Title | Comparative expression profiling reveals an essential role for raldh2 in epimorphic regeneration. |
Publication Type | Journal Article |
Year of Publication | 2009 |
Authors | Mathew, LK, Sengupta, S, Franzosa, JA, Perry, J, La Du, J, Andreasen, EA, Tanguay, RL |
Journal | J Biol Chem |
Volume | 284 |
Issue | 48 |
Pagination | 33642-53 |
Date Published | 2009 Nov 27 |
ISSN | 1083-351X |
Keywords | Animals, Butadienes, Cluster Analysis, Embryo, Nonmammalian, Extremities, Female, Gene Expression Profiling, Gene Expression Regulation, Developmental, In Situ Hybridization, Larva, Male, Mitogen-Activated Protein Kinase 1, Mitogen-Activated Protein Kinase 3, Nitriles, Oligonucleotide Array Sequence Analysis, Pyrroles, Receptor, Fibroblast Growth Factor, Type 1, Regeneration, Retinal Dehydrogenase, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction, Wnt Proteins, Wound Healing, Zebrafish, Zebrafish Proteins |
Abstract | Zebrafish have the remarkable ability to regenerate body parts including the heart and fins by a process referred to as epimorphic regeneration. Recent studies have illustrated that similar to adult zebrafish, early life stage larvae also possess the ability to regenerate the caudal fin. A comparative microarray analysis was used to determine the degree of conservation in gene expression among the regenerating adult caudal fin, adult heart, and larval fin. Results indicate that these tissues respond to amputation/injury with strikingly similar genomic responses. Comparative analysis revealed raldh2, a rate-limiting enzyme for the synthesis of retinoic acid, as one of the most highly induced genes across the three regeneration platforms. In situ localization and functional studies indicate that raldh2 expression is critical for the formation of wound epithelium and blastema. Patterning during regenerative outgrowth was considered to be the primary function of retinoic acid signaling; however, our results suggest that it is also required for early stages of tissue regeneration. Expression of raldh2 is regulated by Wnt and fibroblast growth factor/ERK signaling. |
DOI | 10.1074/jbc.M109.011668 |
Alternate Journal | J. Biol. Chem. |
PubMed ID | 19801676 |
PubMed Central ID | PMC2785206 |
Grant List | P40 RR012546 / RR / NCRR NIH HHS / United States ES00210 / ES / NIEHS NIH HHS / United States P30 ES003850 / ES / NIEHS NIH HHS / United States P40 RR12546 / RR / NCRR NIH HHS / United States ES03850 / ES / NIEHS NIH HHS / United States ES10820 / ES / NIEHS NIH HHS / United States R01 ES010820 / ES / NIEHS NIH HHS / United States P30 ES000210 / ES / NIEHS NIH HHS / United States |