Allele-specific expression reveals genetic drivers of tissue regeneration in mice
Summary In adult mammals, skin wounds typically heal by scarring rather than through regeneration. In contrast, “super-healer” MRL mice have the unusual ability to regenerate ear punch wounds, yet the molecular basis for this regeneration remains elusive. Here, in hybrid crosses between MRL and non-regenerating mice, we use allele-specific gene expression to identifycis-regulatory variation associated with ear regeneration. Analyzing three major wound cell populations, we identified extensive strain- and tissue- specificcis-regulatory divergence associated with differences in healing outcomes. Genes withcis-regulatory differences specifically in fibroblasts were associated with wound healing phenotypes and pathways, and were enriched near genetic markers associated with ear-healing in a genetic cross. Finally, we demonstrated that one of these genes,Cfh, could be applied ectopically to accelerate wound repair and induce regeneration in typically fibrotic wounds. Overall, our results provide insight into the molecular drivers of regeneration in MRL mice with potential clinical implications..
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Preprint| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
bioRxiv.org - (2023) vom: 20. Feb. Zur Gesamtaufnahme - year:2023 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Talbott, Heather E. [VerfasserIn] |
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| Links: |
Volltext [kostenfrei] |
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| Themen: |
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| doi: |
10.1101/2022.09.23.509223 |
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| PPN (Katalog-ID): |
XBI037404814 |
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| 100 | 1 | |a Talbott, Heather E. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Allele-specific expression reveals genetic drivers of tissue regeneration in mice |
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| 520 | |a Summary In adult mammals, skin wounds typically heal by scarring rather than through regeneration. In contrast, “super-healer” MRL mice have the unusual ability to regenerate ear punch wounds, yet the molecular basis for this regeneration remains elusive. Here, in hybrid crosses between MRL and non-regenerating mice, we use allele-specific gene expression to identifycis-regulatory variation associated with ear regeneration. Analyzing three major wound cell populations, we identified extensive strain- and tissue- specificcis-regulatory divergence associated with differences in healing outcomes. Genes withcis-regulatory differences specifically in fibroblasts were associated with wound healing phenotypes and pathways, and were enriched near genetic markers associated with ear-healing in a genetic cross. Finally, we demonstrated that one of these genes,Cfh, could be applied ectopically to accelerate wound repair and induce regeneration in typically fibrotic wounds. Overall, our results provide insight into the molecular drivers of regeneration in MRL mice with potential clinical implications. | ||
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| 700 | 1 | |a Mack, Katya L. |0 (orcid)0000-0003-0484-4553 |4 aut | |
| 700 | 1 | |a Griffin, Michelle |4 aut | |
| 700 | 1 | |a Guardino, Nicholas J. |4 aut | |
| 700 | 1 | |a Parker, Jennifer B.L. |4 aut | |
| 700 | 1 | |a Spielman, Amanda F. |4 aut | |
| 700 | 1 | |a Davitt, Michael F. |4 aut | |
| 700 | 1 | |a Mascharak, Shamik |4 aut | |
| 700 | 1 | |a Berger, Mark J. |4 aut | |
| 700 | 1 | |a Wan, Derrick C. |4 aut | |
| 700 | 1 | |a Fraser, Hunter B. |4 aut | |
| 700 | 1 | |a Longaker, Michael T. |4 aut | |
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