Identification of differentially expressed genes in scarless wound healing utilizing polymerase chain reaction-suppression subtractive hybridization

Wound Repair Regen. 2006 Jul-Aug;14(4):413-20. doi: 10.1111/j.1743-6109.2006.00140.x.

Abstract

Wound healing in fetal skin is well known to proceed without scarring, whereas adult (postnatal) skin wound healing is accompanied by scar formation. To identify differentially expressed genes during fetal wound (FW) healing, we have used polymerase chain reaction-suppression subtractive hybridization. This technique allows for a comparative analysis across the entire transcriptome of FW vs. unwounded fetal control tissue, including even potentially novel sequences. Our subtractive hybridization protocol identified 15 clones that are overexpressed in healing FWs, and 20 clones that are underexpressed. These include genes with both known and unknown functions. We have confirmed the differential pattern of expression for four of these candidate genes: elongation factor 1 alpha, elongation initiation factor 4e, and two transcripts thus far known only as an expressed sequence tags. With this approach, we have also identified novel genes potentially involved in scarless wound healing.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cicatrix / genetics*
  • Eukaryotic Initiation Factor-4E / genetics
  • Eukaryotic Initiation Factor-4E / metabolism
  • Expressed Sequence Tags / metabolism
  • Fetus
  • Peptide Elongation Factor 1 / genetics
  • Peptide Elongation Factor 1 / metabolism
  • Polymerase Chain Reaction
  • Rabbits
  • Skin / injuries*
  • Wound Healing / genetics*
  • Wounds, Penetrating / genetics
  • Wounds, Penetrating / metabolism
  • Wounds, Penetrating / physiopathology*

Substances

  • Eukaryotic Initiation Factor-4E
  • Peptide Elongation Factor 1