The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Signaling Pathways Differentially Affect RNA Polymerase II Initiation, Pausing, and Elongation Rate in Cells
Open accessAbstract
RNA polymerase II (Pol II) transcribes hundreds of kilobases of DNA, limiting the production of mRNAs and lncRNAs. We used global run-on sequencing (GRO-seq) to measure the rates of transcription by Pol II following gene activation. Elongation rates vary as much as 4-fold at different genomic loci and in response to two distinct cellular signaling pathways (i.e., 17β-estradiol [E2] and TNF-α). The rates are slowest near the promoter and increase during the first ~15 kb transcribed. Gene body elongation rates correlate with Pol II density, resulting in systematically higher rates of transcript production at genes with higher Pol II density. Pol II dynamics following short inductions indicate that E2 stimulates gene expression by increasing Pol II initiation, whereas TNF-α reduces Pol II residence time at pause sites. Collectively, our results identify previously uncharacterized variation in the rate of transcription and highlight elongation as an important, variable, and regulated rate-limiting step during transcription.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“All these techniques showed in various human cell lines that the average RNA Pol II speed ranges between 1.25 kb/min and 3.5 kb/min (Danko et al, 2013; Fuchs et al, 2014b; Jonkers et al, 2014; Saponaro et al, 2014; Veloso et al, 2014; Liang et al, 2018; Baluapuri et al, 2019; Gregersen et al, 2020).”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Danko et al, 2013
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“RNA Pol II speed was furthermore also shown to be highly variable within individual genes, as RNA Pol II accelerates while traveling throughout the gene body, starting at 0.5 kb/min in the first 10–15 kb and accelerating up to 2–4 kb/min downstream (Danko et al, 2013; Fuchs et al, 2014b; Jonkers et al, 2014; Saponaro et al, 2014).”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Danko et al, 2013
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Contrary to what had been initially shown for a few genes (Singh & Padgett, 2009; Wada et al, 2009), the measured transcription speed was found to be extremely variable between genes, with RNA Pol II velocity varying from 0.37 kb/min to 3.57 kb/min for individual genes (Danko et al, 2013).”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Danko et al, 2013
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“However, Danko et al (2013) found that RNA Pol II velocity can differ by as much as 25–40% on individual genes in different cell lines and in response to diverse signaling pathways.”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Danko et al, 2013
The cited source says what the claim attributes to it.
In the citing paper
“Indeed, genes with the highest measured RNA Pol II velocity have been shown to generate more mRNAs (Danko et al, 2013; Jonkers et al, 2014; Cohen et al, 2018).”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Danko et al, 2013
The cited source says what the claim attributes to it.
In the citing paper
“First, RNA Pol II velocity differs by as much as 25–40% on individual genes stimulated by diverse signaling pathways in different cell lines (Danko et al, 2013).”
From RNA polymerase II speed: a key player in controlling and adapting transcriptome composition (2021) · cites this paper as Danko et al, 2013
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
High-Resolution Profiling of Histone Methylations in the Human Genome
Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845
Nascent RNA Sequencing Reveals Widespread Pausing and Divergent Initiation at Human Promoters
Core, L. J., Waterfall, J. J., & Lis, J. T. (2008) · Science · doi:10.1126/science.1162228 · Cited by 1,986
Self-citationStochastic mRNA Synthesis in Mammalian Cells
Raj, A., Peskin, C. S., Tranchina, D., Vargas, D. Y., & Tyagi, S. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040309 · Cited by 1,737
Dynamic Regulation of Nucleosome Positioning in the Human Genome
Schones, D. E., Cui, K., Cuddapah, S., Roh, T., Barski, A., Wang, Z., Wei, G., & Zhao, K. (2008) · Cell · doi:10.1016/j.cell.2008.02.022 · Cited by 1,473
Genome-wide analysis of estrogen receptor binding sites
Carroll, J. S., Meyer, C. A., Song, J. S., Li, W., Geistlinger, T., Eeckhoute, J., Brodsky, A. S., Keeton, E. K., Fertuck, K. C., Hall, G., et al. (2006) · Nature Genetics · doi:10.1038/ng1901 · Cited by 1,397
FACT Facilitates Transcription-Dependent Nucleosome Alteration
Belotserkovskaya, R., Oh, S., Bondarenko, V. A., Orphanides, G., Studitsky, V. M., & Reinberg, D. (2003) · Science · doi:10.1126/science.1085703 · Cited by 869
Reprogramming transcription by distinct classes of enhancers functionally defined by eRNA
Wang, D., García-Bassets, I., Benner, C. W., Li, W., Su, X. B., Zhou, Y., Qiu, J., Liu, W., Kaikkonen, M. U., Ohgi, K. A., et al. (2011) · Nature · doi:10.1038/nature10006 · Cited by 854
Yamaguchi, Y., Takagi, T., Wada, T., Yano, K., Furuya, A., Sugimoto, S., Hasegawa, J., & Handa, H. (1999) · Cell · doi:10.1016/s0092-8674(00)80713-8 · Cited by 841
Control of Inducible Gene Expression by Signal-Dependent Transcriptional Elongation
Hargreaves, D. C., Horng, T., & Medzhitov, R. M. (2009) · Journal of End-to-End-testing · doi:10.1016/j.cell.2009.05.047 · Cited by 676
In vivo dynamics of RNA polymerase II transcription
Darzacq, X., Shav-Tal, Y., de Turris, V., Brody, Y., Shenoy, S. M., Phair, R. D., & Singer, R. H. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1280 · Cited by 665
Defining mechanisms that regulate RNA polymerase II transcription in vivo
Fuda, N. J., Ardehali, M. B., & Lis, J. T. (2009) · Nature · doi:10.1038/nature08449 · Cited by 576
Self-citationDynamics of Replication-Independent Histone Turnover in Budding Yeast
Dion, M. F., Kaplan, T., Kim, M., Buratowski, S., Friedman, N., & Rando, O. J. (2007) · Science · doi:10.1126/science.1134053 · Cited by 556
Hah, N., Danko, C. G., Core, L. J., Waterfall, J. J., Siepel, A. C., Lis, J. T., & Kraus, W. L. (2011) · Cell · doi:10.1016/j.cell.2011.03.042 · Cited by 503
Self-citationThe genomic landscape of histone modifications in human T cells
Roh, T., Cuddapah, S., Cui, K., & Zhao, K. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607617103 · Cited by 499
Genome-wide kinetics of nucleosome turnover determined by metabolic labeling of histones
Deal, R., Henikoff, J., & Henikoff, S. (2010) · Science · doi:10.1126/science.1186777 · Cited by 493
Rates of in situ transcription and splicing in large human genes
Singh, J., & Padgett, R. A. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1666 · Cited by 487
Uniform transitions of the general RNA polymerase II transcription complex
Mayer, A., Lidschreiber, M., Siebert, M., Leike, K., Söding, J., & Cramer, P. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1903 · Cited by 446
NF-κB Binds P-TEFb to Stimulate Transcriptional Elongation by RNA Polymerase II
Barborič, M., Nissen, R. M., Kanazawa, S., Jabrane‐Ferrat, N., & Peterlin, B. M. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00314-8 · Cited by 434
ChIP‐Seq of ERα and RNA polymerase II defines genes differentially responding to ligands
Welboren, W.-J., van Driel, M. A., Janssen‐Megens, E. M., van Heeringen, S. J., Sweep, F. C. G. J., Span, P. N., & Stunnenberg, H. G. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.88 · Cited by 395
Kraus, W. L., & Kadonaga, J. T. (1998) · Genes & Development · doi:10.1101/gad.12.3.331 · Cited by 334
Self-citationSynchronous and Stochastic Patterns of Gene Activation in the Drosophila Embryo
Boettiger, A. N., & Levine, M. (2009) · Science · doi:10.1126/science.1173976 · Cited by 256
Smith, E. R., & Shilatifard, A. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.11.031 · Cited by 242
Cooperation Between RNA Polymerase Molecules in Transcription Elongation
Epshtein, V., & Nudler, E. (2003) · Science · doi:10.1126/science.1083219 · Cited by 234
Izban, M. G., & Luse, D. S. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42262-4 · Cited by 233
Transcriptional Activators Differ in Their Abilities to Control Alternative Splicing
Nogués, G., Kadener, S., Cramer, P., Bentley, D. L., & Kornblihtt, A. R. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m208418200 · Cited by 189
Lin, C., Garrett, A. S., Kumar, B. D., Smith, E. R., Gogol, M., Seidel, C. W., Krumlauf, R. K., & Shilatifard, A. (2011) · Genes & Development · doi:10.1101/gad.2059211 · Cited by 187
Kininis, M., Chen, B. S., Diehl, A. G., Isaacs, G. D., Zhang, T., Siepel, A. C., Clark, A. G., & Kraus, W. L. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00083-07 · Cited by 186
Self-citationPromoter-associated Pausing in Promoter Architecture and Postinitiation Transcriptional RegulationPreprint
Lis, J. T. (1998) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1998.63.347 · Cited by 172
Self-citationA wave of nascent transcription on activated human genes
Wada, Y., Ohta, Y., Xu, M., Tsutsumi, S., Minami, T., Inoue, K., Komura, D., Kitakami, J.-I., Oshida, N., Papantonis, A., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902573106 · Cited by 154
Acetylation of Histone H3 at the Nucleosome Dyad Alters DNA-Histone Binding
Manohar, M., Mooney, A. M., North, J. A., Nakkula, R. J., Picking, J. W., Edon, A., Fishel, R. A., Poirier, M. G., & Ottesen, J. J. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.003202 · Cited by 138
Gilchrist, D. A., Fromm, G. J., dos Santos, G., Pham, L. N., McDaniel, I. E., Burkholder, A., Fargo, D. C., & Adelman, K. (2012) · Genes & Development · doi:10.1101/gad.187781.112 · Cited by 138
Zhou, H.-L., Hinman, M. N., Barron, V. A., Geng, C., Zhou, G., Luo, G., Siegel, R. E., & Lou, H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103344108 · Cited by 136
RNA polymerase II kinetics in polo polyadenylation signal selection
Pinto, P. A. B., Henriques, T., Freitas, M. O., Martins, T., Domingues, R. G., Wyrzykowska, P. S., Coelho, P. A., Carmo, A. M., Sunkel, C. E., Proudfoot, N. J., et al. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.156 · Cited by 136
Tracking rates of transcription and splicing in vivo
Ardehali, M. B., & Lis, J. T. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1109-1123 · Cited by 125
Self-citationCastle, J. C., Armour, C. D., Löwer, M., Haynor, D. R., Biery, M. C., Bouzek, H. K., Chen, R., Jackson, S., Johnson, J. M., Rohl, C. A., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011779 · Cited by 124
Stability, Flexibility, and Dynamic Interactions of Colliding RNA Polymerase II Elongation Complexes
Saeki, H., & Svejstrup, J. Q. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.06.009 · Cited by 92
Kininis, M., Isaacs, G. D., Core, L. J., Hah, N., & Kraus, W. L. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00841-08 · Cited by 88
Self-citationCoactivator Function Defines the Active Estrogen Receptor Alpha Cistrome
Lupien, M., Eeckhoute, J., Meyer, C. A., Krum, S. A., Rhodes, D. R., Liu, X., & Brown, M. A. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00020-09 · Cited by 76
Cited by
Sorted by citations
Getting up to speed with transcription elongation by RNA polymerase II
Jonkers, I., & Lis, J. T. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3953 · Cited by 876
Self-citationCoupling mRNA processing with transcription in time and space
Bentley, D. L. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3662 · Cited by 828
Jonkers, I., Kwak, H., & Lis, J. T. (2014) · eLife · doi:10.7554/elife.02407 · Cited by 581
Self-citationPromoter-proximal pausing of RNA polymerase II: a nexus of gene regulationPreprint
Core, L. J., & Adelman, K. (2019) · Genes & Development · doi:10.1101/gad.325142.119 · Cited by 611
Self-citationTranscription Elongation Can Affect Genome 3D Structure
Heinz, S., Texari, L., Hayes, M. G. B., Urbanowski, M., Chang, M. W., Givarkes, N., Rialdi, A., White, K. M., Albrecht, R. A., Pache, L., et al. (2018) · Cell · doi:10.1016/j.cell.2018.07.047 · Cited by 453
Metadata
- Authors
- Danko, C. G., Hah, N., Luo, X., Martins, A. L., Core, L., Lis, J. T., Siepel, A., & Kraus, W. L.
- Affiliations
- Cornell University (US)
- Corresponding author
- Kraus, W. Lee
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2013-04
- Volume
- 50
- Issue
- 2
- Pages
- 212-222
- ISSN
- 1097-2765 (ISSN-L)
- PMC
- PMC3640649
- OpenAlex
- W2016349604
- Cited by
- 333
- References
- 38
- Citations by year
- 2026: 9 · 2025: 17 · 2024: 21 · 2023: 15 · 2022: 20 · 2021: 34 · 2020: 21 · 2019: 27 · 2018: 32 · 2017: 25 · 2016: 34 · 2015: 33 · 2014: 29 · 2013: 16
- FWCI
- 17.16
- Type
- journal article
- Language
- en
- Update notices
- erratum (2013-06-06)
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Funders
- U.S. Department of Defense
- Pharmaceutical Research and Manufacturers of America Foundation
- National Institutes of Health
- National Institute of General Medical Sciences (R01GM025232, R37GM025232, GM-25232)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK058110, R01DK058110)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD052471)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- RNA polymerase II, transcription elongation, transcription initiation, RNA polymerase II pausing, elongation rate, estradiol, TNF-α, gene activation, pause sites, gene body, signaling pathways, transcriptional regulation
- MeSH terms
- Estradiol, Humans, Kinetics, Promoter Regions, Genetic, RNA Polymerase II, RNA, Messenger, Transcription Factors, Transcription, Genetic, Tumor Necrosis Factor-alpha, Signal Transduction, Transcriptional Activation, Transcription Initiation Site, Transcriptome, Transcription Initiation, Genetic, MCF-7 Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review