Evidence map›Paper›PMID 27729537›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Backtracked and paused transcription initiation intermediate of Escherichia coli RNA polymerase.

Eitan Lerner, SangYoon Chung, Benjamin L Allen, Shuang Wang, Jookyung Lee, Shijia W Lu, Logan W Grimaud, Antonino Ingargiola, Xavier Michalet, Yazan Alhadid and 4 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 89 citations in OpenAlex.

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  17. Structural and mechanistic basis of σ-dependent transcriptional pausing.Proceedings of the National Academy of Sciences of the United States of America · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Eitan LernerDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.
SangYoon ChungDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.
Benjamin L AllenDepartment of Chemistry & Biochemistry, University of Colorado, Boulder, CO 80309.
Shuang WangInstitut Jacques Monod, Centre National de la Recherche Scientifique (CNRS), UMR7592, University Paris Diderot, Sorbonne Paris Cité, F-75205 Paris, France.
Jookyung LeeRowan University School of Osteopathic Medicine, Stratford, NJ 08084.
Shijia W LuDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.
Logan W GrimaudDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.
Antonino IngargiolaDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.ORCID 0000-0002-9348-1397
Xavier MichaletDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.
Yazan AlhadidDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.
Sergei BorukhovRowan University School of Osteopathic Medicine, Stratford, NJ 08084.
Terence R StrickInstitut Jacques Monod, Centre National de la Recherche Scientifique (CNRS), UMR7592, University Paris Diderot, Sorbonne Paris Cité, F-75205 Paris, France; Institut de Biologie de l'Ecole Normale Supérieure, Institut de Biologie de l'Ecole Normale Superieure (IBENS), CNRS, Inserm, Ecole Normale Supérieure, Paris Sciences et Lettres (PSL) Research University, F-75005 Paris, France; Programme Equipe Labellisées, Ligue Contre le Cancer, 75013 Paris, France; sweiss@chem.ucla.edu strick@biologie.ens.fr taatjes@colorado.edu.
Dylan J TaatjesDepartment of Chemistry & Biochemistry, University of Colorado, Boulder, CO 80309; sweiss@chem.ucla.edu strick@biologie.ens.fr taatjes@colorado.edu.
Shimon WeissDepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095; Molecular Biology Institute, University of California, Los Angeles, CA 90095; Department of Physiology, University of California, Los Angeles, CA 90095 sweiss@chem.ucla.edu strick@biologie.ens.fr taatjes@colorado.edu.
University of California, Los Angeles · USCentre National de la Recherche Scientifique · FRRowan University · USUniversity of Colorado Boulder · US

Funding

TRAINING IN SIGNAL TRANSDUCTION &CELL CYCLE REGULATIONT32GM008759 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI AHN, NATALIE G. · 2000 to 2020
$5.9M
Predoctoral Training Program in Signaling and Cellular Regulation INCLUDE Down Syndrome SupplementT32GM142607 · NIGMS · UNIVERSITY OF COLORADO · PI Sabrina Leigh Spencer, Tin Tin Su · 2021 to 2026
$3.6M
Single Molecule Studies of Prokaryotic and Eukaryotic Transcription MachineriesR01GM069709 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WEISS, SHIMON · 2005 to 2012
$2.9M
Single-photon counting APD arrays for high-through-put single-molecule assaysR01GM095904 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GHIONI, MASSIMO ANTONIO, MICHALET, XAVIER · 2012 to 2016
$2.0M
NIGMS NIH HHS R01 GM069709NIGMS NIH HHS R01 GM095904NIGMS NIH HHS T32 GM008759NIGMS NIH HHS T32 GM142607
6 · The paper itself

Abstract

Initiation is a highly regulated, rate-limiting step in transcription. We used a series of approaches to examine the kinetics of RNA polymerase (RNAP) transcription initiation in greater detail. Quenched kinetics assays, in combination with gel-based assays, showed that RNAP exit kinetics from complexes stalled at later stages of initiation (e.g., from a 7-base transcript) were markedly slower than from earlier stages (e.g., from a 2- or 4-base transcript). In addition, the RNAP-GreA endonuclease accelerated transcription kinetics from otherwise delayed initiation states. Further examination with magnetic tweezers transcription experiments showed that RNAP adopted a long-lived backtracked state during initiation and that the paused-backtracked initiation intermediate was populated abundantly at physiologically relevant nucleoside triphosphate (NTP) concentrations. The paused intermediate population was further increased when the NTP concentration was decreased and/or when an imbalance in NTP concentration was introduced (situations that mimic stress). Our results confirm the existence of a previously hypothesized paused and backtracked RNAP initiation intermediate and suggest it is biologically relevant; furthermore, such intermediates could be exploited for therapeutic purposes and may reflect a conserved state among paused, initiating eukaryotic RNA polymerase II enzymes.

Indexed as

Gene Expression Regulation, BacterialTranscription Initiation, GeneticBase SequenceEscherichia coliEscherichia coli ProteinsGuanosine TriphosphateKineticsNucleic Acid ConformationRNA, MessengerRNA Polymerase IISequence AlignmentTranscription FactorsUridine TriphosphateEscherichia coli ProteinsGreA protein, E coliGuanosine TriphosphateRNA, MessengerRNA Polymerase IITranscription FactorsUridine TriphosphatebacktrackingpausingRNAPRNA polymerasetranscription

Identifiers

PMID27729537
PMCPMC5087071
OpenAlexW2530360930

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.