308 related articles for article (PubMed ID: 29304333)
21. Stress-induced transcriptional memory accelerates promoter-proximal pause release and decelerates termination over mitotic divisions.
Vihervaara A; Mahat DB; Himanen SV; Blom MAH; Lis JT; Sistonen L
Mol Cell; 2021 Apr; 81(8):1715-1731.e6. PubMed ID: 33784494
[TBL] [Abstract][Full Text] [Related]
22. Tyrosine 1-phosphorylated RNA polymerase II transcribes PROMPTs to facilitate proximal promoter pausing and induce global transcriptional repression in response to DNA damage.
Ajit K; Alagia A; Burger K; Gullerova M
Genome Res; 2024 Mar; 34(2):201-216. PubMed ID: 38467418
[TBL] [Abstract][Full Text] [Related]
23. Elongation/Termination Factor Exchange Mediated by PP1 Phosphatase Orchestrates Transcription Termination.
Kecman T; Kuś K; Heo DH; Duckett K; Birot A; Liberatori S; Mohammed S; Geis-Asteggiante L; Robinson CV; Vasiljeva L
Cell Rep; 2018 Oct; 25(1):259-269.e5. PubMed ID: 30282034
[TBL] [Abstract][Full Text] [Related]
24. Herpes Simplex Virus 1 Dramatically Alters Loading and Positioning of RNA Polymerase II on Host Genes Early in Infection.
Birkenheuer CH; Danko CG; Baines JD
J Virol; 2018 Apr; 92(8):. PubMed ID: 29437966
[TBL] [Abstract][Full Text] [Related]
25. RNA polymerase II activity revealed by GRO-seq and pNET-seq in Arabidopsis.
Zhu J; Liu M; Liu X; Dong Z
Nat Plants; 2018 Dec; 4(12):1112-1123. PubMed ID: 30374093
[TBL] [Abstract][Full Text] [Related]
26. Basal components of the transcription apparatus (RNA polymerase II, TATA-binding protein) contain activation domains: is the repetitive C-terminal domain (CTD) of RNA polymerase II a "portable enhancer domain"?
Seipel K; Georgiev O; Gerber HP; Schaffner W
Mol Reprod Dev; 1994 Oct; 39(2):215-25. PubMed ID: 7826625
[TBL] [Abstract][Full Text] [Related]
27. The C-Terminal Domain of RNA Polymerase II Is a Multivalent Targeting Sequence that Supports Drosophila Development with Only Consensus Heptads.
Lu F; Portz B; Gilmour DS
Mol Cell; 2019 Mar; 73(6):1232-1242.e4. PubMed ID: 30765194
[TBL] [Abstract][Full Text] [Related]
28. Serine-7 of the RNA polymerase II CTD is specifically required for snRNA gene expression.
Egloff S; O'Reilly D; Chapman RD; Taylor A; Tanzhaus K; Pitts L; Eick D; Murphy S
Science; 2007 Dec; 318(5857):1777-9. PubMed ID: 18079403
[TBL] [Abstract][Full Text] [Related]
29. Phospho-site mutants of the RNA Polymerase II C-terminal domain alter subtelomeric gene expression and chromatin modification state in fission yeast.
Inada M; Nichols RJ; Parsa JY; Homer CM; Benn RA; Hoxie RS; Madhani HD; Shuman S; Schwer B; Pleiss JA
Nucleic Acids Res; 2016 Nov; 44(19):9180-9189. PubMed ID: 27402158
[TBL] [Abstract][Full Text] [Related]
30. The Integrator Complex Attenuates Promoter-Proximal Transcription at Protein-Coding Genes.
Elrod ND; Henriques T; Huang KL; Tatomer DC; Wilusz JE; Wagner EJ; Adelman K
Mol Cell; 2019 Dec; 76(5):738-752.e7. PubMed ID: 31809743
[TBL] [Abstract][Full Text] [Related]
31. PRO-IP-seq tracks molecular modifications of engaged Pol II complexes at nucleotide resolution.
Vihervaara A; Versluis P; Himanen SV; Lis JT
Nat Commun; 2023 Nov; 14(1):7039. PubMed ID: 37923726
[TBL] [Abstract][Full Text] [Related]
32. Live-cell analysis of endogenous GFP-RPB1 uncovers rapid turnover of initiating and promoter-paused RNA Polymerase II.
Steurer B; Janssens RC; Geverts B; Geijer ME; Wienholz F; Theil AF; Chang J; Dealy S; Pothof J; van Cappellen WA; Houtsmuller AB; Marteijn JA
Proc Natl Acad Sci U S A; 2018 May; 115(19):E4368-E4376. PubMed ID: 29632207
[TBL] [Abstract][Full Text] [Related]
33. The integrator complex recognizes a new double mark on the RNA polymerase II carboxyl-terminal domain.
Egloff S; Szczepaniak SA; Dienstbier M; Taylor A; Knight S; Murphy S
J Biol Chem; 2010 Jul; 285(27):20564-9. PubMed ID: 20457598
[TBL] [Abstract][Full Text] [Related]
34. RNA polymerase II accumulation in the promoter-proximal region of the dihydrofolate reductase and gamma-actin genes.
Cheng C; Sharp PA
Mol Cell Biol; 2003 Mar; 23(6):1961-7. PubMed ID: 12612070
[TBL] [Abstract][Full Text] [Related]
35. The last CTD repeat of the mammalian RNA polymerase II large subunit is important for its stability.
Chapman RD; Palancade B; Lang A; Bensaude O; Eick D
Nucleic Acids Res; 2004; 32(1):35-44. PubMed ID: 14704341
[TBL] [Abstract][Full Text] [Related]
36. Control of Gene Expression in Senescence through Transcriptional Read-Through of Convergent Protein-Coding Genes.
Muniz L; Deb MK; Aguirrebengoa M; Lazorthes S; Trouche D; Nicolas E
Cell Rep; 2017 Nov; 21(9):2433-2446. PubMed ID: 29186682
[TBL] [Abstract][Full Text] [Related]
37. Conditional expression of RNA polymerase II in mammalian cells. Deletion of the carboxyl-terminal domain of the large subunit affects early steps in transcription.
Meininghaus M; Chapman RD; Horndasch M; Eick D
J Biol Chem; 2000 Aug; 275(32):24375-82. PubMed ID: 10825165
[TBL] [Abstract][Full Text] [Related]
38. Transcription of Mammalian cis-Regulatory Elements Is Restrained by Actively Enforced Early Termination.
Austenaa LM; Barozzi I; Simonatto M; Masella S; Della Chiara G; Ghisletti S; Curina A; de Wit E; Bouwman BA; de Pretis S; Piccolo V; Termanini A; Prosperini E; Pelizzola M; de Laat W; Natoli G
Mol Cell; 2015 Nov; 60(3):460-74. PubMed ID: 26593720
[TBL] [Abstract][Full Text] [Related]
39. RNA polymerase II pausing as a context-dependent reader of the genome.
Scheidegger A; Nechaev S
Biochem Cell Biol; 2016 Feb; 94(1):82-92. PubMed ID: 26555214
[TBL] [Abstract][Full Text] [Related]
40. Integrator is a genome-wide attenuator of non-productive transcription.
Lykke-Andersen S; Žumer K; Molska EŠ; Rouvière JO; Wu G; Demel C; Schwalb B; Schmid M; Cramer P; Jensen TH
Mol Cell; 2021 Feb; 81(3):514-529.e6. PubMed ID: 33385327
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
