The Genetic Architecture of Skeletal Convergence and Sex Determination in Ninespine Sticklebacks (DOI:10.1016/j.cub.2009.05.029);The Genetic Architecture of Skeletal Convergence and Sex Determination in Ninespine Sticklebacks

Current Biology

Volumn 19, Issue 13, 2009, Pages 1140-1145

  Shapiro, Michael D ^a   Summers, Brian R ^b   Balabhadra, Sarita ^b   Aldenhoven, Jaclyn T ^a   Miller, Ashley L ^a   Cunningham, Christopher B ^a   Bell, Michael A ^c   Kingsley, David M ^b  

^a UNIVERSITY OF UTAH   (United States)

^b STANFORD UNIVERSITY   (United States)

^c STONY BROOK UNIVERSITY   (United States)

Author keywords

DNA; EVOL_ECOL

Indexed keywords

ANIMALIA; GASTEROSTEUS; GASTEROSTEUS ACULEATUS; PUNGITIUS; PUNGITIUS PUNGITIUS; VERTEBRATA;

EID: 67649834521     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2009.06.027     Document Type: Erratum

References (59)

1. Arendt J., and Reznick D. Convergence and parallelism reconsidered: What have we learned about the genetics of adaptation?. Trends Ecol. Evol. 23 (2008) 26-32
2. Gould S.J. The Structure of Evolutionary Theory (2002), The Belknap Press of Harvard University Press, Cambridge, MA
3. Peichel C.L., Nereng K., Ohgi K.A., Cole B.L.E., Colosimo P.F., Buerkle C.A., Schluter D., and Kingsley D.M. The genetic architecture of divergence between threespine stickleback species. Nature 414 (2001) 901-905
4. Shapiro M.D., Marks M.E., Peichel C.L., Blackman B.K., Nereng K.S., Jonsson B., Schluter D., and Kingsley D.M. Genetic and developmental basis of evolutionary pelvic reduction in threespine sticklebacks. Nature 428 (2004) 717-723
5. Colosimo P.F., Peichel C.L., Nereng K., Blackman B.K., Shapiro M.D., Schluter D., and Kingsley D.M. The genetic architecture of parallel armor plate reduction in threespine sticklebacks. PLoS Biol. 2 (2004) e109
6. Cresko W.A., Amores A., Wilson C., Murphy J., Currey M., Phillips P., Bell M.A., Kimmel C.B., and Postlethwait J.H. Parallel genetic basis for repeated evolution of armor loss in Alaskan threespine stickleback populations. Proc. Natl. Acad. Sci. USA 101 (2004) 6050-6055
7. Peichel C.L., Ross J.A., Matson C.K., Dickson M., Grimwood J., Schmutz J., Myers R.M., Mori S., Schluter D., and Kingsley D.M. The master sex-determination locus in threespine sticklebacks is on a nascent y chromosome. Curr. Biol. 14 (2004) 1416-1424
8. Colosimo P.F., Hosemann K.E., Balabhadra S., Villarreal Jr. G., Dickson M., Grimwood J., Schmutz J., Myers R.M., Schluter D., and Kingsley D.M. Widespread parallel evolution in sticklebacks by repeated fixation of Ectodysplasin alleles. Science 307 (2005) 1928-1933
9. Kimmel C.B., Ullmann B., Walker C., Wilson C., Currey M., Phillips P.C., Bell M.A., Postlethwait J.H., and Cresko W.A. Evolution and development of facial bone morphology in threespine sticklebacks. Proc. Natl. Acad. Sci. USA 102 (2005) 5791-5796
10. Miller C.T., Beleza S., Pollen A.A., Schluter D., Kittles R.A., Shriver M.D., and Kingsley D.M. cis-regulatory changes in Kit ligand expression and parallel evolution of pigmentation in sticklebacks and humans. Cell 131 (2007) 1179-1189
11. Cole N.J., Tanaka M., Prescott A., and Tickle C.A. Expression of limb initiation genes and clues to the basis of morphological diversification in threespine sticklebacks. Curr. Biol. 13 (2003) R951-R952
12. Coyle S.M., Huntingford F.A., and Peichel C.L. Parallel evolution of Pitx1 underlies pelvic reduction in Scottish three-spined stickleback (Gasterosteus aculeatus). J. Hered. 98 (2007) 581-586
13. Bell M.A., Stewart J.D., and Park P.J. The world's oldest fossil threespine stickleback fish. Copeia 2009 (2009) 256-265
14. Nelson J.S. Absence of the pelvic complex in ninespine sticklebacks, Pungitius pungitius, collected in Ireland and Wood Buffalo National Park Region, Canada, with notes on meristic variation. Copeia 1971 (1971) 707-717
15. Bell M.A., Orti G., Walker J.A., and Koenings J.P. Evolution of pelvic reduction in threespine stickleback fish: a test of competing hypotheses. Evol. Int. J. Org. Evol. 47 (1993) 906-914
16. Chen T.-R., and Reisman H.M. A comparative chromosome study of the North American species of sticklebacks (Teleostei: Gasterosteidae). Cytogenetics 9 (1970) 321-332
17. Ocalewicz K., Fopp-Bay at D.F., Woznicki P., and Jankun M. Heteromorphic sex chromosomes in the ninespine stickleback Pungitius pungitius. J. Fish Biol. 73 (2008) 456-462
18. Ross J.A., Urton J.R., Boland J., Shapiro M.D., and Peichel C.L. Turnover of sex chromosomes in the stickleback fishes (Gasterosteidae). PLoS Genet 5 (2009) e1000391
19. Hunt G., Bell M.A., and Travis M.P. Evolution toward a new adaptive optimum: Phenotypic evolution in a fossil stickleback lineage. Evol. Int. J. Org. Evol. 62 (2008) 700-710
20. Blouw D.M., and Boyd G.J. Inheritance of reduction, loss, and asymmetry of the pelvis in Pungitius pungitius (ninespine stickleback). Heredity 68 (1992) 33-42
21. Giles N. The possible role of environmental calcium levels during the evolution of phenotypic diversity on Outer Hebridean populations of the three-spined stickleback, Gasterosteus aculeatus. J. Zool. 4 (1983) 535-544
22. Reimchen T.E. Spine deficiency and polymorphism in a population of Gasterosteus aculeatus: An adaptation to predators?. Can. J. Zool. 58 (1980) 1232-1244
23. Ziuganov V.V., and Zotin A.A. Pelvic girdle polymorphism and reproductive barriers in the ninespine stickleback Pungitius pungitius (L.) from northwest Russia. Behaviour 132 (1995) 1095-1105
24. Zyuganov V.V., and Rosanov A.S. Genetics of pelvic girdle reduction in fish (as illustrated by the ninespine stickleback Pungitius pungitius L.). Doklady Akademii Nauk SSR 293 (1987) 155-159
25. Marchinko K.B. Predation's role in repeated phenotypic and genetic divergence of armor in threespine stickleback. Evol. Int. J. Org. Evol. 63 (2009) 127-138
26. Shapiro M.D., Marks M.E., Peichel C.L., Nereng K., Blackman B.K., Jonsson B., Schluter D., and Kingsley D.M. Corrigendum: Genetic and developmental basis of evolutionary pelvic reduction in threespine sticklebacks. Nature 439 (2006) 1014
27. Szeto D.P., Rodriguez-Esteban C., Ryan A.K., O'Connell S.M., Liu F., Kioussi C., Gleiberman A.S., Izpisúa-Belmonte J.C., and Rosenfeld M.G. Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development. Genes Dev. 13 (1999) 484-494
28. Logan M., and Tabin C.J. Role of Pitx1 upstream of Tbx4 in specification of hindlimb identity. Science 283 (1999) 1736-1739
29. Shang J., Luo Y., and Clayton D.A. Backfoot is a novel homeobox gene expressed in the mesenchyme of developing hind limb. Dev. Dyn. 209 (1997) 242-253
30. Shapiro M.D., Bell M.A., and Kingsley D.M. Parallel genetic origins of pelvic reduction in vertebrates. Proc. Natl. Acad. Sci. USA 103 (2006) 13753-13758
31. Nelson J.S. Comparison of the pectoral and pelvic skeletons and of some other bones and their phylogenetic implications in the Aulorhynchidae and Gasterosteidae (Pisces). J. Fish. Res. Board Can. 28 (1971) 427-442
32. Bell M.A., Khalef V., and Travis M.P. Directional asymmetry of pelvic vestiges in threespine stickleback. J. Exp. Zoolog. B Mol. Dev. Evol. 308 (2007) 189-199
33. Marcil A., Dumontier E., Chamberland M., Camper S.A., and Drouin J. Pitx1 and Pitx2 are required for development of hindlimb buds. Development 130 (2003) 45-55
34. Gibson G., and Dworkin I. Uncovering cryptic genetic variation. Nat. Rev. Genet. 5 (2004) 681-690
35. Devlin R.H., and Nagahama Y. Sex determination and sex differentiation in fish: An overview of genetic, physiological, and environmental influences. Aquaculture 208 (2002) 191-364
36. Mank J.E., Promislow D.E., and Avise J.C. Evolution of alternative sex-determining mechanisms in teleost fishes. Biol. J. Linn. Soc. Lond. 87 (2006) 83-93
37. Woram R.A., Gharbi K., Sakamoto T., Hoyheim B., Holm L.E., Naish K., McGowan C., Ferguson M.M., Phillips R.B., Stein J., et al. Comparative genome analysis of the primary sex-determining locus in salmonid fishes. Genome Res. 13 (2003) 272-280
38. Chae B.S., and Yang H.J. Sexual dimorphism in eightspine stickleback, Pungitius sinensis: Gasterosteidae. Korean Journal of Zoology 33 (1990) 260-265
39. Kobayashi H. Cross-experiments with three species of stickleback, Pungitius pungitius (L.), Pungitius tymensis (Nikolsk), and Pungitius sinensis (Guichenot), with special reference to their systematic relationship. Journal of Hokkaido Gakugei University. Section B 10 (1959) 363-384
40. Kitano J., Mori S., and Peichel C.L. Sexual dimorphism in the external morphology of the threespine stickleback (Gasterosteus aculeatus). Copeia 2007 (2007) 336-349
41. Caldecutt W.J., and Adams D.C. Morphometrics of trophic osteology in the threespine stickleback, Gasterosteus aculeatus. Copeia 1998 (1998) 827-838
42. Caldecutt W.J., Bell M.A., and Buckland-Nicks J.A. Sexual dimorphism and geographic variation in dentition of threespine stickleback, Gasterosteus aculeatus. Copeia 2001 (2001) 936-944
43. McPhail J.D. Ecology and evolution of sympatric sticklebacks (Gasterosteus): evidence for a species-pair in Paxton Lake, Texada Island, British Columbia. Can. J. Zool. 70 (1992) 361-369
44. Albert A.Y., Sawaya S., Vines T.H., Knecht A.K., Miller C.T., Summers B.R., Balabhadra S., Kingsley D.M., and Schluter D. The genetics of adaptive shape shift in stickleback: pleiotropy and effect size. Evol. Int. J. Org. Evol. 62 (2008) 76-85
45. Aguirre W.E., Ellis K.E., Kusenda M., and Bell M.A. Phenotypic variation and sexual dimorphism in anadromous threespine stickleback: Implications for postglacial adaptive radiation. Biol. J. Linn. Soc. Lond. 95 (2008) 465-478
46. Charlesworth D., Charlesworth B., and Marais G. Steps in the evolution of heteromorphic sex chromosomes. Heredity 95 (2005) 118-128
47. Sucena E., Delon I., Jones I., Payre F., and Stern D.L. Regulatory evolution of shavenbaby/ovo underlies multiple cases of morphological parallelism. Nature 424 (2003) 935-938
48. Gompel N., Prud'homme B., Wittkopp P.J., Kassner V.A., and Carroll S.B. Chance caught on the wing: cis-regulatory evolution and the origin of pigment patterns in Drosophila. Nature 433 (2005) 481-487
49. Prud'homme B., Gompel N., Rokas A., Kassner V.A., Williams T.M., Yeh S.D., True J.R., and Carroll S.B. Repeated morphological evolution through cis-regulatory changes in a pleiotropic gene. Nature 440 (2006) 1050-1053
50. Davis G.K., Srinivasan D.G., Wittkopp P.J., and Stern D.L. The function and regulation of Ultrabithorax in the legs of Drosophila melanogaster. Dev. Biol. 308 (2007) 621-631
51. Hoekstra H.E. Genetics, development and evolution of adaptive pigmentation in vertebrates. Heredity 97 (2006) 222-234
52. Protas M., Conrad M., Gross J.B., Tabin C., and Borowsky R. Regressive evolution in the Mexican cave tetra, Astyanax mexicanus. Curr. Biol. 17 (2007) 452-454
53. Wilkens H. Genetic interpretation of regressive evolutionary process: Studies of hybrid eyes of two Astyanax cave populations (Characidae, Pisces). Evol. Int. J. Org. Evol. 25 (1971) 530-544
54. Borowsky R. Restoring sight in blind cavefish. Curr. Biol. 18 (2008) R23-R24
55. Hoekstra H.E., Hirschmann R.J., Bundey R.A., Insel P.A., and Crossland J.P. A single amino acid mutation contributes to adaptive beach mouse color pattern. Science 313 (2006) 101-104
56. Steiner C.C., Rompler H., Boettger L.M., Schoneberg T., and Hoekstra H.E. The genetic basis of phenotypic convergence in beach mice: Similar pigment patterns but different genes. Mol. Biol. Evol. 26 (2009) 35-45
57. Hoekstra H.E., and Nachman M.W. Different genes underlie adaptive melanism in different populations of rock pocket mice. Mol. Ecol. 12 (2003) 1185-1194
58. Wittkopp P.J., Williams B.L., Selegue J.E., and Carroll S.B. Drosophila pigmentation evolution: Divergent genotypes underlying convergent phenotypes. Proc. Natl. Acad. Sci. USA 100 (2003) 1808-1813
59. van Ooijen J.W. LOD significance thresholds for QTL analysis in experimental populations of diploid species. Heredity 83 (1999) 613-624