Evidence map›Paper›PMID 29388765›Full record

ArticleBiochemistry2019

Systematic Dissection of Sequence Elements Controlling σ70 Promoters Using a Genomically Encoded Multiplexed Reporter Assay in Escherichia coli.

Guillaume Urtecho, Arielle D Tripp, Kimberly D Insigne, Hwangbeom Kim, Sriram Kosuri

Open access · greenAbstract read
In one paragraph

Article in Biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
8.1field-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

58 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Comparative Characterization of σInternational journal of molecular sciences · 2026
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  7. PoolParty: streamlined design of DNA sequence libraries in Python.bioRxiv : the preprint server for biology · 2026
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  10. The Environment-Dependent Regulatory Landscape of thebioRxiv : the preprint server for biology · 2025
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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

5 authors at 1 institution in 1 country.

Guillaume UrtechoMolecular Biology Interdepartmental Doctoral Program , University of California , Los Angeles , California 90095 , United States.
Arielle D TrippDepartment of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , California 90095 , United States.
Kimberly D InsigneBioinformatics Interdepartmental Graduate Program , University of California , Los Angeles , California 90095 , United States.
Hwangbeom KimDepartment of Chemistry and Biochemistry , University of California , Los Angeles , California 90095 , United States.
Sriram KosuriDepartment of Chemistry and Biochemistry , University of California , Los Angeles , California 90095 , United States.ORCID 0000-0002-4661-0600
University of California, Los Angeles · US

Funding

UCLA MSD ProgramR25GM055052 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BARBER, PAUL HENRY, HASSON, TAMA W. · 1996 to 2021
$9.2M
LOS ANGELES BASIN BRIDGES TO THE PHD PROGRAMR25GM054939 · NIGMS · CALIFORNIA STATE UNIVERSITY LOS ANGELES · PI DRAKE REITAN, MEREDITH, GUTIERREZ, CARLOS GABRIEL · 1996 to 2020
$3.4M
REVERSE GENOMICS OF REGULATORY ELEMENTS GOVERNING SPLICINGDP2GM114829 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KOSURI, SRIRAM · 2014 to 2014
$2.3M
MOLECULAR DISSECTION OF MYOSIN VIIAR01EY012695 · NEI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI HASSON, TAMA W · 2001 to 2004
$1.1M
NIGMS NIH HHS DP2 GM114829NIGMS NIH HHS R25 GM055052
6 · The paper itself

Abstract

Promoters are the key drivers of gene expression and are largely responsible for the regulation of cellular responses to time and environment. In Escherichia coli, decades of studies have revealed most, if not all, of the sequence elements necessary to encode promoter function. Despite our knowledge of these motifs, it is still not possible to predict the strength and regulation of a promoter from primary sequence alone. Here we develop a novel multiplexed assay to study promoter function in E. coli by building a site-specific genomic recombination-mediated cassette exchange system that allows for the facile construction and testing of large libraries of genetic designs integrated into precise genomic locations. We build and test a library of 10898 σ70 promoter variants consisting of all combinations of a set of eight -35 elements, eight -10 elements, three UP elements, eight spacers, and eight backgrounds. We find that the -35 and -10 sequence elements can explain approximately 74% of the variance in promoter strength within our data set using a simple log-linear statistical model. Simple neural network models explain >95% of the variance in our data set by capturing nonlinear interactions with the spacer, background, and UP elements.

Indexed as

Base SequenceDNA-Directed RNA PolymerasesEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialGene LibraryGenomicsNerve NetPromoter Regions, GeneticProtein BindingSigma FactorTranscription, GeneticDNA-Directed RNA PolymerasesEscherichia coli ProteinsSigma Factor

Identifiers

PMID29388765
PMCPMC6389444
OpenAlexW2766831674

What OpenQuestion holds

Textmetadata
LicenceTDM
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.