Evidence map›Paper›PMID 25394904›Full record

ArticleBMC systems biology2014

Evolution of context dependent regulation by expansion of feast/famine regulatory proteins.

Christopher L Plaisier, Fang-Yin Lo, Justin Ashworth, Aaron N Brooks, Karlyn D Beer, Amardeep Kaur, Min Pan, David J Reiss, Marc T Facciotti, Nitin S Baliga

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Analysis ofGenes · 2021
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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

10 authors at 2 institutions in 1 country.

Christopher L PlaisierInstitute for Systems Biology, Seattle, WA, USA. cplaisier@systemsbiology.org.
Fang-Yin LoInstitute for Systems Biology, Seattle, WA, USA. fylo@systemsbiology.org.
Justin AshworthInstitute for Systems Biology, Seattle, WA, USA. justin.ashworth@systemsbiology.org.
Aaron N BrooksInstitute for Systems Biology, Seattle, WA, USA. abrooks@systemsbiology.org.
Karlyn D BeerInstitute for Systems Biology, Seattle, WA, USA. kbeer@systemsbiology.org.
Amardeep KaurInstitute for Systems Biology, Seattle, WA, USA. amardeep.kaur@systemsbiology.org.
Min PanInstitute for Systems Biology, Seattle, WA, USA. min.pan@systemsbiology.org.
David J ReissInstitute for Systems Biology, Seattle, WA, USA. david.reiss@systemsbiology.org.
Marc T FacciottiDepartment of Biomedical Engineering, University of California, Davis, CA, USA. mtfacciotti@ucdavis.edu.
Nitin S BaligaInstitute for Systems Biology, Seattle, WA, USA. nitin.baliga@systemsbiology.org.
Institute for Systems Biology · USUniversity of California, Davis · US

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
Interrogation of systems level mechanisms controlling DNA repair processesR01GM077398 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2007 to 2010
$1.3M
NIGMS NIH HHS 1R01GM077398-01A2NIGMS NIH HHS 2P50GM076547NIGMS NIH HHS P50 GM076547NIGMS NIH HHS R01 GM077398
6 · The paper itself

Abstract

backgroundExpansion of transcription factors is believed to have played a crucial role in evolution of all organisms by enabling them to deal with dynamic environments and colonize new environments. We investigated how the expansion of the Feast/Famine Regulatory Protein (FFRP) or Lrp-like proteins into an eight-member family in Halobacterium salinarum NRC-1 has aided in niche-adaptation of this archaeon to a complex and dynamically changing hypersaline environment.

resultsWe mapped genome-wide binding locations for all eight FFRPs, investigated their preference for binding different effector molecules, and identified the contexts in which they act by analyzing transcriptional responses across 35 growth conditions that mimic different environmental and nutritional conditions this organism is likely to encounter in the wild. Integrative analysis of these data constructed an FFRP regulatory network with conditionally active states that reveal how interrelated variations in DNA-binding domains, effector-molecule preferences, and binding sites in target gene promoters have tuned the functions of each FFRP to the environments in which they act. We demonstrate how conditional regulation of similar genes by two FFRPs, AsnC (an activator) and VNG1237C (a repressor), have striking environment-specific fitness consequences for oxidative stress management and growth, respectively.

conclusionsThis study provides a systems perspective into the evolutionary process by which gene duplication within a transcription factor family contributes to environment-specific adaptation of an organism.

Indexed as

Biological EvolutionEnvironmentAdaptation, BiologicalBinding SitesGene DuplicationGene Expression Regulation, ArchaealHalobacterium salinarumParaquatTranscription FactorsParaquatTranscription Factors

Identifiers

PMID25394904
PMCPMC4236453
OpenAlexW2156633632

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.