860 | cites work | CCR4, a 3'-5' poly(A) RNA and ssDNA exonuclease, is the catalytic component of the cytoplasmic deadenylase | Q24292432 |
Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome | Q24292732 | ||
Cockayne syndrome group B protein enhances elongation by RNA polymerase II | Q24317053 | ||
DNA damage and replication stress induced transcription of RNR genes is dependent on the Ccr4-Not complex. | Q24815044 | ||
Genome-wide requirements for resistance to functionally distinct DNA-damaging agents | Q24815105 | ||
Roles for Gcn5p and Ada2p in transcription and nucleotide excision repair at the Saccharomyces cerevisiae MET16 gene | Q25256763 | ||
The yeast THO complex and mRNA export factors link RNA metabolism with transcription and genome instability | Q27929526 | ||
Ccr4 contributes to tolerance of replication stress through control of CRT1 mRNA poly(A) tail length | Q27929903 | ||
Evidence that the transcription elongation function of Rpb9 is involved in transcription-coupled DNA repair in Saccharomyces cerevisiae | Q27930103 | ||
Bur1 kinase is required for efficient transcription elongation by RNA polymerase II. | Q27930313 | ||
Molecular evidence for a positive role of Spt4 in transcription elongation | Q27930449 | ||
The yeast Ccr4-Not complex controls ubiquitination of the nascent-associated polypeptide (NAC-EGD) complex | Q27930672 | ||
Characterization of the calcium-mediated response to alkaline stress in Saccharomyces cerevisiae. | Q27930851 | ||
The Paf1 complex is required for histone H3 methylation by COMPASS and Dot1p: linking transcriptional elongation to histone methylation | Q27930884 | ||
Genetic evidence supports a role for the yeast CCR4-NOT complex in transcriptional elongation. | Q27930971 | ||
Cell cycle progression in G1 and S phases is CCR4 dependent following ionizing radiation or replication stress in Saccharomyces cerevisiae | Q27931688 | ||
A new connection of mRNP biogenesis and export with transcription-coupled repair | Q27931906 | ||
Direct interactions between the Paf1 complex and a cleavage and polyadenylation factor are revealed by dissociation of Paf1 from RNA polymerase II. | Q27933085 | ||
The Paf1 complex physically and functionally associates with transcription elongation factors in vivo | Q27933848 | ||
The DNA damage checkpoint response requires histone H2B ubiquitination by Rad6-Bre1 and H3 methylation by Dot1. | Q27934025 | ||
A Requirement for the Saccharomyces cerevisiae Paf1 complex in snoRNA 3' end formation | Q27934649 | ||
The Saccharomyces cerevisiae RAD9, RAD17, RAD24 and MEC3 genes are required for tolerating irreparable, ultraviolet-induced DNA damage | Q27935475 | ||
Histone H2B ubiquitylation is associated with elongating RNA polymerase II | Q27936299 | ||
Molecular evidence indicating that the yeast PAF complex is required for transcription elongation | Q27936952 | ||
RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6. | Q27937381 | ||
Methylation of histone H3 lysine-79 by Dot1p plays multiple roles in the response to UV damage in Saccharomyces cerevisiae. | Q27937420 | ||
The transcription factor associated Ccr4 and Caf1 proteins are components of the major cytoplasmic mRNA deadenylase in Saccharomyces cerevisiae | Q27937565 | ||
A Rad26-Def1 complex coordinates repair and RNA pol II proteolysis in response to DNA damage | Q27937572 | ||
Regulation of histone modification and cryptic transcription by the Bur1 and Paf1 complexes | Q27938071 | ||
H2B ubiquitin protease Ubp8 and Sgf11 constitute a discrete functional module within the Saccharomyces cerevisiae SAGA complex. | Q27939759 | ||
The THP1-SAC3-SUS1-CDC31 complex works in transcription elongation-mRNA export preventing RNA-mediated genome instability. | Q27939828 | ||
The Paf1 complex is essential for histone monoubiquitination by the Rad6-Bre1 complex, which signals for histone methylation by COMPASS and Dot1p | Q27940017 | ||
A complex containing RNA polymerase II, Paf1p, Cdc73p, Hpr1p, and Ccr4p plays a role in protein kinase C signaling | Q27940291 | ||
Elongation by RNA polymerase II: the short and long of it | Q29614529 | ||
Histone ubiquitination: triggering gene activity | Q29617523 | ||
Distinction and relationship between elongation rate and processivity of RNA polymerase II in vivo | Q29619233 | ||
The SAGA continues: expanding the cellular role of a transcriptional co-activator complex | Q30438554 | ||
Spt4 modulates Rad26 requirement in transcription-coupled nucleotide excision repair | Q30973998 | ||
Initiation of DNA repair mediated by a stalled RNA polymerase IIO. | Q33231453 | ||
Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II | Q33551567 | ||
Transcription-coupled DNA repair in yeast transcription factor IIE (TFIIE) mutants | Q33614239 | ||
A posttranscriptional role for the yeast Paf1-RNA polymerase II complex is revealed by identification of primary targets. | Q53652090 | ||
A simple in vivo assay for measuring the efficiency of gene length-dependent processes in yeast mRNA biogenesis | Q82401286 | ||
The Saccharomyces cerevisiae RAD9 cell cycle checkpoint gene is required for optimal repair of UV-induced pyrimidine dimers in both G(1) and G(2)/M phases of the cell cycle | Q39085968 | ||
Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae. | Q39528577 | ||
Ultraviolet radiation-induced ubiquitination and proteasomal degradation of the large subunit of RNA polymerase II. Implications for transcription-coupled DNA repair | Q41056225 | ||
A chemical genomic screen in Saccharomyces cerevisiae reveals a role for diphthamidation of translation elongation factor 2 in inhibition of protein synthesis by sordarin | Q41876397 | ||
CAF1 plays an important role in mRNA deadenylation separate from its contact to CCR4. | Q42025763 | ||
Regulation of histone H3K4 tri-methylation and PAF complex recruitment by the Ccr4-Not complex | Q42747908 | ||
Screening the yeast "disruptome" for mutants affecting resistance to the immunosuppressive drug, mycophenolic acid | Q43997248 | ||
Phenotypic analysis of Paf1/RNA polymerase II complex mutations reveals connections to cell cycle regulation, protein synthesis, and lipid and nucleic acid metabolism | Q44190695 | ||
H2B ubiquitylation plays a role in nucleosome dynamics during transcription elongation | Q46493188 | ||
Multiple mechanisms confining RNA polymerase II ubiquitylation to polymerases undergoing transcriptional arrest | Q46550839 | ||
DNA damage-induced Def1-RNA polymerase II interaction and Def1 requirement for polymerase ubiquitylation in vitro | Q47422023 | ||
Histone acetylation, chromatin remodelling, transcription and nucleotide excision repair in S. cerevisiae: studies with two model genes | Q50129981 | ||
Gcn5 promotes acetylation, eviction, and methylation of nucleosomes in transcribed coding regions. | Q53577981 | ||
The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. | Q33640104 | ||
Cells have distinct mechanisms to maintain protection against different reactive oxygen species: oxidative-stress-response genes | Q33695799 | ||
E. coli Transcription repair coupling factor (Mfd protein) rescues arrested complexes by promoting forward translocation | Q34135671 | ||
Rpb4 and Rpb9 mediate subpathways of transcription-coupled DNA repair in Saccharomyces cerevisiae | Q34207143 | ||
Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 | ||
Transcription-coupled repair: a complex affair | Q34421058 | ||
A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage | Q34430366 | ||
The Bur1/Bur2 complex is required for histone H2B monoubiquitination by Rad6/Bre1 and histone methylation by COMPASS. | Q34470200 | ||
Mechanisms of transcription-coupled DNA repair | Q34514438 | ||
Terminating the transcript: breaking up is hard to do. | Q34520033 | ||
Breaking barriers to transcription elongation | Q34561019 | ||
Ccr4-not complex mRNA deadenylase activity contributes to DNA damage responses in Saccharomyces cerevisiae | Q34570125 | ||
The CCR4-NOT complex plays diverse roles in mRNA metabolism | Q35185687 | ||
The eukaryotic Ccr4-not complex: a regulatory platform integrating mRNA metabolism with cellular signaling pathways? | Q35805081 | ||
Diverse roles for histone H2A modifications in DNA damage response pathways in yeast | Q35844894 | ||
Yeast Rpb9 plays an important role in ubiquitylation and degradation of Rpb1 in response to UV-induced DNA damage | Q35948156 | ||
SAGA unveiled. | Q36011032 | ||
Bur1/Bur2 and the Ctk complex in yeast: the split personality of mammalian P-TEFb | Q36487341 | ||
Ccr4 alters cell size in yeast by modulating the timing of CLN1 and CLN2 expression | Q36665844 | ||
Contending with transcriptional arrest during RNAPII transcript elongation | Q36756252 | ||
Mediator complexes and eukaryotic transcription regulation: an overview | Q36942779 | ||
Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus | Q37144184 | ||
Members of the SAGA and Mediator complexes are partners of the transcription elongation factor TFIIS. | Q37592638 | ||
Genome-wide occupancy profile of mediator and the Srb8-11 module reveals interactions with coding regions | Q38314041 | ||
Defective Kin28, a subunit of yeast TFIIH, impairs transcription-coupled but not global genome nucleotide excision repair. | Q38329870 | ||
The structure and function of RAD6 and RAD18 DNA repair genes of Saccharomyces cerevisiae | Q38778956 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 2 | |
P304 | page(s) | e1000364 | |
P577 | publication date | 2009-02-06 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | Genome-wide analysis of factors affecting transcription elongation and DNA repair: a new role for PAF and Ccr4-not in transcription-coupled repair | |
P478 | volume | 5 |
Q35049516 | A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture |
Q33963920 | Abasic sites in the transcribed strand of yeast DNA are removed by transcription-coupled nucleotide excision repair |
Q51584347 | Beyond the known functions of the CCR4-NOT complex in gene expression regulatory mechanisms: New structural insights to unravel CCR4-NOT mRNA processing machinery. |
Q102152417 | Causes and consequences of RNA polymerase II stalling during transcript elongation |
Q35573001 | Ccr4-Not and TFIIS Function Cooperatively To Rescue Arrested RNA Polymerase II |
Q26823940 | Ccr4-Not complex: the control freak of eukaryotic cells |
Q92858958 | Ccr4-Not maintains genomic integrity by controlling the ubiquitylation and degradation of arrested RNAPII |
Q28545102 | Ccr4-not regulates RNA polymerase I transcription and couples nutrient signaling to the control of ribosomal RNA biogenesis |
Q27936277 | Cleavage factor I links transcription termination to DNA damage response and genome integrity maintenance in Saccharomyces cerevisiae |
Q28709604 | DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae |
Q38336126 | DUBs, the regulation of cell identity and disease |
Q50994474 | Def1 and Dst1 play distinct roles in repair of AP lesions in highly transcribed genomic regions. |
Q49587821 | Def1 interacts with TFIIH and modulates RNA polymerase II transcription. |
Q34477635 | Defining Genetic Factors That Modulate Intergenerational CAG Repeat Instability inDrosophila melanogaster |
Q27934457 | Diverse roles of RNA polymerase II-associated factor 1 complex in different subpathways of nucleotide excision repair |
Q38820585 | Dual roles of DNA repair enzymes in RNA biology/post-transcriptional control |
Q52328152 | Functional diversification accompanies gene family expansion of MED2 homologs in Candida albicans. |
Q91828974 | Functional interplay between Mediator and RNA polymerase II in Rad2/XPG loading to the chromatin |
Q35691209 | Genome-wide screen of fission yeast mutants for sensitivity to 6-azauracil, an inhibitor of transcriptional elongation |
Q37388888 | Mediator links transcription and DNA repair by facilitating Rad2/XPG recruitment |
Q40465734 | Npl3, a new link between RNA-binding proteins and the maintenance of genome integrity. |
Q38028210 | One step back before moving forward: regulation of transcription elongation by arrest and backtracking. |
Q27937614 | Overexpression of SNG1 causes 6-azauracil resistance in Saccharomyces cerevisiae. |
Q58726157 | Paf1 and Ctr9 subcomplex formation is essential for Paf1 complex assembly and functional regulation |
Q34552148 | Proteomic Analysis of the Mediator Complex Interactome in Saccharomyces cerevisiae |
Q43158336 | RNA polymerase II contributes to preventing transcription-mediated replication fork stalls |
Q36029959 | RNF20 and USP44 regulate stem cell differentiation by modulating H2B monoubiquitylation |
Q33749402 | Regulatory mechanisms of RNA function: emerging roles of DNA repair enzymes. |
Q35917402 | Role of Mediator in regulating Pol II elongation and nucleosome displacement in Saccharomyces cerevisiae |
Q92204734 | Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance |
Q38636948 | Stimulation of RNA Polymerase II ubiquitination and degradation by yeast mRNA 3'-end processing factors is a conserved DNA damage response in eukaryotes. |
Q28714380 | Sub1 associates with Spt5 and influences RNA polymerase II transcription elongation rate |
Q26773045 | The Ccr4-Not complex is a key regulator of eukaryotic gene expression |
Q28299679 | The Mediator complex and transcription regulation |
Q42116049 | The Npl3 hnRNP prevents R-loop-mediated transcription-replication conflicts and genome instability |
Q34580247 | The Rpb4/7 module of RNA polymerase II is required for carbon catabolite repressor protein 4-negative on TATA (Ccr4-not) complex to promote elongation |
Q37405368 | The cellular roles of Ccr4-NOT in model and pathogenic fungi-implications for fungal virulence |
Q36532642 | The control of elongation by the yeast Ccr4-not complex |
Q28749801 | The distribution of active RNA polymerase II along the transcribed region is gene-specific and controlled by elongation factors |
Q36522035 | The many roles of the conserved eukaryotic Paf1 complex in regulating transcription, histone modifications, and disease states |
Q27933267 | The multifunctional Ccr4-Not complex directly promotes transcription elongation |
Q34122297 | The nuclear pore complex: bridging nuclear transport and gene regulation |
Q27934407 | The prefoldin complex regulates chromatin dynamics during transcription elongation |
Q26801362 | Transcription Blockage Leads to New Beginnings |
Q39042789 | Transcription factors that influence RNA polymerases I and II: To what extent is mechanism of action conserved? |
Q42133855 | Transcriptional elongation and mRNA export are coregulated processes. |
Q33635923 | Wide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo |