2011 William Allan Award: Development and Evolution1

American Journal of Human Genetics

Volumn 90, Issue 3, 2012, Pages 392-404

  Opitz, John M ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SONIC HEDGEHOG PROTEIN; TERATOGENIC AGENT;

ANATOMICAL CONCEPTS; ATAVISM; AUTOPSY; AWARDS AND PRIZES; CELL LINEAGE; CLINICAL PALEONTOLOGY; CONCEPT FORMATION; CONGENITAL MALFORMATION; DEVELOPMENTAL BIOLOGY; DEVELOPMENTAL FIELD THEORY; EMBRYO DEVELOPMENT; EMBRYO PATTERN FORMATION; EPIGENETICS; EVOLUTION; EVOLUTIONARY ADAPTATION; FIELD STUDY; GENE DUPLICATION; GENE EXPRESSION; GENE MUTATION; GENETIC VARIABILITY; GENOME; HISTOGENESIS; HUMAN; HUMAN DEVELOPMENT; LAST COMMON ANCESTOR; LUNG DEVELOPMENT; LUNG LOBE; MARSUPIAL; MEDICAL EDUCATION; MOLECULAR BIOLOGY; MORPHOGENESIS; NONHUMAN; NOTE; ONTOGENY; PALEONTOLOGY; PHENOTYPE; PHYLOGENY; PLACENTAL MAMMAL; PRIORITY JOURNAL; PROFESSIONAL COMPETENCE; PROTHERIAN; SIGNAL TRANSDUCTION; TETRAPLOIDY; THEORY; UROCHORDATA; ARTICLE; GROWTH, DEVELOPMENT AND AGING; MEDICAL GENETICS; MOLECULAR EVOLUTION;

AWARDS AND PRIZES; EVOLUTION, MOLECULAR; GENETICS, MEDICAL; GROWTH AND DEVELOPMENT; HUMANS;

EID: 84863751223     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.12.025     Document Type: Note

References (74)

1. Gilbert-Barness, E., Barness, L.A., In memoriam: John Lewis Emery (1915-2000). Pediatr. Dev. Pathol. 3 (2000), 509–512.
2. Bianchi, D.W., Fetomaternal cell trafficking: a new cause of disease?. Am. J. Med. Genet. 91 (2000), 22–28.
3. Witschi, E., Development of Vertebrates. 1956, WB Saunders, Philadelphia.
4. Huettner, A.F., Fundamentals of Comparative Embryology of the Vertebrates. Revised Edition, 1953, MacMillan, New York.
5. Witschi, E., Opitz, J.M., Fundamental aspects of intersexuality. Overzier, C., (eds.) Intersexuality, 1963, Academic Press, London, 16–34.
6. Barash, B.A., Freedman, L., Opitz, J.M., Anatomic studies in the 18-trisomy syndrome. Birth Defects Orig. Artic. Ser. 6 (1970), 3–15.
7. Spemann, H., Experimentelle Beiträge zu einer Theorie der Entwicklung. 1936, Julius Springer, Berlin.
8. Huxley, J.S., DeBeer, G.R., The Elements of Experimental Embryology. 1963, Hafner Publishing, New York.
9. Needham, J., Biochemistry and Morphogenesis. 1966, Harvard University Press, Cambridge, MA.
10. Oppenheimer, J.M., Essays in the History of Embryology and Biology. 1967, MIT Press, Cambridge, MA.
11. Stern, C., Two or three bristles. Am. Sci. 42 (1954), 213–247.
12. Opitz, J.M., Herrmann, J., Dieker, H., The study of malformation syndromes in man. Birth Defects Orig Artic Ser V(2) (1969), 1–10.
13. Spemann, H., Spemann's Nobel lecture: Les Prix Nobel en 1935. 1935, Imprim Roy., Norsted and Söner, Stockholm.
14. Meckel, J.F., Handbuch der pathologischen Anatomie, Volume 1, 1812, Reclam, Leipzig.
15. Darwin, C., The Origin of Species by Means of Natural Selection or the Preservation of Favored Races in the Struggle for Life. With Introduction and Bibliography by J.W. Burrow, Reprint of. First Edition, 1968, John Murray/Penguin Books, London.
16. Von Baer, K.E. (1828). Über Entwickelungsgeschichte der Thiere. Beobachtung und Reflexion Part I. (Königsberg: Borntrager).
17. Gilbert, S.F., Developmental biology. Ninth Edition, 2010, Sinauer, Sunderland, MA.
18. Davidson, E.H., The regulatory genome. 2006, AP/Elsevier, Amsterdam.
19. Capra, F., The science of Leonardo. 2007, Anchor/Random House, New York pp. 33.
20. Desmond, A., Archetypes and ancestors: Palaeontology in Victorian London. 1982, Blond and Briggs, London.
21. Fitch, W.M., Homology a personal view on some of the problems. Trends Genet. 16 (2000), 227–231.
22. Schlosser, G., Wagner, G.P., Modularity in Development and Evolution. 2004, University of Chicago Press, Chicago.
23. Davidson, E.H., Later embryogenesis: regulatory circuitry in morphogenetic fields. Development 118 (1993), 665–690.
24. Futuyama, D.J., Evolution. Second Edition, 2009, Sinauer Associates, Sunderland, MA.
25. Schatz, F., Klinische Beträge zur Physiologie des Fötus. 1990, August Hirschwald, Berlin.
26. Van Allen, M.I., Smith, D.W., Shepard, T.H., Twin reversed arterial perfusion (TRAP) sequence: a study of 14 twin pregnancies with acardius. Semin. Perinatol. 7 (1983), 285–293.
27. Hertwig, O., Lehrbuch der Entwicklungsgeschichte des Menschen und der Wirbelthiere. Fifth Edition, 1896, Gustav Fischer, Jena.
28. Whittaker, J.R., Chapter 18. Cephalochordates, the lancelets. Gilbert, S.F., Raunio, A.M., (eds.) Embryology: Constructing the Organism, 1997, Sinauer Associates, Sunderland, MA.
29. Holland, L.Z., Albalat, R., Azumi, K., Benito-Gutiérrez, E., Blow, M.J., Bronner-Fraser, M., Brunet, F., Butts, T., Candiani, S., Dishaw, L.J., et al. The amphioxus genome illuminates vertebrate origins and cephalochordate biology. Genome Res. 18 (2008), 1100–1111.
30. Yu, J.K., Meulemans, D., McKeown, S.J., Bronner-Fraser, M., Insights from the amphioxus genome on the origin of vertebrate neural crest. Genome Res. 18 (2008), 1127–1132.
31. Srivastava, M., Begovic, E., Chapman, J., Putnam, N.H., Hellsten, U., Kawashima, T., Kuo, A., Mitros, T., Salamov, A., Carpenter, M.L., et al. The Trichoplax genome and the nature of placozoans. Nature 454 (2008), 955–960.
32. Haecker, V., Entwicklungsgeschichtliche Eigenschafts - analyse. (Phänogenetik). 1918, Fischer, Jena.
33. Choe, S., Tanaka, A., Noguchi, T., Fujioka, S., Takatsuto, S., Ross, A.S., Tax, F.E., Yoshida, S., Feldmann, K.A., Lesions in the sterol delta reductase gene of Arabidopsis cause dwarfism due to a block in brassinosteroid biosynthesis. Plant J. 21 (2000), 431–443.
34. Kelley, R.L., Roessler, E., Hennekam, R.C.M., Feldman, G.L., Kosaki, K., Jones, M.C., Palumbos, J.C., Muenke, M., Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?. Am. J. Med. Genet. 66 (1996), 478–484.
35. Porter, J.A., Young, K.E., Beachy, P.A., Cholesterol modification of hedgehog signaling proteins in animal development. Science 274 (1996), 255–259.
36. Chiang, C., Litingtung, Y., Lee, E., Young, K.E., Corden, J.L., Westphal, H., Beachy, P.A., Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function. Nature 383 (1996), 407–413.
37. Desmond, E., Gribaldo, S., Phylogenomics of sterol synthesis: insights into the origin, evolution, and diversity of a key eukaryotic feature. Genome Biol Evol 1 (2009), 364–381.
38. Lingwood, D., Simons, K., Lipid rafts as a membrane-organizing principle. Science 327 (2010), 46–50.
39. Pallister, P.D., Opitz, J.M., The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafness. Am. J. Med. Genet. 4 (1979), 239–246.
40. Pierce, S.B., Chisholm, K.M., Lynch, E.D., Lee, M.K., Walsh, T., Opitz, J.M., Li, W., Klevit, R.E., King, M.C., Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc. Natl. Acad. Sci. USA 108 (2011), 6543–6548.
41. Forterre, P., Philippe, H., The last universal common ancestor (LUCA), simple or complex?. Biol. Bull. 196 (1999), 373–375 discussion 375–377.
42. Woese, C., The universal ancestor. Proc. Natl. Acad. Sci. USA 95 (1998), 6854–6859.
43. Theobald, D.L., A formal test of the theory of universal common ancestry. Nature 465 (2010), 219–222.
44. Morange, M., Some considerations on the nature of LUCA, and the nature of life. Res. Microbiol. 162 (2011), 5–9.
45. Moreira, D., López-García, P., Ten reasons to exclude viruses from the tree of life. Nat. Rev. Microbiol. 7 (2009), 306–311.
46. Di Giulio, M., The last universal common ancestor (LUCA) and the ancestors of archaea and bacteria were progenotes. J. Mol. Evol. 72 (2011), 119–126.
47. Glansdorff, N., Xu, Y., Labedan, B., The last universal common ancestor: emergence, constitution and genetic legacy of an elusive forerunner. Biol. Direct, 3, 2008, 29.
48. Forterre, P., Gribaldo, S., Brochier, C., Luca: À la recherche du plus proche ancêtre commun universel. Med. Sci. 21 (2005), 860–865.
49. Becerra, A., Delaye, L., Islas, S., Lazcano, A., The very early stages of biological evolution and the nature of the last common ancestor of the three major cell domains. Annu. Rev. Ecol. Evol. Syst. 38 (2007), 361–379.
50. Hoenigsberg, H., Evolution without speciation but with selection: LUCA, the Last Universal Common Ancestor in Gilbert's RNA world. Genet. Mol. Res. 2 (2003), 366–375.
51. Doolittle, W.F., Uprooting the tree of life. Sci. Am. 282 (2000), 90–95.
52. Creevey, C.J., Doerks, T., Fitzpatrick, D.A., Raes, J., Bork, P., Universally distributed single-copy genes indicate a constant rate of horizontal transfer. PLoS ONE, 6, 2011, e22099 Published online Aug 5, 2011.
53. Tuller, T., Birin, H., Gophna, U., Kupiec, M., Ruppin, E., Reconstructing ancestral gene content by coevolution. Genome Res. 20 (2010), 122–132.
54. Mushegian, A., Gene content of LUCA, the last universal common ancestor. Front. Biosci. 13 (2008), 4657–4666.
55. Mat, W.K., Xue, H., Wong, J.T.F., The genomics of LUCA. Front. Biosci. 13 (2008), 5605–5613.
56. Ouzounis, C.A., Kunin, V., Darzentas, N., Goldovsky, L., A minimal estimate for the gene content of the last universal common ancestor—exobiology from a terrestrial perspective. Res. Microbiol. 157 (2006), 57–68.
57. Ranea, J.A.G., Sillero, A., Thornton, J.M., Orengo, C.A., Protein superfamily evolution and the last universal common ancestor (LUCA). J. Mol. Evol. 63 (2006), 513–525.
58. Sobolevsky, Y., Trifonov, E.N., Protein modules conserved since LUCA. J. Mol. Evol. 63 (2006), 622–634.
59. David, L.A., Alm, E.J., Rapid evolutionary innovation during an Archaean genetic expansion. Nature 469 (2011), 93–96.
60. Haeckel, E., Anthropogenie oder Entwickelungsgeschichte des Menschen: gemeinverständliche wissenschaftliche Vorträge über die Grundzüge der menschlichen Keimes- und Stammesgeschichte. 1874, Wilhelm Engelmann, Leipzig, Germany.
61. Gould, S.J., Ontogeny and phylogeny. 1977, Belknap/Harvard Univ Press, Cambridge, MA.
62. Sander, K., The evolution of patterning mechanisms. Gleanings from insect embryogenesis and spermatogenesis. Goodwin, B.C., Holder, N., Wylie, C.C., (eds.) Development and Evolution, 1983, Cambridge University Press, Cambridge, 137–159.
63. Kalinka, A.T., Varga, K.M., Gerrard, D.T., Preibisch, S., Corcoran, D.L., Jarrells, J., Ohler, U., Bergman, C.M., Tomancak, P., Gene expression divergence recapitulates the developmental hourglass model. Nature 468 (2010), 811–814.
64. Domazet-Lošo, T., Tautz, D., A phylogenetically based transcriptome age index mirrors ontogenetic divergence patterns. Nature 468 (2010), 815–818.
65. Prud'homme, B., Gompel, N., Evolutionary biology: Genomic hourglass. Nature 468 (2010), 768–769.
66. Haldane, J.B.S., The nature of interspecific differences. DeBeer, G.R., (eds.) Evolution, Essays on aspects of evolutionary biology, 1938, Clarendom Press, Oxford, 79–94.
67. Ohno, S., Evolution by gene duplication. 1970, Springer, Berlin.
68. Furlong, R.F., Holland, P.W.H., Were vertebrates octoploid?. Philos. Trans. R. Soc. Lond. B Biol. Sci. 357 (2002), 531–544.
69. Putnam, N.H., Butts, T., Ferrier, D.E.K., Furlong, R.F., Hellsten, U., Kawashima, T., Robinson-Rechavi, M., Shoguchi, E., Terry, A., Yu, J.K., et al. The amphioxus genome and the evolution of the chordate karyotype. Nature 453 (2008), 1064–1071.
70. Gilbert, E.F., Dawson, G., zu Rhein, G.M., Opitz, J.M., Spranger, I-cell disease, mucolipidosis II. Pathological, histochemical, ultrastructural and biochemical observations in four cases. Z. Kinderheilkd. 114 (1973), 259–292.
71. Opitz, J.M., Development: clinical and evolutionary considerations. Am. J. Med. Genet. A. 143A (2007), 2853–2861.
72. Arch d'Anat microscop et de Morphol Expérim. 48(2): Jubilé scientif. du Prof Emil Witschi.
73. Haeckel, E., Art Forms from the Ocean: The Radiolarian Atlas of 1862. 2005, Prestel Verlag, Munich.
74. Hinrichsen, K.V., (eds.) Humanembryologie, 1990, Springer, Berlin.