# Multicondition expression profiling reveals limitations of canonical housekeeping genes

**Authors:** Elias Projahn, Michael Walter, Georg Fuellen, Steffen Möller

PMC · DOI: 10.1186/s12864-026-12563-8 · BMC Genomics · 2026-01-27

## TL;DR

This paper introduces a new method to evaluate housekeeping genes, showing that many commonly used ones are affected by drugs, which challenges their reliability as reference genes.

## Contribution

A novel algorithm scores genes based on expression ubiquity, revealing limitations of traditional housekeeping genes under drug treatments.

## Key findings

- Many traditional housekeeping genes are strongly influenced by commonly used drugs.
- Some genes maintain strong invariance under chemical stimuli, making them better reference genes.
- An interactive web interface helps researchers select robust reference genes and explore gene rankings.

## Abstract

Housekeeping genes are commonly used as reference genes for analyzing expression data. We introduce an algorithm that scores and ranks genes based on their expression ubiquity using three criteria: the proportion of samples with high expression, overall expression levels, and expression invariance. The resulting continuous and configurable measure of gene ubiquity overcomes the limitations of current categorical classifications.

Using this measure, we systematically evaluate how genes traditionally assumed to be ubiquitously expressed (so-called stable housekeeping genes) respond to drugs. By integrating expression data from the Genotype-Tissue Expression portal (physiological conditions) and the Connectivity Map (drug effects), we identify subsets of genes that maintain strong invariance under chemical stimuli, rendering them particularly suitable as reference genes. At the same time, we show that many seemingly ubiquitous genes are strongly influenced by commonly used drugs. Our findings open up new conceptual perspectives on drug mechanisms and cellular regulatory responses and they call into question the reliability of several classic housekeeping genes.

To facilitate broader application of these results, we present an interactive web interface (https://ubigen.uni-rostock.de) that allows researchers to explore gene rankings, adjust scoring criteria and analyze specific gene sets. This platform facilitates the selection of robust, ubiquitously expressed reference genes for experimental applications and deepens our understanding of transcriptional regulation under physiological and chemically perturbed conditions.

The online version contains supplementary material available at 10.1186/s12864-026-12563-8.

## Full-text entities

- **Genes:** PPIA (peptidylprolyl isomerase A) [NCBI Gene 5478] {aka CYPA, CYPH, HEL-S-69p}, LDHA (lactate dehydrogenase A) [NCBI Gene 3939] {aka GSD11, HEL-S-133P, LDHM, PIG19}, HPRT1 (hypoxanthine phosphoribosyltransferase 1) [NCBI Gene 3251] {aka HGPRT, HPRT}, CST7 (cystatin F) [NCBI Gene 8530] {aka CMAP}, VIM (vimentin) [NCBI Gene 7431], B2M (beta-2-microglobulin) [NCBI Gene 567] {aka AMYLD6, IMD43, MHC1D4}, ALDOA (aldolase, fructose-bisphosphate A) [NCBI Gene 226] {aka ALDA, GSD12, HEL-S-87p}, PGK1 (phosphoglycerate kinase 1) [NCBI Gene 5230] {aka HEL-S-68p, MIG10, PGKA}, RPS18 (ribosomal protein S18) [NCBI Gene 6222] {aka D6S218E, HKE3, KE-3, KE3, S18, uS13}, TFRC (transferrin receptor) [NCBI Gene 7037] {aka CD71, IMD46, T9, TFR, TFR1, TR}, PGAM1 (phosphoglycerate mutase 1) [NCBI Gene 5223] {aka HEL-S-35, PGAM-B, PGAMA}, HMBS (hydroxymethylbilane synthase) [NCBI Gene 3145] {aka ENCEP, LENCEP, PBG-D, PBGD, PORC, UPS}, PFKP (phosphofructokinase, platelet) [NCBI Gene 5214] {aka ATP-PFK, PFK-C, PFK-P, PFKF}, ACTB (actin beta) [NCBI Gene 60] {aka BKRNS, BNS, BRWS1, CSMH, DDS1, PS1TP5BP1}, YWHAZ (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta) [NCBI Gene 7534] {aka 14-3-3-zeta, HEL-S-3, HEL-S-93, HEL4, KCIP-1, POPCHAS}, GUSB (glucuronidase beta) [NCBI Gene 2990] {aka BG, MPS7}, IPO8 (importin 8) [NCBI Gene 10526] {aka RANBP8, VISS}, G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539] {aka CNSHA1, G6PD1}, ATP5F1B (ATP synthase F1 subunit beta) [NCBI Gene 506] {aka ATP5B, ATPMB, ATPSB, DYT38, HEL-S-271, HUMOP2}, TBP (TATA-box binding protein) [NCBI Gene 6908] {aka GTF2D, GTF2D1, HDL4, SCA17, TBP1, TFIID}
- **Diseases:** Glioma (MESH:D005910), Cancer (MESH:D009369), hypoxia (MESH:D000860), GTEx (MESH:D001039), toxicities (MESH:D064420), HPA (MESH:C483996)
- **Chemicals:** piperacillin (MESH:D010878), phenylpropanolamine (MESH:D010665), paroxetine (MESH:D017374), iron (MESH:D007501), trihexyphenidyl (MESH:D014282), benfluorex (MESH:C001584), nialamide (MESH:D009526), josamycin (MESH:D015570), proguanil (MESH:D002727), amikacin (MESH:D000583), serotonin (MESH:D012701), pindolol (MESH:D010869)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12918141/full.md

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Source: https://tomesphere.com/paper/PMC12918141