Evidence map›Paper›PMID 31229574›Full record

ArticleMitochondrion2019

Do angiosperms with highly divergent mitochondrial genomes have altered mitochondrial function?

Justin C Havird, Gregory R Noe, Luke Link, Amber Torres, David C Logan, Daniel B Sloan, Adam J Chicco

Open access · greenAbstract read
In one paragraph

Article in Mitochondrion, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  5. Genome copy number predicts extreme evolutionary rate variation in plant mitochondrial DNA.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

7 authors at 3 institutions in 2 countries.

Justin C HavirdDepartment of Biology, Colorado State University, Fort Collins, CO, USA; Department of Integrative Biology, The University of Texas, Austin, TX, USA. Electronic address: jhavird@utexas.edu.
Gregory R NoeDepartment of Biology, Colorado State University, Fort Collins, CO, USA.
Luke LinkDepartment of Biology, Colorado State University, Fort Collins, CO, USA.
Amber TorresDepartment of Biology, Colorado State University, Fort Collins, CO, USA. Electronic address: marikat@rams.colostate.edu.
David C LoganIRHS, INRA, Université d'Angers, AGROCAMPUS-Ouest, SFR 4207 QUASAV, 49071 Beaucouzé cedex, France.
Daniel B SloanDepartment of Biology, Colorado State University, Fort Collins, CO, USA. Electronic address: dbsloan@rams.colostate.edu.
Adam J ChiccoDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO, USA. Electronic address: Adam.Chicco@colostate.edu.
Colorado State University · USThe University of Texas at Austin · USUniversité d'Angers · FR

Funding

Supplement request for 1F32GM116361-01F32GM116361 · NIGMS · COLORADO STATE UNIVERSITY · PI HAVIRD, JUSTIN C · 2015 to 2017
$168k
NIGMS NIH HHS F32 GM116361
6 · The paper itself

Abstract

Angiosperm mitochondrial (mt) genes are generally slow-evolving, but multiple lineages have undergone dramatic accelerations in rates of nucleotide substitution and extreme changes in mt genome structure. While molecular evolution in these lineages has been investigated, very little is known about their mt function. Some studies have suggested altered respiration in individual taxa, although there are several reasons why mt variation might be neutral in others. Here, we develop a new protocol to characterize respiration in isolated plant mitochondria and apply it to species of Silene with mt genomes that are rapidly evolving, highly fragmented, and exceptionally large (~11 Mbp). This protocol, complemented with traditional measures of plant fitness, cytochrome c oxidase activity assays, and fluorescence microscopy, was also used to characterize inter- and intraspecific variation in mt function. Contributions of the individual "classic" OXPHOS complexes, the alternative oxidase, and external NADH dehydrogenases to overall mt respiratory flux were found to be similar to previously studied angiosperms with more typical mt genomes. Some differences in mt function could be explained by inter- and intraspecific variation. This study suggests that Silene species with peculiar mt genomes still show relatively normal mt respiration. This may be due to strong purifying selection on mt variants, coevolutionary responses in the nucleus, or a combination of both. Future experiments should explore such questions using a comparative framework and investigating other lineages with unusual mitogenomes.

Indexed as

Genome, MitochondrialGenome, PlantSileneAlternative NADH dehydrogenaseCytonuclear interactionsFlux control factorMitochondrial respirationOroboros Oxygraph 2KSUIT protocol

Identifiers

PMID31229574
PMCPMC6885534
OpenAlexW2952471918

What OpenQuestion holds

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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.