| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2012PLoSO...738769A |
| P356 | DOI | 10.1371/JOURNAL.PONE.0038769 |
| P932 | PMC publication ID | 3372504 |
| P698 | PubMed publication ID | 22701709 |
| P5875 | ResearchGate publication ID | 225372578 |
| P2093 | author name string | Olivier Poch | |
| Laetitia Poidevin | |||
| Làszlò Tora | |||
| Krishanpal Anamika | |||
| Àkos Gyenis | |||
| P2860 | cites work | Evolutionarily conserved interaction between CstF-64 and PC4 links transcription, polyadenylation, and termination | Q24291290 |
| Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination | Q24307617 | ||
| Human 5' --> 3' exonuclease Xrn2 promotes transcription termination at co-transcriptional cleavage sites | Q24317135 | ||
| Pause sites promote transcriptional termination of mammalian RNA polymerase II | Q24548945 | ||
| NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins | Q24558592 | ||
| c-Myc regulates transcriptional pause release | Q24629119 | ||
| RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo | Q24645367 | ||
| Poly(A) signal-dependent degradation of unprocessed nascent transcripts accompanies poly(A) signal-dependent transcriptional pausing in vitro | Q24650853 | ||
| The multifunctional protein p54nrb/PSF recruits the exonuclease XRN2 to facilitate pre-mRNA 3' processing and transcription termination | Q24671920 | ||
| WebGestalt: an integrated system for exploring gene sets in various biological contexts | Q24813284 | ||
| The yeast Rat1 exonuclease promotes transcription termination by RNA polymerase II. | Q27934493 | ||
| Promoter-associated pausing in promoter architecture and postinitiation transcriptional regulation | Q28138307 | ||
| Multiple transcript cleavage precedes polymerase release in termination by RNA polymerase II | Q28199201 | ||
| Diversified transcription initiation complexes expand promoter selectivity and tissue-specific gene expression | Q28208297 | ||
| Transcription factor TFIID recruits factor CPSF for formation of 3' end of mRNA | Q28249862 | ||
| Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail | Q28297786 | ||
| The general transcription factors of RNA polymerase II | Q28298663 | ||
| Formation of the 3' end of histone mRNA | Q28610112 | ||
| Integrating mRNA processing with transcription | Q28610124 | ||
| Formation of the 3' end of histone mRNA: getting closer to the end | Q28751417 | ||
| Transcription termination by nuclear RNA polymerases | Q29541446 | ||
| A chromatin landmark and transcription initiation at most promoters in human cells | Q29547180 | ||
| Divergent transcription from active promoters | Q29614332 | ||
| RNA polymerase is poised for activation across the genome | Q29615047 | ||
| Transcriptional activation by recruitment | Q29615048 | ||
| seqMINER: an integrated ChIP-seq data interpretation platform | Q33777909 | ||
| The RNA polymerase II molecule at the 5' end of the uninduced hsp70 gene of D. melanogaster is transcriptionally engaged. | Q52459657 | ||
| An ending is a new beginning: transcription termination supports re-initiation. | Q53267577 | ||
| A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II | Q69827439 | ||
| Compensatory mutations suggest that base-pairing with a small nuclear RNA is required to form the 3' end of H3 messenger RNA | Q70151935 | ||
| Termination of transcription in the mouse alpha-amylase gene Amy-2a occurs at multiple sites downstream of the polyadenylation site | Q72396715 | ||
| Terminal exon definition occurs cotranscriptionally and promotes termination of RNA polymerase II | Q77308193 | ||
| The polyadenylation inhibitor cordycepin (3'dA) causes a decline in c-MYC mRNA levels without affecting c-MYC protein levels | Q77931499 | ||
| Generation of histone mRNA 3' ends by endonucleolytic cleavage of the pre-mRNA in a snRNP-dependent in vitro reaction | Q33879922 | ||
| RNA polymerase II pauses and associates with pre-mRNA processing factors at both ends of genes. | Q34009055 | ||
| On the importance of being co-transcriptional | Q34150533 | ||
| Ending the message: poly(A) signals then and now | Q34213955 | ||
| A poly(A) addition site and a downstream termination region are required for efficient cessation of transcription by RNA polymerase II in the mouse beta maj-globin gene | Q34369553 | ||
| Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 | ||
| The role of Rat1 in coupling mRNA 3'-end processing to transcription termination: implications for a unified allosteric-torpedo model | Q34511126 | ||
| Novel role for mediator complex subunit Srb5/Med18 in termination of transcription | Q35423214 | ||
| Ultrastructural study of transcription factories in mouse erythroblasts | Q35548402 | ||
| New perspectives on connecting messenger RNA 3' end formation to transcription | Q35774183 | ||
| Connections between mRNA 3' end processing and transcription termination | Q36131487 | ||
| Global analysis of short RNAs reveals widespread promoter-proximal stalling and arrest of Pol II in Drosophila | Q36214878 | ||
| An intact histone 3'-processing site is required for transcription termination in a mouse histone H2a gene | Q36681497 | ||
| NELF and GAGA factor are linked to promoter-proximal pausing at many genes in Drosophila | Q36710845 | ||
| Polycomb associates genome-wide with a specific RNA polymerase II variant, and regulates metabolic genes in ESCs | Q36927892 | ||
| Control of eukaryotic gene expression: gene loops and transcriptional memory. | Q37805178 | ||
| A genomic analysis of RNA polymerase II modification and chromatin architecture related to 3' end RNA polyadenylation | Q38290836 | ||
| MAZ-dependent termination between closely spaced human complement genes | Q38301674 | ||
| Specific transcriptional pausing activates polyadenylation in a coupled in vitro system | Q38323992 | ||
| Transcription regulation through promoter-proximal pausing of RNA polymerase II. | Q39442921 | ||
| Mechanism of poly(A) signal transduction to RNA polymerase II in vitro | Q39528777 | ||
| A rapid, extensive, and transient transcriptional response to estrogen signaling in breast cancer cells | Q39546838 | ||
| Multilevel regulation of replication-dependent histone genes | Q39569366 | ||
| TFIIH-associated Cdk7 kinase functions in phosphorylation of C-terminal domain Ser7 residues, promoter-proximal pausing, and termination by RNA polymerase II | Q39814573 | ||
| Phosphorylation of TFIIB links transcription initiation and termination. | Q39886347 | ||
| The two steps of poly(A)-dependent termination, pausing and release, can be uncoupled by truncation of the RNA polymerase II carboxyl-terminal repeat domain | Q40815653 | ||
| A pause site for RNA polymerase II is associated with termination of transcription | Q41081406 | ||
| Transcriptional termination between the closely linked human complement genes C2 and factor B: common termination factor for C2 and c-myc? | Q41083821 | ||
| A core complex of CPSF73, CPSF100, and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs | Q41656652 | ||
| Characterization of the mouse beta maj globin transcription termination region: a spacing sequence is required between the poly(A) signal sequence and multiple downstream termination elements | Q41817304 | ||
| Functional interaction of the Ess1 prolyl isomerase with components of the RNA polymerase II initiation and termination machineries | Q41837167 | ||
| The conserved AAUAAA hexamer of the poly(A) signal can act alone to trigger a stable decrease in RNA polymerase II transcription velocity | Q41875673 | ||
| Gene looping is conferred by activator-dependent interaction of transcription initiation and termination machineries | Q42035394 | ||
| Biased chromatin signatures around polyadenylation sites and exons | Q42689954 | ||
| Crosstalk between mRNA 3' end processing and transcription initiation | Q42821628 | ||
| The poly(A) signal, without the assistance of any downstream element, directs RNA polymerase II to pause in vivo and then to release stochastically from the template | Q46370210 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e38769 | |
| P577 | publication date | 2012-06-11 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | RNA polymerase II pausing downstream of core histone genes is different from genes producing polyadenylated transcripts | |
| P478 | volume | 7 |
| Q41983938 | 3' end formation of pre-mRNA and phosphorylation of Ser2 on the RNA polymerase II CTD are reciprocally coupled in human cells |
| Q34042569 | A novel role for the Pol I transcription factor UBTF in maintaining genome stability through the regulation of highly transcribed Pol II genes |
| Q28596144 | A subset of replication-dependent histone mRNAs are expressed as polyadenylated RNAs in terminally differentiated tissues |
| Q47863733 | Birth and Death of Histone mRNAs |
| Q38890103 | CDK9 inhibitors define elongation checkpoints at both ends of RNA polymerase II-transcribed genes. |
| Q39114351 | Chromatin loop organization of the junb locus in mouse dendritic cells |
| Q36976457 | Concentrating pre-mRNA processing factors in the histone locus body facilitates efficient histone mRNA biogenesis. |
| Q47110577 | Coordinating cell cycle-regulated histone gene expression through assembly and function of the Histone Locus Body |
| Q38822658 | Coordination of RNA Polymerase II Pausing and 3' End Processing Factor Recruitment with Alternative Polyadenylation. |
| Q37508064 | Divergent transcription: a driving force for new gene origination? |
| Q38827412 | Effects of Transcription Elongation Rate and Xrn2 Exonuclease Activity on RNA Polymerase II Termination Suggest Widespread Kinetic Competition. |
| Q42083039 | Enhancer regions show high histone H3.3 turnover that changes during differentiation |
| Q26798138 | Fail-safe transcription termination: Because one is never enough |
| Q89393350 | Heat Shock Causes a Reversible Increase in RNA Polymerase II Occupancy Downstream of mRNA Genes, Consistent with a Global Loss in Transcriptional Termination |
| Q34310275 | How to stop: the mysterious links among RNA polymerase II occupancy 3' of genes, mRNA 3' processing and termination |
| Q37593366 | Human p53 interacts with the elongating RNAPII complex and is required for the release of actinomycin D induced transcription blockage |
| Q37174524 | Localization of RNAPII and 3' end formation factor CstF subunits on C. elegans genes and operons |
| Q38085601 | Making ends meet: coordination between RNA 3'-end processing and transcription initiation. |
| Q37379794 | Nascent RNA sequencing reveals distinct features in plant transcription |
| Q54420293 | Polyadenylation site-induced decay of upstream transcripts enforces promoter directionality. |
| Q102210876 | Proteomic profiling and genome-wide mapping of O-GlcNAc chromatin-associated proteins reveal an O-GlcNAc-regulated genotoxic stress response |
| Q48268876 | The RNA exosome promotes transcription termination of backtracked RNA polymerase II. |
| Q40090160 | The point of no return: The poly(A)-associated elongation checkpoint |
| Q87887544 | Transcription elongation rate affects nascent histone pre-mRNA folding and 3' end processing |
| Q34308284 | Transcription termination by the eukaryotic RNA polymerase III. |
| Q33945643 | UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells |
| Q35233598 | Vertebrate Ssu72 regulates and coordinates 3'-end formation of RNAs transcribed by RNA polymerase II. |
| Q90025192 | Widespread Backtracking by RNA Pol II Is a Major Effector of Gene Activation, 5' Pause Release, Termination, and Transcription Elongation Rate |
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