Evidence map›Paper›PMID 42290180›Full record

ArticleBiology open2026

Retention and tissue-specific expression of uncoupling protein homoeologs in Xenopus laevis.

Erik Rollwitz, Martin Jastroch

Abstract read
In one paragraph

Article in Biology open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Erik RollwitzDepartment of Molecular Biosciences, The Wenner-Gren Institute (MBW), Stockholm University, SE-106 91 Stockholm, Sweden.
Martin JastrochDepartment of Molecular Biosciences, The Wenner-Gren Institute (MBW), Stockholm University, SE-106 91 Stockholm, Sweden.ORCID 0000-0003-0358-3865

Funding

Stockholm UniversitySwedish Research Council 2022-03136Vetenskapsradet Grant No 2022-03136
6 · The paper itself

Abstract

Mitochondrial uncoupling proteins (UCPs) play central roles in vertebrate energy metabolism, with UCP1 specializing as a thermogenic effector in placental mammals. Comparative genomics demonstrated that UCP1, UCP2, and UCP3 originated prior to the emergence of endothermy, suggesting that their ancestral functions evolved in ectothermic vertebrates. Here, we investigated the genomic organization, conserved synteny, and mRNA expression of all three UCP paralogs and homoeologs in the allotetraploid amphibian Xenopus laevis. Comparative genome analyses revealed that all three UCP paralogs and their long (L) and short (S) homoeologs were retained following polyploidization, although local rearrangements were evident for neighboring genes at the UCP2/UCP3 locus. Quantitative expression analyses across adult frog tissues revealed pronounced tissue specificity, with predominant expression of UCP1 and UCP2 in kidney, UCP3 in muscle, and differences in UCP2 homoeolog expression levels. Together, these findings establish a framework for UCPs in an amphibian model organism, primarily linking them to energetically demanding tissues.

Indexed as

Gene Expression RegulationMitochondrial Uncoupling ProteinsXenopus laevisXenopus ProteinsAnimalsEvolution, MolecularGene Expression ProfilingGenomicsOrgan SpecificityPhylogenySyntenyMitochondrial Uncoupling ProteinsXenopus ProteinsAmphibiansHomoeologsUncoupling proteins

Identifiers

PMID42290180
PMCPMC13382700

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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.