Evidence map›Paper›PMID 25274566›Full record

ArticleGenome biology and evolution2014

Evolution and functional implications of the tricarboxylic acid cycle as revealed by phylogenetic analysis.

João Henrique Frota Cavalcanti, Alberto A Esteves-Ferreira, Carla G S Quinhones, Italo A Pereira-Lima, Adriano Nunes-Nesi, Alisdair R Fernie, Wagner L Araújo

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 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

44 citing papers in PubMed, 90 citations in OpenAlex.

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  17. Physiological and Molecular Aspects of TwoBiotech (Basel (Switzerland)) · 2022
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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 2 institutions in 2 countries.

João Henrique Frota CavalcantiDepartamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil Max-Planck-Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil.
Alberto A Esteves-FerreiraDepartamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil Max-Planck-Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil.
Carla G S QuinhonesDepartamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil Max-Planck-Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil.
Italo A Pereira-LimaDepartamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil Max-Planck-Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil.
Adriano Nunes-NesiDepartamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil Max-Planck-Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil.
Alisdair R FernieMax-Planck-Institut für Molekulare Pflanzenphysiologie, Potsdam-Golm, Germany.
Wagner L AraújoDepartamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil Max-Planck-Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, MG, Brazil wlaraujo@ufv.br.
Universidade Federal de Viçosa · BRMax Planck Institute of Molecular Plant Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tricarboxylic acid (TCA) cycle, a crucial component of respiratory metabolism, is composed of a set of eight enzymes present in the mitochondrial matrix. However, most of the TCA cycle enzymes are encoded in the nucleus in higher eukaryotes. In addition, evidence has accumulated demonstrating that nuclear genes were acquired from the mitochondrial genome during the course of evolution. For this reason, we here analyzed the evolutionary history of all TCA cycle enzymes in attempt to better understand the origin of these nuclear-encoded proteins. Our results indicate that prior to endosymbiotic events the TCA cycle seemed to operate only as isolated steps in both the host (eubacterial cell) and mitochondria (alphaproteobacteria). The origin of isoforms present in different cell compartments might be associated either with gene-transfer events which did not result in proper targeting of the protein to mitochondrion or with duplication events. Further in silico analyses allow us to suggest new insights into the possible roles of TCA cycle enzymes in different tissues. Finally, we performed coexpression analysis using mitochondrial TCA cycle genes revealing close connections among these genes most likely related to the higher efficiency of oxidative phosphorylation in this specialized organelle. Moreover, these analyses allowed us to identify further candidate genes which might be used for metabolic engineering purposes given the importance of the TCA cycle during development and/or stress situations.

Indexed as

Biological EvolutionCitric Acid CycleMitochondriaPhylogenyPlant ProteinsPlant Proteinsmitochondriapathway evolutionphylogenyplant respirationTCA cycle

Identifiers

PMID25274566
PMCPMC4224347
OpenAlexW2165036371

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.