Evidence map›Paper›PMID 25393412›Full record

ArticlePLoS genetics2014

Phylogenetically driven sequencing of extremely halophilic archaea reveals strategies for static and dynamic osmo-response.

Erin A Becker, Phillip M Seitzer, Andrew Tritt, David Larsen, Megan Krusor, Andrew I Yao, Dongying Wu, Dominique Madern, Jonathan A Eisen, Aaron E Darling and 1 more

Abstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
–field-weighted citation impact
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

82 citing papers in PubMed.

  1. Article
  2. Irrigation ofMicroorganisms · 2025
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  6. Determination ofJournal of the Royal Society, Interface · 2025
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22 more citing papers are in PubMed but not listed here.

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

11 authors.

Erin A BeckerMicrobiology Graduate Group, University of California, Davis, Davis, California, United States of America; Genome Center, University of California, Davis, Davis, California, United States of America.
Phillip M SeitzerGenome Center, University of California, Davis, Davis, California, United States of America; Department of Biomedical Engineering, University of California, Davis, Davis, California, United States of America; Proteome Software, Portland, Oregon, United States of America.
Andrew TrittDepartment of Energy Joint Genomes Institute, Walnut Creek, California, United States of America.
David LarsenGenome Center, University of California, Davis, Davis, California, United States of America.
Megan KrusorMicrobiology Graduate Group, University of California, Davis, Davis, California, United States of America; Department of Earth and Planetary Sciences, University of California, Davis, Davis, California, United States of America.
Andrew I YaoGenome Center, University of California, Davis, Davis, California, United States of America; Department of Biomedical Engineering, University of California, Davis, Davis, California, United States of America.
Dongying WuDepartment of Energy Joint Genomes Institute, Walnut Creek, California, United States of America.
Dominique MadernUniversité Grenoble Alpes, Institut de Biologie Structurale, Grenoble, France; Centre National de la Recherche Scientifique, Institut de Biologie Structurale, Grenoble, France; Commissariat à l'énergie Atomique et aux Énergies Alternatives, Département du Science du Vivant, Institut de Biologie Structurale, Grenoble, France.
Jonathan A EisenMicrobiology Graduate Group, University of California, Davis, Davis, California, United States of America; Genome Center, University of California, Davis, Davis, California, United States of America.
Aaron E Darlingithree Institute, University of Technology, Sydney, Australia.
Marc T FacciottiMicrobiology Graduate Group, University of California, Davis, Davis, California, United States of America; Genome Center, University of California, Davis, Davis, California, United States of America; Department of Biomedical Engineering, University of California, Davis, Davis, California, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organisms across the tree of life use a variety of mechanisms to respond to stress-inducing fluctuations in osmotic conditions. Cellular response mechanisms and phenotypes associated with osmoadaptation also play important roles in bacterial virulence, human health, agricultural production and many other biological systems. To improve understanding of osmoadaptive strategies, we have generated 59 high-quality draft genomes for the haloarchaea (a euryarchaeal clade whose members thrive in hypersaline environments and routinely experience drastic changes in environmental salinity) and analyzed these new genomes in combination with those from 21 previously sequenced haloarchaeal isolates. We propose a generalized model for haloarchaeal management of cytoplasmic osmolarity in response to osmotic shifts, where potassium accumulation and sodium expulsion during osmotic upshock are accomplished via secondary transport using the proton gradient as an energy source, and potassium loss during downshock is via a combination of secondary transport and non-specific ion loss through mechanosensitive channels. We also propose new mechanisms for magnesium and chloride accumulation. We describe the expansion and differentiation of haloarchaeal general transcription factor families, including two novel expansions of the TATA-binding protein family, and discuss their potential for enabling rapid adaptation to environmental fluxes. We challenge a recent high-profile proposal regarding the evolutionary origins of the haloarchaea by showing that inclusion of additional genomes significantly reduces support for a proposed large-scale horizontal gene transfer into the ancestral haloarchaeon from the bacterial domain. The combination of broad (17 genera) and deep (≥5 species in four genera) sampling of a phenotypically unified clade has enabled us to uncover both highly conserved and specialized features of osmoadaptation. Finally, we demonstrate the broad utility of such datasets, for metagenomics, improvements to automated gene annotation and investigations of evolutionary processes.

Indexed as

MetagenomicsAdaptation, PhysiologicalArchaeaBase SequenceEvolution, MolecularGenome, ArchaealHumansMolecular Sequence AnnotationOsmolar ConcentrationPhylogenySalinityTATA-Box Binding ProteinTATA-Box Binding Protein

Identifiers

PMID25393412
PMCPMC4230888

What OpenQuestion holds

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Registered trials

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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.