Evidence map›Paper›PMID 25552531›Full record

ArticleGenome biology and evolution2014

Extreme features of the Galdieria sulphuraria organellar genomes: a consequence of polyextremophily?

Kanika Jain, Kirsten Krause, Felix Grewe, Gaven F Nelson, Andreas P M Weber, Alan C Christensen, Jeffrey P Mower

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-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

15 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Discovery of Conserved and Novel MicroRNAs inIranian journal of biotechnology · 2021
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  7. Review
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  11. Evolutionary Dynamics of Cryptophyte Plastid Genomes.Genome biology and evolution · 2017
    Article
  12. Article
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  15. Article
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

7 authors at 3 institutions in 3 countries.

Kanika JainCenter for Plant Science Innovation, University of Nebraska - Lincoln School of Biological Sciences, University of Nebraska - Lincoln.
Kirsten KrauseDepartment of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway.
Felix GreweCenter for Plant Science Innovation, University of Nebraska - Lincoln Department of Agronomy and Horticulture, University of Nebraska - Lincoln.
Gaven F NelsonCenter for Plant Science Innovation, University of Nebraska - Lincoln School of Biological Sciences, University of Nebraska - Lincoln.
Andreas P M WeberInstitute of Plant Biochemistry, Cluster of Excellence on Plant Science, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Alan C ChristensenSchool of Biological Sciences, University of Nebraska - Lincoln.
Jeffrey P MowerCenter for Plant Science Innovation, University of Nebraska - Lincoln Department of Agronomy and Horticulture, University of Nebraska - Lincoln jpmower@unl.edu.
University of Nebraska–Lincoln · USCluster of Excellence on Plant Sciences · DEUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear genome sequencing from extremophilic eukaryotes has revealed clues about the mechanisms of adaptation to extreme environments, but the functional consequences of extremophily on organellar genomes are unknown. To address this issue, we assembled the mitochondrial and plastid genomes from a polyextremophilic red alga, Galdieria sulphuraria strain 074 W, and performed a comparative genomic analysis with other red algae and more broadly across eukaryotes. The mitogenome is highly reduced in size and genetic content and exhibits the highest guanine-cytosine skew of any known genome and the fastest substitution rate among all red algae. The plastid genome contains a large number of intergenic stem-loop structures but is otherwise rather typical in size, structure, and content in comparison with other red algae. We suggest that these unique genomic modifications result not only from the harsh conditions in which Galdieria lives but also from its unusual capability to grow heterotrophically, endolithically, and in the dark. These conditions place additional mutational pressures on the mitogenome due to the increased reliance on the mitochondrion for energy production, whereas the decreased reliance on photosynthesis and the presence of numerous stem-loop structures may shield the plastome from similar genomic stress.

Indexed as

Amino Acid SequenceBase SequenceEukaryotaGenome, MitochondrialGenome, PlastidGenomicsOrganellesPhotosynthesisPlant ProteinsPlastidsRhodophytaSequence Homology, Amino AcidPlant Proteinsfacultative heterotrophyGaldieria sulphurariaGC skewpolyextremophilyred algaesubstitution rate

Identifiers

PMID25552531
PMCPMC4316638
OpenAlexW2167498777

What OpenQuestion holds

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LicenceCC BY-NC
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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.