Histone deacetylases are required for amphibian tail and limb regeneration but not development

Mechanisms of Development

Volumn 129, Issue 9-12, 2012, Pages 208-218

  Taylor, Amy J ^a   Beck, Caroline W ^a  

^a UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

Ambystoma mexicanum; Appendage; Epigenetic reprogramming; HDAC; Regeneration; Xenopus laevis

Indexed keywords

HISTONE DEACETYLASE;

ANIMAL EXPERIMENT; ARTICLE; CHROMATIN ASSEMBLY AND DISASSEMBLY; CONTROLLED STUDY; DEACETYLATION; EMBRYO; ENZYME ACTIVITY; ENZYME INHIBITION; HISTONE MODIFICATION; LIMB REGENERATION; NONHUMAN; PRIORITY JOURNAL; TAIL; TISSUE REGENERATION; TRANSCRIPTION REGULATION; XENOPUS LAEVIS;

AMBYSTOMA MEXICANUM; AMPHIBIANS; ANIMALS; BUTYRATES; EXTREMITIES; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HISTONE DEACETYLASE INHIBITORS; HISTONE DEACETYLASES; LARVA; REGENERATION; SODIUM CHANNEL BLOCKERS; SODIUM CHANNELS; TAIL; VALPROIC ACID; WOUND HEALING; XENOPUS LAEVIS;

AMBYSTOMA MEXICANUM; AMPHIBIA; XENOPUS LAEVIS;

EID: 84867896794     PISSN: 09254773     EISSN: 18726356     Source Type: Journal    
DOI: 10.1016/j.mod.2012.08.001     Document Type: Article

References (40)

1. Adams D.S., Masi A., Levin M. H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration. Development 2007, 134:1323-1335.
2. Beck C.W., Christen B., Slack J.M. Molecular pathways needed for regeneration of spinal cord and muscle in a vertebrate. Dev. Cell 2003, 5:429-439.
3. Beck C.W., Slack J.M. Notch is required for outgrowth of the Xenopus tail bud. Int. J. Dev. Biol. 2002, 46:255-258.
4. Beck C.W., Slack J.M.W. A developmental pathway controlling outgrowth of the Xenopus tail bud. Development 1999, 126:1611-1620.
5. Beck C.W., Belmonte J.C.I., Christen B. Beyond Early Development: Xenopus as an emerging model for the study of Regenerative mechanisms. Developmental Dynamics 2009, 238:1226-1248.
6. Bely A.E., Nyberg K.G. Evolution of animal regeneration: re-emergence of a field. Trends Ecol. Evol. 2010, 25:161-170.
7. Bordzilovskaya, N.P., Dettlaff, T.A., Duhon, S., Malacinski, G., 1989. Developmental-stage series of axolotl embryos. In: Armstrong, J.B., Malacinski, G. (Eds.), Developmental Biology of the Axolotl, Oxford University Press, New York, pp. 201-219.
8. Candido E.P., Reeves R., Davie J.R. Sodium butyrate inhibits histone deacetylation in cultured cells. Cell 1978, 14:105-113.
9. Christen B., Robles V., Raya M., Paramonov I., Belmonte J.C. Regeneration and reprogramming compared. BMC Biol. 2010, 8:5.
10. Davie J.R. Inhibition of histone deacetylase activity by butyrate. J. Nutr. 2003, 133:2485S-2493S.
11. Day R.C., Beck C.W. Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling. BMC Dev. Biol. 2011, 11:54.
12. Dent J.N. Limb regeneration in larvae and metamorphosing individuals of the South African clawed toad. J. Morphol. 1962, 110:61-77.
13. Detich N., Bovenzi V., Szyf M. Valproate induces replication-independent active DNA demethylation. J. Biol. Chem. 2003, 278:27586-27592.
14. Gargioli C., Slack J.M. Cell lineage tracing during Xenopus tail regeneration. Development 2004, 131:2669-2679.
15. Gottlicher M., Minucci S., Zhu P., Kramer O.H., Schimpf A., Giavara S., Sleeman J.P., Lo Coco F., Nervi C., Pelicci P.G., Heinzel T. Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells. EMBO J. 2001, 20:6969-6978.
16. Grow M., Neff A.W., Mescher A.L., King M.W. Global analysis of gene expression in Xenopus hindlimbs during stage-dependent complete and incomplete regeneration. Dev. Dyn. 2006, 235:2667-2685.
17. Gurvich N., Berman M.G., Wittner B.S., Gentleman R.C., Klein P.S., Green J.B.A. Association of valproate-induced teratogenesis with histone deacetylase inhibition in vivo. FASEB Journal 2005, 19:1166.
18. Jergil M., Kultima K., Gustafson A.L., Dencker L., Stigson M. Valproic acid-induced deregulation in vitro of genes associated in vivo with neural tube defects. Toxicol. Sci. 2009, 108:132-148.
19. King M.W., Mescher A.L., Harty M.W., Muzinich M.C., Smith R.C., Neff A.W. Expression of the Xenopus DECD-box RNA helicase, XDDX39, during development and limb regeneration. Dev. Biol. 2003, 259:534.
20. King M.W., Neff A.W., Mescher A.L. Proteomics analysis of regenerating amphibian limbs: changes during the onset of regeneration. Int. J. Dev. Biol. 2009, 53:955-969.
21. Kragl M., Knapp D., Nacu E., Khattak S., Maden M., Epperlein H.H., Tanaka E.M. Cells keep a memory of their tissue origin during axolotl limb regeneration. Nature 2009, 460:U60-U69.
22. Kramer O.H., Zhu P., Ostendorff H.P., Golebiewski M., Tiefenbach J., Peters M.A., Brill B., Groner B., Bach I., Heinzel T., Gottlicher M. The histone deacetylase inhibitor valproic acid selectively induces proteasomal degradation of HDAC2. EMBO J. 2003, 22:3411-3420.
23. Lenhoff H.M., Lenhoff S.G. Abraham Trembley and the origins of research on regeneration in animals. A History of Regeneration Research 1991, 47-65. Cambridge University Press, Cambridge. C.E. Dinsmore (Ed.).
24. Malloch E.L., Perry K.J., Fukui L., Johnson V.R., Wever J., Beck C.W., King M.W., Henry J.J. Gene expression profiles of lens regeneration and development in Xenopus laevis. Dev. Dyn. 2009, 238:2340-2356.
25. Mescher A.L. The cellular basis of limb regeneration in urodeles. Int. J. Dev. Biol. 1996, 40:785-795.
26. Nau, H., 1994. Valproic acid-induced neural tube defects. Ciba Found Symp. 181, 144-152 (discussion 152-160).
27. Nau H., Scott W.J. Teratogenicity of valproic acid and related substances in the mouse: drug accumulation and pHi in the embryo during organogenesis and structure-activity considerations. Arch. Toxicol. Suppl. 1987, 11:128-139.
28. Newman S.M., Dugan T.S., Dumont J.N. A rapid and simple procedure for visualization of amphibian skeletons for teratological studies. Trans. Am. Microscopical Soc. 1983, 102:300-305.
29. Nieuwkoop P., Faber J. Normal table of Xenopus laevis 1967, North Holland Publishing Co., Amsterdam.
30. Pearl E.J., Barker D., Day R.C., Beck C.W. Identification of genes associated with regenerative success of Xenopus laevis hindlimbs. BMC Dev. Biol. 2008, 8:66.
31. Perucca E. Pharmacological and therapeutic properties of valproate: a summary after 35 years of clinical experience. CNS Drugs 2002, 16:695-714.
32. Phiel C.J., Zhang F., Huang E.Y., Guenther M.G., Lazar M.A., Klein P.S. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J. Biol. Chem. 2001, 276:36734-36741.
33. Slack J.M., Beck C.W., Gargioli C., Christen B. Cellular and molecular mechanisms of regeneration in Xenopus. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2004, 359:745-751.
34. Slack J.M., Lin G., Chen Y. The Xenopus tadpole: a new model for regeneration research. Cell Mol. Life Sci. 2008, 65:54-63.
35. Tazaki A., Kitayama A., Terasaka C., Watanabe K., Ueno N., Mochii M. Macroarray-based analysis of tail regeneration in Xenopus laevis larvae. Dev. Dyn. 2005, 233:1394-1404.
36. Tseng A.S., Adams D.S., Qiu D., Koustubhan P., Levin M. Apoptosis is required during early stages of tail regeneration in Xenopus laevis. Dev. Biol. 2007, 301:62-69.
37. Tseng A.S., Beane W.S., Lemire J.M., Masi A., Levin M. Induction of vertebrate regeneration by a transient sodium current. J. Neurosci. 2010, 30:13192-13200.
38. Tseng, A.S., Carneiro, K., Lemire, J.M., Levin, M., 2011. HDAC Activity Is Required during Xenopus Tail Regeneration. PLoS One 6.
39. Tucker A.S., Slack J.M.W. The Xenopus-Laevis tail-forming region. Development 1995, 121:249-262.
40. Yakushiji N., Suzuki M., Satoh A., Sagai T., Shiroishi T., Kobayashi H., Sasaki H., Ide H., Tamura K. Correlation between Shh expression and DNA methylation status of the limb-specific Shh enhancer region during limb regeneration in amphibians. Dev. Biol. 2007, 312:171-182.