Evidence map›Paper›PMID 32101716›Full record

ArticleBiophysical journal2020

Probing Mechanisms of Transcription Elongation Through Cell-to-Cell Variability of RNA Polymerase.

Md Zulfikar Ali, Sandeep Choubey, Dipjyoti Das, Robert C Brewster

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

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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

4 authors at 3 institutions in 3 countries.

Md Zulfikar AliProgram in Systems Biology, University of Massachusetts Medical School, Worcester, Massachusetts; Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts.
Sandeep ChoubeyMax Planck institute for the Physics of Complex Systems, Dresden, Germany. Electronic address: sandeep@pks.mpg.de.
Dipjyoti DasDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Nadia, West Bengal, India.
Robert C BrewsterProgram in Systems Biology, University of Massachusetts Medical School, Worcester, Massachusetts; Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts. Electronic address: robert.brewster@umassmed.edu.
University of Massachusetts Chan Medical School · USIndian Institute of Science Education and Research Kolkata · INMax Planck Institute for the Physics of Complex Systems · DE

Funding

Uncovering the fundamental principles of transcriptional regulationR35GM128797 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREWSTER, ROBERT CHARLES · 2018 to 2022
$2.1M
NIGMS NIH HHS R35 GM128797
6 · The paper itself

Abstract

The process of transcription initiation and elongation are primary points of control in the regulation of gene expression. Although biochemical studies have uncovered the mechanisms involved in controlling transcription at each step, how these mechanisms manifest in vivo at the level of individual genes is still unclear. Recent experimental advances have enabled single-cell measurements of RNA polymerase (RNAP) molecules engaged in the process of transcribing a gene of interest. In this article, we use Gillespie simulations to show that measurements of cell-to-cell variability of RNAP numbers and interpolymerase distances can reveal the prevailing mode of regulation of a given gene. Mechanisms of regulation at each step, from initiation to elongation dynamics, produce qualitatively distinct signatures, which can further be used to discern between them. Most intriguingly, depending on the initiation kinetics, stochastic elongation can either enhance or suppress cell-to-cell variability at the RNAP level. To demonstrate the value of this framework, we analyze RNAP number distribution data for ribosomal genes in Saccharomyces cerevisiae from three previously published studies and show that this approach provides crucial mechanistic insights into the transcriptional regulation of these genes.

Indexed as

Escherichia coliTranscription, GeneticDNA-Directed RNA PolymerasesGene Expression RegulationKineticsDNA-Directed RNA Polymerases

Identifiers

PMID32101716
PMCPMC7136280
OpenAlexW3006642818

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.