# Restoring Ag1, an ancient regeneration gene lost in amniotes, accelerates skin healing in mice

**Authors:** Anastasiya V. Kosykh, Elena B. Zhigmitova, Nadezhda A. Evtushenko, Tatyana H. Gurskaia, Aleksandra A. Martynova, Yuliya Yu. Silaeva, Anastasiia S. Ivanova, Natalia Y. Martynova, Maria B. Tereshina, Stanislav G. Rudyak, Andrey A. Panteleyev, Helen P. Makarenkova, Nadya G. Gurskaya, Sergey A. Lukyanov, Andrey G. Zaraisky

PMC · DOI: 10.3389/fcell.2026.1706902 · Frontiers in Cell and Developmental Biology · 2026-02-19

## TL;DR

Scientists restored an ancient gene in mice and found it speeds up skin healing, suggesting lost genes could help modern animals repair tissues better.

## Contribution

The study shows that reintroducing a regeneration gene lost in amniotes can enhance wound healing in mice.

## Key findings

- Inducing Ag1 in mice skin led to 20% faster wound closure.
- Transcriptomic analysis showed activation of wound repair pathways and genes linked to scarless healing.
- Ancient Ag1 gene can stimulate tissue repair in modern mammals despite being lost over 300 million years ago.

## Abstract

Tissue and organ regeneration is a remarkable ability observed in many animal species, which has been significantly reduced or lost in several vertebrate lineages, partly due to the evolutionary loss of regeneration-associated genes. For example, many genes involved in limb and skin regeneration in anamniotes (fish and amphibians) have been lost in amniotes (reptiles, birds, and mammals) following their transition to terrestrial life. This raises the intriguing question of whether reintroducing such lost genes could partially restore regenerative abilities. Here, we investigated whether the ag1 gene, which plays a key role in regeneration in fish and amphibians and was lost in amniotes, could enhance skin wound healing in mice. We generated transgenic mice with inducible expression of the Xenopus laevis ag1 gene in the skin and compared wound healing dynamics between induced and non-induced groups. Induction of ag1 resulted in approximately 20% faster wound closure. Transcriptomic analysis revealed enhanced activation of multiple pathways involved in wound repair and, notably, the upregulation of a subset of genes typically associated with scarless healing in amphibians and mammalian fetuses. Altogether, our findings demonstrate that a gene lost more than 300 million years ago can still stimulate reparative processes in mammalian tissues, highlighting the potential of ancient gene reactivation to enhance tissue repair in modern vertebrates.

## Linked entities

- **Genes:** TXNDC12 (thioredoxin domain containing 12) [NCBI Gene 51060]
- **Species:** Xenopus laevis (taxon 8355), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cxcl12 (C-X-C motif chemokine ligand 12) [NCBI Gene 20315] {aka Pbsf, Scyb12, Sdf1, Tlsf, Tpar1}, Ccl8 (C-C motif chemokine ligand 8) [NCBI Gene 20307] {aka 1810063B20Rik, HC14, MCP-2, Mcp2, Scya8}, Col6a1 (collagen, type VI, alpha 1) [NCBI Gene 12833] {aka Col6a-1}, Tgfb3 (transforming growth factor, beta 3) [NCBI Gene 21809] {aka TGF-beta-3, Tgfb-3}, Dmp1 (dentin matrix protein 1) [NCBI Gene 13406] {aka AG1, DMP-1, Dmp, PP}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Ctnnb1 (catenin beta 1) [NCBI Gene 12387] {aka Bfc, Catnb, Mesc}, SLC25A21 (solute carrier family 25 member 21) [NCBI Gene 89874] {aka MTDPS18, ODC, ODC1}, Mmp14 (matrix metallopeptidase 14 (membrane-inserted)) [NCBI Gene 17387] {aka MMP-X1, MT-MMP-1, MT1-MMP, sabe}, Brp1 (brain protein 1) [NCBI Gene 109667] {aka A1, Brp-1}, Epcam (epithelial cell adhesion molecule) [NCBI Gene 17075] {aka CD326, EGP, EGP-2, Egp314, Ep-CAM, EpCAM1}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, Thbs3 (thrombospondin 3) [NCBI Gene 21827] {aka TSP3, Thbs-3}, Tinagl1 (tubulointerstitial nephritis antigen-like 1) [NCBI Gene 94242] {aka 1110021J17Rik, AZ-1, AZ1, Arg1, Lcn7, TARP}, Col1a1 (collagen, type I, alpha 1) [NCBI Gene 12842] {aka Col1a-1, Cola-1, Cola1, Mov-13, Mov13}, Twist1 (twist basic helix-loop-helix transcription factor 1) [NCBI Gene 22160] {aka M-Twist, Pde, Ska10, Ska<m10Jus>, Twist, bHLHa38}, Agr3 (anterior gradient 3) [NCBI Gene 403205] {aka BCMP11, E030025L21Rik, Gm888}, Ccl7 (C-C motif chemokine ligand 7) [NCBI Gene 20306] {aka MCP-3, Scya7, fic, marc, mcp3}, Prrx2 (paired related homeobox 2) [NCBI Gene 20204] {aka Prx2, S8}, Agr2 (anterior gradient 2) [NCBI Gene 23795] {aka Agr2h, Gob-4, HAG-2, XAG-2, mAG-2}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, AGR2 (anterior gradient 2, protein disulphide isomerase family member) [NCBI Gene 10551] {aka AG-2, AG2, GOB-4, HAG-2, HEL-S-116, HPC8}, Prrx1 (paired related homeobox 1) [NCBI Gene 18933] {aka A230024N07Rik, K-2, MHox1, Pmx, Pmx1, Prx1}, Acta2 (actin alpha 2, smooth muscle, aorta) [NCBI Gene 11475] {aka 0610041G09Rik, Actvs, SMAalpha, SMalphaA, a-SMA, alphaSMA}, Tnc (tenascin C) [NCBI Gene 21923] {aka C130033P17Rik, Hxb, TN, TN-C, Ten, cytotactin}, Cd59a (CD59a antigen) [NCBI Gene 12509] {aka Cd59, MAC-IP, MACIF}, Col6a3 (collagen, type VI, alpha 3) [NCBI Gene 12835] {aka Col6a-3}, EEF1A2 (eukaryotic translation elongation factor 1 alpha 2) [NCBI Gene 1917] {aka DEE33, EEF1AL, EF-1-alpha-2, EF1A, EIEE33, HS1}, Col5a2 (collagen, type V, alpha 2) [NCBI Gene 12832] {aka 1110014L14Rik}, St3gal5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5) [NCBI Gene 20454] {aka 3S-T, Siat9, [a]2}, Egfr (epidermal growth factor receptor) [NCBI Gene 13649] {aka 9030024J15Rik, Erbb, Errb1, Errp, Wa5, wa-2}, Ccl21a (C-C motif chemokine ligand 21 (serine)) [NCBI Gene 18829] {aka 6CKBAC2, 6Ckine, ALP, CKb9, Gm1987, SCYA21a}, Col1a2 (collagen, type I, alpha 2) [NCBI Gene 12843] {aka Col1a-2, Cola-2, Cola2, oim}, TXNDC12 (thioredoxin domain containing 12) [NCBI Gene 51060] {aka AG1, AGR1, ERP16, ERP18, ERP19, PDIA16}, Mmp2 (matrix metallopeptidase 2) [NCBI Gene 17390] {aka Clg4a, GelA, MMP-2}, Col3a1 (collagen, type III, alpha 1) [NCBI Gene 12825] {aka Col3a-1, Tsk-2, Tsk2}, Col6a2 (collagen, type VI, alpha 2) [NCBI Gene 12834] {aka Col6a-2}, Tgfbr2 (transforming growth factor, beta receptor II) [NCBI Gene 21813] {aka 1110020H15Rik, DNIIR, RIIDN, TBR-II, TbetaR-II, TbetaRII}, Col6a4 (collagen, type VI, alpha 4) [NCBI Gene 68553] {aka 1110001D15Rik, Dvwa, EG235580, Vwa6}, Twist2 (twist basic helix-loop-helix transcription factor 2) [NCBI Gene 13345] {aka Dermo1, bHLHa39}
- **Diseases:** Neurogenic inflammation (MESH:D020078), cancers (MESH:D009369), inflammation (MESH:D007249), fibrosis (MESH:D005355), analgesia (MESH:D000699), keloid scars (MESH:D002921)
- **Chemicals:** NBF (-), hydrogen peroxide (MESH:D006861), tetracycline (MESH:D013752), hematoxylin (MESH:D006416), 3,3'-diaminobenzidine (MESH:D015100), eosin (MESH:D004801), PBS (MESH:D007854), HS (MESH:D006859), DAB (MESH:C000469), DAPI (MESH:C007293), calcium (MESH:D002118), ampicillin (MESH:D000667), citrate (MESH:D019343), CO2 (MESH:D002245), glutamine (MESH:D005973), chloroform (MESH:D002725), paraformaldehyde (MESH:C003043), Sepharose (MESH:D012685), tamoxifen (MESH:D013629), His (MESH:D006639), nitrogen (MESH:D009584), 2,2,2-tribromoethanol (MESH:C062527), carprofen (MESH:C007005), boric acid (MESH:C032688), doxycycline (MESH:D004318), paraffin (MESH:D010232), NaCl (MESH:D012965), silicone (MESH:D012828), cyanogen-bromide (MESH:D003488), STOP (MESH:D014002), isopropanol (MESH:D019840), HCl (MESH:D006851), ethanol (MESH:D000431), glycine (MESH:D005998), hyaluronic acid (MESH:D006820), FuGENE-6 (MESH:C411955)
- **Species:** Homo sapiens (human, species) [taxon 9606], Ambystoma mexicanum (axolotl, species) [taxon 8296], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Xenopus laevis (African clawed frog, species) [taxon 8355], Moloney murine leukemia virus (no rank) [taxon 11801], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** C-95  C, T2A, C +- 1  C
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038), pKB2 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_A628), fibroblasts — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594), Lenti-ag1 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_A4EW), 293T — Homo sapiens (Human), Transformed cell line (CVCL_0063)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960510/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960510/full.md

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Source: https://tomesphere.com/paper/PMC12960510