Evidence map›Paper›PMID 40577420›Full record

ArticlePLoS genetics2025

Functional analysis of CYP4B1 enzymes from apes and humans uncovers evolutionary hot spots for adaptations of the catalytical function.

Saskia Hüsken, Annika Röder, Johannes Ptok, Anne E Meyer, Mats Georg, Yannick Schwarz, Christian Roos, Kerstin Mätz-Rensing, Michael C Hutter, Doreen M Floss and 4 more

Abstract read
In one paragraph

Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

14 authors.

Saskia HüskenDepartment of Otorhinolaryngology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0000-0002-7947-3315
Annika RöderInstitute of Biochemistry, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0009-0003-3644-4041
Johannes PtokInstitute of Virology, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0000-0002-0322-5649
Anne E MeyerDepartment of Otorhinolaryngology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.
Mats GeorgInstitute of Organic Chemistry, Justus Liebig University Giessen, Giessen, Germany.ORCID https://orcid.org/0009-0006-4631-2853
Yannick SchwarzDepartment of Otorhinolaryngology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0009-0005-5559-7582
Christian RoosGerman Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.ORCID https://orcid.org/0000-0003-0190-4266
Kerstin Mätz-RensingGerman Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Michael C HutterCenter for Bioinformatics, Saarland University, Saarbrücken, Germany.ORCID https://orcid.org/0000-0003-3168-6554
Doreen M FlossMedical Faculty and University Hospital Düsseldorf, Institute of Biochemistry and Molecular Biology II, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0000-0002-6675-5313
Allan E RettieDepartment of Medicinal Chemistry, School of Pharmacy, University of Washington, Seattle, Washington, United States of America.
Marco GirhardInstitute of Biochemistry, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0000-0002-9054-3628
Helmut HanenbergDepartment of Otorhinolaryngology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.
Constanze WiekDepartment of Otorhinolaryngology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0000-0003-2214-8148

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A hallmark of the highly conserved CYP4B1 enzyme in mammals is the capability to bioactivate both xenobiotic and endobiotic substrates. However, due to a single amino acid change (p.P427S) within the evolutionary conserved meander region no catalytic activity of the native human CYP4B1 has been identified so far. To identify at which point in human evolution the loss of CYP4B1 activity had occurred, we evaluated the activities of CYP4B1 orthologs from 14 primate genera against 4-ipomeanol and perilla ketone in human liver cells. The activity of recombinant CYP4B1 proteins isolated from E. coli was also tested against 4-ipomeanol and lauric acid. Surprisingly, CYP4B1 already became catalytically inactive at the split between apes and monkeys; all tested CYP4B1 orthologs from monkeys were able to bioactivate both protoxins and to hydroxylate lauric acid. Amino acid analysis of the CYP4B1 orthologs revealed four additional evolutionary changes, each affecting the function of ape and human enzymes: p.V71G specific for Denisovans, p.R106C, p.R244H, and an exon deletion found only in the gorilla CYP4B1. Systematic functional analyses proved the negative impact of the genetic changes on CYP4B1 activity and showed that reversion of the mutations restored enzyme activity. The occurrence of five independent inactivating genetic changes in the same gene of closely related species is a clear indication of the importance of inactivating CYP4B1 in apes and humans. Elucidating the evolutionary trigger(s) for CYP4B1 inactivation in our ancestors will ultimately improve our understanding of primate evolution.

Indexed as

Cytochrome P-450 Enzyme SystemEvolution, MolecularHominidaeAmino Acid SequenceAmino Acid SubstitutionAnimalsAryl Hydrocarbon HydroxylasesHumansLauric AcidsPhylogenyAryl Hydrocarbon Hydroxylasescytochrome P-450 CYP4B1Cytochrome P-450 Enzyme Systemlauric acidLauric Acids

Identifiers

PMID40577420
PMCPMC12233900

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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.