Evolution of animal regeneration: re-emergence of a field

Trends in Ecology and Evolution

Volumn 25, Issue 3, 2010, Pages 161-170

  Bely, Alexandra E ^a   Nyberg, Kevin G ^a  

^a Bldg 142   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; EVOLUTIONARY BIOLOGY; PHYLOGENETICS; REGENERATION;

ANIMAL; CHORDATA; EVOLUTION; INVERTEBRATE; PHYSIOLOGY; REGENERATION; REVIEW;

ANIMALS; CHORDATA; EVOLUTION; INVERTEBRATES; REGENERATION;

ANIMALIA;

EID: 76249112565     PISSN: 01695347     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tree.2009.08.005     Document Type: Review

References (99)

1. In: Dinsmore C.E. (Ed). A History of Regeneration Research: Milestones in the Evolution of a Science (1991), Cambridge University Press
2. Vorontsova M.A., and Liosner L.D. Asexual Propagation and Regeneration (1960), Pergamon Press
3. Goss R.J. Principles of Regeneration (1969), Academic Press
4. Alibardi L., and Toni M. Wound keratins in the regenerating epidermis of lizard suggests that the wound reaction is similar in the tail and limb. J. Exp. Zool. 303A (2005) 845-860
5. Bely A.E. Distribution of segment regeneration ability in the Annelida. Integr. Comp. Biol. 46 (2006) 508-518
6. Goss R.J. The evolution of regeneration: Adaptive or inherent? J. Theor. Biol. 159 (1992) 241-260
7. Reichman O.J. Evolution of regeneration capabilities. Am. Nat. 123 (1984) 752-763
8. Morgan T.H. Regeneration (1901), Macmillan
9. Weismann A. Regeneration: facts and interpretations. Nat. Sci. 14 (1899) 305-328
10. Wagner G.P., and Misof B.Y. Evolutionary modification of regenerative capability in vertebrates: a comparative study on teleost pectoral fin regeneration. J. Exp. Zool. 261 (1992) 62-78
11. Lengfeld T., et al. Multiple Wnts are involved in Hydra organizer formation and regeneration. Dev. Biol. 330 (2009) 186-199
12. Brockes J.P., and Kumar A. Comparative aspects of animal regeneration. Annu. Rev. Cell. Dev. Biol. 24 (2008) 525-549
13. Bely A.E., and Wray G.A. Evolution of regeneration and fission in annelids: insights from engrailed- and orthodenticle-class gene expression. Development 128 (2001) 2781-2791
14. Bely A.E. Decoupling of fission and regenerative capabilities in an asexual oligochaete. Hydrobiologia 406 (1999) 243-251
15. Fleming P.A., et al. Leave it all behind: a taxonomic perspective of autotomy in invertebrates. Biol. Rev. 82 (2007) 481-510
16. Rinkevich Y., et al. Systemic bud induction and retinoic acid signaling underlie whole body regeneration in the urochordate Botrylloides leachi. PLoS Biol. 5 (2007) e71
17. Bernardo J., and Agosta S.J. Evolutionary implications of hierarchical impacts of nonlethal injury on reproduction, including maternal effects. Biol. J. Linn. Soc. 86 (2005) 309-331
18. Carlson B.M. Principles of Regenerative Biology (2007), Academic Press
19. Illingworth C.M. Trapped fingers and amputated finger tips in children. J. Pediatr. Surg. 9 (1974) 853-858
20. Han M., et al. Development and regeneration of the neonatal digit tip in mice. Dev. Biol. 315 (2008) 125-135
21. Williams-Boyce P.K., and Daniel Jr. J.C. Comparison of ear tissue regeneration in mammals. J. Anat. 149 (1986) 55-63
22. Kierdorf U., et al. Deer antler regeneration: cells, concepts, and controversies. J. Morphol. 268 (2007) 726-738
23. Agata K., et al. Unifying principles of regeneration I: Epimorphosis versus morphallaxis. Dev. Growth Differ. 49 (2007) 73-78
24. Sánchez Alvarado A., and Tsonis P.A. Bridging the regeneration gap: genetic insights from diverse animal models. Nat. Rev. Genet. 7 (2006) 873-884
25. Galliot B., and Schmid V. Cnidarians as a model system for understanding evolution and regeneration. Int. J. Dev. Biol. 46 (2002) 39-48
26. Martin P., and Parkhurst S.M. Parallels between tissue repair and embryo morphogenesis. Development 131 (2004) 3021-3034
27. Kato K., et al. Dorsal and ventral positional cues required for the onset of planarian regeneration may reside in differentiated cells. Dev. Biol. 233 (2001) 109-121
28. Campbell L.J., and Crews C.M. Wound epidermis formation and function in urodele amphibian limb regeneration. Cell. Mol. Life Sci. 65 (2008) 73-79
29. Bosch T.C.G. Why polyps regenerate and we don't: Towards a cellular and molecular framework for Hydra regeneration. Dev. Biol. 303 (2007) 421-433
30. Quiñones J.L., et al. Extracellular matrix remodeling and metalloproteinase involvement during intestine regeneration in the sea cucumber Holothuria glaberrima. Dev. Biol. 250 (2002) 181-197
31. Yokoyama H. Initiation of limb regeneration: the critical steps for regenerative capacity. Dev. Growth Differ. 50 (2008) 13-22
32. Levin M. Large-scale biophysics: ion flows and regeneration. Trends Cell Biol. 17 (2007) 261-270
33. Adams D.S., et al. H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration. Development 134 (2007) 1323-1335
34. Kimura Y., et al. Expression of complement 3 and complement 5 in newt limb and lens regeneration. J. Immunol. 170 (2003) 2331-2339
35. Ramírez-Gómez F., et al. Immune-related genes associated with intestinal tissue in the sea cucumber Holothuria glaberrima. Immunogenetics 60 (2008) 57-71
36. Lin G., and Slack J.M. Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration. Dev. Biol. 316 (2008) 323-335
37. Gurley K.A., et al. β-catenin defines head versus tail identity during planarian regeneration and homeostasis. Science 319 (2008) 323-327
38. Nakamura T., et al. EGFR signaling is required for re-establishing the proximodistal axis during distal leg regeneration in the cricket Gryllus bimaculatus nymph. Dev. Biol. 319 (2008) 46-55
39. Adell T., et al. Smed-Evi/Wntless is required for β-catenin-dependent and -independent processes during planarian regeneration. Development 136 (2009) 905-910
40. Kumar A., et al. Molecular basis for the nerve dependence of limb regeneration in an adult vertebrate. Science 318 (2007) 772-777
41. Monaghan J.R., et al. Microarray and cDNA sequence analysis of transcription during nerve-dependent limb regeneration. BMC Biol. 7 (2009) 1
42. Berrill N.J. Regeneration and budding in worms. Biol. Rev. 27 (1952) 401-438
43. Biressi A.C.M., et al. Wound healing and arm regeneration in Ophioderma longicaudum and Amphiura filiformis (Ophiuroidea, Echinodermata): comparative morphogenesis and histogenesis. Zoomorphology 129 (2010) 1-19
44. Kragl M., et al. Cells keep a memory of their tissue origin during axolotl limb regeneration. Nature 460 (2009) 60-65
45. Candia Carnevali M.D. Regeneration in echinoderms: repair, regrowth, cloning. Invert. Surv. J. 3 (2006) 64-76
46. Halanych K.M. The new view of animal phylogeny. Annu. Rev. Ecol. Syst. 35 (2004) 229-256
47. Kawamura K., et al. Multipotent epithelial cells in the process of regeneration and asexual reproduction in colonial tunicates. Dev. Growth Differ. 50 (2008) 1-11
48. Martinez V.G., et al. Regeneration and asexual reproduction share common molecular changes: upregulation of a neural glycoepitope during morphallaxis in Lumbriculus. Mech. Dev. 122 (2005) 721-732
49. Burton P.M., and Finnerty J.R. Conserved and novel gene expression between regeneration and asexual fission in Nematostella vectensis. Dev. Genes Evol. 219 (2009) 79-87
50. Ghosh S., et al. Analysis of the expression and function of Wnt-5a and Wnt-5b in developing and regenerating axolotl (Ambystoma mexicanum) limbs. Dev. Growth Differ. 50 (2008) 289-297
51. Huntley J.W., and Kowaleski M. Strong coupling of predation intensity and diversity in the Phanerozoic fossil record. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 15006-15010
52. Wulff J.L. Resistance vs recovery: morphological strategies of coral reef sponges. Funct. Ecol. 20 (2006) 699-708
53. Lawrence J.M., and Vásquez J. The effect of sublethal predation on the biology of echinoderms. Oceanol. Acta 19 (1996) 431-440
54. Baumiller T.K., and Gahn F.J. Testing predator-driven evolution with Paleozoic crinoid arm regeneration. Science 305 (2004) 1453-1455
55. Juanes F., and Smith L.D. The ecological consequences of limb damage and loss in decapod crustaceans: a review and prospectus. J. Exp. Mar. Biol. Ecol. 193 (1995) 197-223
56. Robinson J.V. The ecological role of caudal lamellae loss in the larval damselfly, Ischnura posita (Hagen) (Odonata: Zygoptera). Oecologia 87 (1991) 1-7
57. Meyer J.J., and Byers J.E. As good as dead? Sublethal predation facilitates lethal predation on an intertidal clam. Ecol. Lett. 8 (2005) 160-166
58. De Vlas J. Annual food intake by plaice and flounder in a tidal flat area in the Dutch Wadden Sea, with special reference to consumption of regenerating parts of macrobenthic prey. Neth. J. Sea Res. 13 (1979) 117-153
59. Henry L.-A., and Hart M. Regeneration from injury and resource allocation in sponges and corals - a review. Int. Rev. Hydrobiol. 90 (2005) 125-158
60. Clark M.S., et al. Delayed arm regeneration in the Antarctic brittle star Ophionotus victoriae. Aquat. Biol. 1 (2007) 45-53
61. Shargal E., et al. Ecological and histological aspects of tail loss in spiny mice (Rodentia: Muridae, Acomys) with a review of its occurrence in rodents. J. Zool. 249 (1999) 187-193
62. Maginnis T.L. The costs of autotomy and regeneration in animals: a review and framework for future research. Behav. Ecol. 17 (2006) 857-872
63. Bateman P.W., and Fleming P.A. To cut a long tail short: a review of lizard caudal autotomy studies carried out over the last 20 years. J. Zool. 277 (2009) 1-14
64. Gillis G.B., et al. Losing stability: tail loss and jumping in the arboreal lizard Anolis carolinensis. J. Exp. Biol. 212 (2009) 604-609
65. Naya D.E., et al. Some vaguely explored (but not trivial) costs of tail autotomy in lizards. Comp. Biochem. Physiol., A: Mol. Integr. Physiol. 146 (2007) 189-193
66. Wrinn K.M., and Uetz G.W. Effects of autotomy and regeneration on detection and capture of prey in a generalist predator. Behav. Ecol. 19 (2008) 1282-1288
67. Lutzy R.M., and Morse D.H. Effects of leg loss on male crab spiders Misumena vatia. Anim. Behav. 76 (2008) 1519-1527
68. Guffey C. Costs associated with leg autotomy in the harvestmen Leiobunum nigripes and Leiobunum vittatum (Arachnida: Opiliones). Can. J. Zool. 77 (1999) 824-830
69. Brueseke M.A., et al. Leg autotomy in the wolf spider Pardosa milvina: a common phenomenon with few apparent costs. Am. Midl. Nat. 146 (2001) 153-160
70. Brautigam S.E., and Persons M.H. The effect of limb loss on the courtship and mating behavior of the wolf spider Pardosa milvina (Araneae: Lycosidae). J. Insect Behav. 16 (2003) 571-587
71. Galis F., et al. Why is limb regeneration possible in amphibians but not in reptiles, birds, and mammals?. Evol. Dev. 5 (2003) 208-220
72. Fox S.F., and McCoy J.K. The effects of tail loss on survival, growth, reproduction, and sex ratio of offspring in the lizard Uta stansburiana in the field. Oecologia 122 (2000) 327-334
73. Vollrath F. Leg regeneration in web spiders and its implications for orb weaver phylogeny. Bull. Br. Arachnol. Soc. 8 (1990) 177-184
74. Scadding S.R. Limb regeneration in adult amphibia. Can. J. Zool. 59 (1981) 34-46
75. Arnold E.N. Evolutionary aspects of tail shedding in lizards and their relatives. J. Nat. Hist. 18 (1984) 127-169
76. Beck C.W., et al. Molecular pathways needed for regeneration of spinal cord and muscle in a vertebrate. Dev. Cell 5 (2003) 429-439
77. Fukazawa T., et al. Suppression of the immune response potentiates tadpole tail regeneration during the refractory period. Development 136 (2009) 2323-2327
78. Tomiyama T., et al. Feeding and growth of juvenile stone flounder in esturaries: generality and the importance of sublethal tissue cropping of benthic invertebrates. Mar. Biol. 151 (2007) 365-376
79. Gahn F.J., and Baumiller T.K. Arm regeneration in Mississippian crinoids: evidence of intense predation pressure in the Paleozoic?. Paleobiology 31 (2005) 151-164
80. Sasaki K., et al. Predation pressure on the siphons of the bivalve Nuttallia olivacea by the juvenile stone flounder Platichthys bicoloratus in the Natori River estuary, north-eastern Japan. Fish. Sci. 68 (2002) 104-116
81. Maginnis T.L. Autotomy in a stick insect (Insecta: Phasmida): predation versus molting. Fla. Entomol. 91 (2008) 126-127
82. Moore A., et al. Leg autotomy: a novel mechanism of protection against insecticide poisoning in diamondback moth (Lepidoptera: Plutellidae). J. Econ. Entomol. 82 (1989) 1295-1298
83. Vidal D.E., and Horne A.J. Mercury toxicity in the aquatic oligochaete Sparganophilus pearsei II: autotomy as a novel form of protection. Arch. Environ. Contam. Toxicol. 45 (2003) 462-467
84. Wilkie I.C. Autotomy as a prelude to regeneration in echinoderms. Microsc. Res. Tech. 55 (2001) 369-396
85. McGaw I.J. Cardiovascular and respiratory responses associated with limb autotomy in the blue crab, Callinectes sapidus. Mar. Freshwat. Behav. Physiol. 39 (2006) 131-141
86. Martínez D.E. Rejuvenation of the disposable soma: repeated injury extends lifespan in an asexual annelid. Exp. Gerontol. 31 (1996) 699-704
87. Lindsay S.M., and Woodin S.A. Tissue loss induces switching of feeding mode in spionid polychaetes. Mar. Ecol. Prog. Ser. 125 (1995) 159-169
88. Cooper W.E. How to stay alive after losing your tail. Behav. 145 (2008) 1085-1099
89. Taylor P.W., et al. Compensation for injury? Modified multi-modal courtship of wolf spiders following autotomy of signalling appendages. Ethol. Ecol. Evol. 18 (2006) 79-89
90. Barrios J.V., et al. Effect of the degree of autotomy on feeding, growth, and reproductive capacity in the multi-armed sea star Heliaster helianthus. J. Exp. Mar. Biol. Ecol. 361 (2008) 21-27
91. Ramos M., et al. Overcoming an evolutionary conflict: Removal of a reproductive organ greatly increases locomotor performance. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 4883-4887
92. Lindsay S.M., et al. Morphology of anterior regeneration in two spionid polychaete species: implications for feeding efficiency. Invertebr. Biol. 127 (2008) 65-79
93. Dupont S., and Thorndyke M.C. Growth or differentiation? Adaptive regeneration in the brittlestar Amphiura filiformis. J. Exp. Biol. 209 (2006) 3873-3881
94. Maginnis T.L. Leg regeneration stunts wing growth and hinders flight performance in a stick insect (Sipyloidea sipylus). Proc. R. Soc. Lond. B 273 (2006) 1811-1814
95. Lailvaux S.P., et al. Dishonest signalling of fighting ability and multiple performance traits in the fiddler crab Uca mjoebergi. Funct. Ecol. 23 (2009) 359-366
96. Vitt L.J., and Cooper W.E. Tail loss, tail color and predator escape in Eumeces (Lacertilia: Scincidae): age-specific differences in costs and benefits. Can. J. Zool. 64 (1986) 583-592
97. Giribet G. Assembling the lophotrochozoan (=spiralian) tree of life. Philos. Trans. R. Soc. B 363 (2008) 1513-1522
98. Telford M.J., et al. The evolution of the Ecdysozoa. Philos. Trans. R. Soc. B 363 (2008) 1529-1537
99. Swalla B.J., and Smith A.B. Deciphering deuterostome phylogeny: molecular, morphological and palaeontological perspectives. Phil Trans R Soc B 363 (2008) 1557-1568