# A housekeeping gene search to analyze expression changes of individual genes in Macaca mulatta

**Authors:** M.V. Shulskaya, A.Kh. Alieva, I.R. Kumakov, M.I. Shadrina, P.A. Slominsky

PMC · DOI: 10.18699/vjgb-25-138 · Vavilov Journal of Genetics and Breeding · 2025-12-01

## TL;DR

This paper identifies stable housekeeping genes in rhesus macaques for reliable gene expression analysis in the brain and blood.

## Contribution

The study provides two panels of candidate housekeeping genes for rhesus macaques, including 56 and 8 genes.

## Key findings

- Two panels of housekeeping genes were identified for M. mulatta.
- The genes are stably expressed in the brain and peripheral blood of rhesus macaques.
- The panels lack pseudogenes in macaques and humans.

## Abstract

Rhesus macaques (Macaca mulatta) are the most common non-human primates living in captivity. The use of rhesus macaques as model objects is determined, first of all, by their phylogenetic and physiological closeness to humans, and, as a consequence, the possibility of extrapolating the obtained results to humans. Currently, it is known that a number of biochemical changes occur under various physiological conditions, including at the transcriptomic level. The real-time polymerase chain reaction is a widely used universal method for gene expression analysis. Carrying out such studies always requires a preliminary selection of “housekeeping genes” (HKGs) – genes necessary for the implementation of basic functions in the cell and stably expressed in different cell types and under different conditions. At present, there are only two systematic studies on the search for HKGs in the rhesus macaque brain, and therefore in this work a search and systematization of HKGs for this species were carried out. As a result, two panels of promising HKGs for M. mulatta were formed: an extended panel, consisting of 56 genes, and a small panel, consisting of 8 genes: ARHGDIA, CYB5R1, NDUFA7, RRAGA, TTC1, UBA6, VPS72, and YWHAH. Both panels of potential HKGs do not have pseudogenes in macaques or humans, are characterized by stable and sufficient expression in the brain of rhesus macaques and can be used to analyze expression not only in the brain but also in peripheral blood. However, it should be noted that the data have not been experimentally verified and require verification in laboratory conditions.

## Linked entities

- **Genes:** ARHGDIA (Rho GDP dissociation inhibitor alpha) [NCBI Gene 396], CYB5R1 (cytochrome b5 reductase 1) [NCBI Gene 51706], NDUFA7 (NADH:ubiquinone oxidoreductase subunit A7) [NCBI Gene 4701], RRAGA (Ras related GTP binding A) [NCBI Gene 10670], TTC1 (tetratricopeptide repeat domain 1) [NCBI Gene 7265], UBA6 (ubiquitin like modifier activating enzyme 6) [NCBI Gene 55236], VPS72 (vacuolar protein sorting 72 homolog) [NCBI Gene 6944], YWHAH (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta) [NCBI Gene 7533]
- **Species:** Macaca mulatta (taxon 9544)

## Full-text entities

- **Genes:** MLH1 (mutL homolog 1) [NCBI Gene 698782], DIAPH1 (diaphanous related formin 1) [NCBI Gene 1729] {aka DFNA1, DIA1, DRF1, LFHL1, SCBMS, hDIA1}, NDUFA7 (NADH:ubiquinone oxidoreductase subunit A7) [NCBI Gene 711212], RPL37 (ribosomal protein L37) [NCBI Gene 6167] {aka L37, eL37}, TTC1 (tetratricopeptide repeat domain 1) [NCBI Gene 695225], JPH3 (junctophilin 3) [NCBI Gene 704611], RPGR (retinitis pigmentosa GTPase regulator) [NCBI Gene 714316], CYB5R1 (cytochrome b5 reductase 1) [NCBI Gene 704519], CSNK2B (casein kinase 2 beta) [NCBI Gene 1460] {aka CK II beta, CK2B, CK2N, CSK2B, Ckb1, Ckb2}, PRPF8 (pre-mRNA processing factor 8) [NCBI Gene 10594] {aka HPRP8, PRP8, PRPC8, RP13, SNRNP220}, LDHA (lactate dehydrogenase A) [NCBI Gene 3939] {aka GSD11, HEL-S-133P, LDHM, PIG19}, YWHAH (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta) [NCBI Gene 7533] {aka YWHA1}, TMED9 (transmembrane p24 trafficking protein 9) [NCBI Gene 54732] {aka GMP25, HSGP25L2G, p24a2, p24alpha2, p25}, VCP (valosin containing protein) [NCBI Gene 698707], MFSD8 (major facilitator superfamily domain containing 8) [NCBI Gene 256471] {aka CCMD, CLN7, SLC74A1}, RP1 [NCBI Gene 677695], RRAGA (Ras related GTP binding A) [NCBI Gene 10670] {aka FIP-1, FIP1, RAGA}, UBA6 (ubiquitin like modifier activating enzyme 6) [NCBI Gene 55236] {aka E1-L2, MOP-4, UBE1L2}, ARHGDIA (Rho GDP dissociation inhibitor alpha) [NCBI Gene 396] {aka GDIA1, HEL-S-47e, NPHS8, RHOGDI, RHOGDI-1}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 574353], B4GALT3 (beta-1,4-galactosyltransferase 3) [NCBI Gene 8703] {aka beta4Gal-T3}, TMED3 (transmembrane p24 trafficking protein 3) [NCBI Gene 711993], TBP (TATA-box binding protein) [NCBI Gene 6908] {aka GTF2D, GTF2D1, HDL4, SCA17, TBP1, TFIID}, CYB5R1 (cytochrome b5 reductase 1) [NCBI Gene 51706] {aka B5R.1, B5R1, B5R2, NQO3A2, humb5R2}, NDUFA1 (NADH:ubiquinone oxidoreductase subunit A1) [NCBI Gene 4694] {aka CI-MWFE, MC1DN12, MWFE, ZNF183}, TYRP1 (tyrosinase related protein 1) [NCBI Gene 714646], ACTB (actin beta) [NCBI Gene 574285], CNIH4 (cornichon family AMPA receptor auxiliary protein 4) [NCBI Gene 701767], UBB (ubiquitin B) [NCBI Gene 7314] {aka HEL-S-50}, AHSA1 (activator of HSP90 ATPase activity 1) [NCBI Gene 10598] {aka AHA1, C14orf3, hAha1, p38}, RRAGA (Ras related GTP binding A) [NCBI Gene 100430225], RAD23A (RAD23 nucleotide excision repair protein A) [NCBI Gene 5886] {aka HHR23A, HR23A}, RPS27A (ribosomal protein S27a) [NCBI Gene 6233] {aka CEP80, HEL112, S27A, UBA80, UBCEP1, UBCEP80}, HPCAL1 (hippocalcin like 1) [NCBI Gene 3241] {aka BDR1, HLP2, VILIP-3}, MAPKAPK2 (MAPK activated protein kinase 2) [NCBI Gene 9261] {aka MAPKAP-K2, MK-2, MK2}, SNRPA (small nuclear ribonucleoprotein polypeptide A) [NCBI Gene 6626] {aka Mud1, U1-A, U1A}, MIR27A (microRNA 27a) [NCBI Gene 407018] {aka MIR27, MIRN27A, mir-27a}, NDUFA7 (NADH:ubiquinone oxidoreductase subunit A7) [NCBI Gene 4701] {aka B14.5a, CI-B14.5a}, TTC1 (tetratricopeptide repeat domain 1) [NCBI Gene 7265] {aka TPR1}, UBA6 (ubiquitin like modifier activating enzyme 6) [NCBI Gene 711751], ARHGDIA (Rho GDP dissociation inhibitor alpha) [NCBI Gene 714752], LDHB (lactate dehydrogenase B) [NCBI Gene 3945] {aka HEL-S-281, LDH-B, LDH-H, LDHBD, TRG-5}, IRF2BPL (interferon regulatory factor 2 binding protein like) [NCBI Gene 704474] {aka C14orf4L, EAP1}, VPS72 (vacuolar protein sorting 72 homolog) [NCBI Gene 709818], MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, HSPA8 (heat shock protein family A (Hsp70) member 8) [NCBI Gene 707989], ARL2 (ARF like GTPase 2) [NCBI Gene 402] {aka ARFL2, MRCS1}, RPL19 (ribosomal protein L19) [NCBI Gene 6143] {aka L19, eL19}, SSR2 (signal sequence receptor subunit 2) [NCBI Gene 6746] {aka HSD25, TLAP, TRAP-BETA, TRAPB}, VPS72 (vacuolar protein sorting 72 homolog) [NCBI Gene 6944] {aka Swc2, TCFL1, YL-1, YL1}, Hspa8 (heat shock protein family A (Hsp70) member 8) [NCBI Gene 24468] {aka Hsc70}, TYR (tyrosinase) [NCBI Gene 705792], ATXN3 (ataxin 3) [NCBI Gene 720515], YWHAH (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta) [NCBI Gene 717016], HSPA8 (heat shock protein family A (Hsp70) member 8) [NCBI Gene 3312] {aka HEL-33, HEL-S-72p, HSC54, HSC70, HSC71, HSP71}, EIF1 (eukaryotic translation initiation factor 1) [NCBI Gene 10209] {aka A121, EIF-1, EIF1A, ISO1, SUI1}, TGFA (transforming growth factor alpha) [NCBI Gene 613031] {aka TGF alpha}, GPX4 (glutathione peroxidase 4) [NCBI Gene 705333], PRPH2 (peripherin 2) [NCBI Gene 696630] {aka RDS}
- **Diseases:** eye diseases (MESH:D005128), neurological diseases (MESH:D020271), HKGs (MESH:C537680), amenorrhea (MESH:D000568), polycystic ovary syndrome (MESH:D011085), myoclonic epilepsy (MESH:D004831), toxicity (MESH:D064420), Cancer (MESH:D009369), Bardet-Biedl Syndrome (MESH:D020788), hepatocellular carcinoma (MESH:D006528), Batten disease (MESH:D009472), lung cancer (MESH:D008175), rod-cone dystrophy (MESH:D000071700), glioblastoma (MESH:D005909), age-related or neurodegenerative diseases (MESH:D019636), and posterior staphyloma (MESH:C536352), cataract (MESH:D002386), Pelizaeus-Merzbacher disease (MESH:D020371), retinal dystrophy (MESH:D058499), oncological diseases (MESH:D000072716), of the reproductive system (MESH:D060737), hereditary nonpolyposis colorectal cancer syndrome (MESH:D003123), endometriosis (MESH:D004715), Coats-like retinopathy (MESH:D058456), oligomenorrhea (MESH:D009839), microcornea (MESH:C538287), Parkinson's disease (MESH:D010300), intellectual disability (MESH:D008607), von willebrand's disease (MESH:D014842), Huntington's disease (MESH:D006816), retinitis pigmentosa (MESH:D012174), Sedaghatian-type spondylometaphyseal dysplasia (MESH:C535798), left ventricular hypertrophy (MESH:D017379), neuroaxonal dystrophy (MESH:D019150), inherited retinal disease (MESH:D012164), colon cancer metastases (MESH:D015179), ophthalmologic diseases (MESH:D004194), mitochondrial encephalomyopathy (MESH:D017237), cervical cancer (MESH:D002583), syndrome (MESH:D013577), SCBMS (OMIM:616632), cardiovascular diseases (MESH:D002318), Parkinsons Dis (MESH:D003643), Alzheimer's disease (MESH:D000544), inherited ataxia (MESH:D013132)
- **Chemicals:** Orphanet (-), estradiol (MESH:D004958), MPTP (MESH:D015632), SYBR green (MESH:C098022), sulfatides (MESH:D013433)
- **Species:** Papio hamadryas (baboon, species) [taxon 9557], Macaca (macaque, genus) [taxon 9539], Macaca mulatta (rhesus macaque, species) [taxon 9544], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Cercopithecidae (monkey, family) [taxon 9527]
- **Cell lines:** H1299 — Homo sapiens (Human), Lung large cell carcinoma, Cancer cell line (CVCL_0060)

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12876923