Evidence map›Paper›PMID 35915220›Full record

ArticleScientific reports2022

The major urinary protein gene cluster knockout mouse as a novel model for translational metabolism research.

Sarah Greve, Gisela A Kuhn, Mara D Saenz-de-Juano, Adhideb Ghosh, Ferdinand von Meyenn, Katrin Giller

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Hepatocyte-SpecificAntioxidants (Basel, Switzerland) · 2026
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  5. Frontiers in immunology · 2026
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  12. Colonization withbioRxiv : the preprint server for biology · 2025
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  13. Sex-specific characterization of aortic function and inflammation in a new diet-induced mouse model of metabolic syndrome.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  14. Article
  15. Article
  16. Major urinary protein (Microbiology spectrum · 2024
    Article
  17. 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

6 authors at 1 institution in 1 country.

Sarah GreveAnimal Nutrition, ETH Zurich, Universitaetstrasse 2, 8092, Zurich, Switzerland.
Gisela A KuhnInstitute for Biomechanics, ETH Zurich, Leopold-Ruzicka-Weg 4, 8093, Zurich, Switzerland.
Mara D Saenz-de-JuanoAnimal Physiology, ETH Zurich, Universitaetstrasse 2, 8092, Zurich, Switzerland.
Adhideb GhoshLaboratory of Nutrition and Metabolic Epigenetics, ETH Zurich, Schorenstrasse 16, 8603, Schwerzenbach, Switzerland.
Ferdinand von MeyennLaboratory of Nutrition and Metabolic Epigenetics, ETH Zurich, Schorenstrasse 16, 8603, Schwerzenbach, Switzerland.
Katrin GillerAnimal Nutrition, ETH Zurich, Universitaetstrasse 2, 8092, Zurich, Switzerland. katrin.giller@usys.ethz.ch.
ETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scientific evidence suggests that not only murine scent communication is regulated by major urinary proteins, but that their expression may also vary in response to metabolism via a yet unknown mechanism. Major urinary proteins are expressed mainly in the liver, showing a sexually dimorphic pattern with substantially higher expression in males. Here, we investigate the metabolic implications of a major urinary protein knockout in twelve-week-old male and female C57BL/6N mice during ad libitum feeding. Despite both sexes of major urinary protein knockout mice displayed numerically increased body weight and visceral adipose tissue proportions compared to sex-matched wildtype mice, the main genotype-specific metabolic differences were observed exclusively in males. Male major urinary protein knockout mice exhibited plasma and hepatic lipid accumulation accompanied by a hepatic transcriptome indicating an activation of lipogenesis. These findings match the higher major urinary protein expression in male compared to female wildtype mice, suggesting a more distinct reduction in energy requirements in male compared to female major urinary protein knockout mice. The observed sex-specific anabolic phenotype confirms a role of major urinary protein in metabolism and, since major urinary proteins are not expressed in humans, suggests the major urinary protein knockout mouse as a potential alternative model for translational metabolism research which needs to be further elucidated.

Indexed as

LiverProteinsAnimalsFemaleHumansLipid MetabolismMaleMiceMice, Inbred C57BLMice, KnockoutMultigene Familymajor urinary proteinsProteins

Identifiers

PMID35915220
PMCPMC9343454
OpenAlexW4289203197

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.