Leaning to the left: Laterality in the zebrafish forebrain

Trends in Neurosciences

Volumn 26, Issue 6, 2003, Pages 308-313

  Halpern, Marnie E ^a   Liang, Jennifer O ^a,b   Gamse, Joshua T ^a  

^a GEOPHYSICAL LABORATORY   (United States)

^b CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN; BRAIN DEVELOPMENT; DIENCEPHALON; EPITHALAMUS; FOREBRAIN; GENETICS; HABENULA; HEMISPHERIC DOMINANCE; MORPHOLOGY; NONHUMAN; PINEAL BODY; PRIORITY JOURNAL; REVIEW; SIGNAL TRANSDUCTION; VERTEBRATE; VISCERA; ZEBRA FISH;

EID: 0037533817     PISSN: 01662236     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0166-2236(03)00129-2     Document Type: Review

References (79)

1. Petty R.G. Structural asymmetries of the human brain and their disturbance in schizophrenia. Schizophr. Bull. 25:1999;121-139.
2. Steffens D.C., Krishnan K.R.R. Structural neuroimaging and mood disorders: recent findings, implications for classification, and future directions. Biol. Psychiatry. 43:1998;705-712.
3. Pujol J., et al. CSF spaces of the Sylvian fissure region in severe melancholic depression. NeuroImage. 15:2002;103-106.
4. Hendren R.L., et al. Review of neuroimaging studies of child and adolescent psychiatric disorders from the past 10 years. J. Am. Acad. Child Adolesc. Psychiatry. 39:2000;815-828.
5. Herbert M.R., et al. Abnormal asymmetry in language association cortex in autism. Ann. Neurol. 52:2002;588-596.
6. Robichon F., et al. Developmental dyslexia: atypical cortical asymmetries and functional significance. Eur. J. Neurol. 7:2000;35-46.
7. Morgan A.E., Hynd G.W. Dyslexia, neurolinguistic ability, and anatomical variation of the planum temporale. Neuropsychol. Rev. 8:1998;79-93.
8. Changeux J.-P. Neuronal Man: The Biology of Mind. 1985;Pantheon Books, New York.
9. McManus C. Right Hand, Left Hand: The Origins of Asymmetry In Brains, Bodies, Atoms and Cultures. 2002;Harvard University Press.
10. Geschwind N., Levitsky W. Human brain: left-right asymmetries in temporal speech region. Science. 161:1968;186-187.
11. Galaburda A.M., et al. Right-left asymmetries in the brain. Science. 199:1978;852-856.
12. LeMay M. Morphological aspects of human brain asymmetry: an evolutionary perspective. Trends Neurosci. 5:1982;273-275.
13. LeMay M. Functional and anatomical asymmetries of the human brain. Eur. J. Neurol. 6:1999;79-85.
14. Toga A.W., Thompson P.M. Mapping brain asymmetry. Nat. Rev. Neurosci. 4:2003;37-48.
15. Hopkins W.D., et al. Planum temporale asymmetries in great apes as revealed by magnetic resonance imaging (MRI). NeuroReport. 9:1998;2913-2918.
16. Gannon P.J., et al. Asymmetry of chimpanzee planum temporale: humanlike pattern of Wernicke's brain language area homolog. Science. 279:1998;220-222.
17. Suthers R.A. Peripheral control and lateralization of birdsong. J. Neurobiol. 33:1997;632-652.
18. Ehret G. Left hemisphere advantage in the mouse brain for recognizing ultrasonic communication calls. Nature. 325:1987;249-251.
19. Bisazza A., et al. The origins of cerebral asymmetry: a review of evidence of behavioural and brain lateralization in fishes, reptiles and amphibians. Neurosci. Biobehav. Rev. 22:1998;411-426.
20. Corballis M.C. Cerebral asymmetry: motoring on. Trends Cogn. Sci. 2:1998;152-157.
21. Wiltschko W., et al. Lateralization of magnetic compass orientation in a migratory bird. Nature. 419:2002;467-470.
22. Rogers L.J. Evolution of hemispheric specialization: advantages and disadvantages. Brain Lang. 73:2000;236-253.
23. Rogers L.J., Andrew R.J. Comparative Vertebrate Lateralization. 2002;Cambridge University Press.
24. Hamada H., et al. Establishment of vertebrate left-right asymmetry. Nat. Rev. Genet. 3:2002;103-113.
25. Wright C.V., Halpern M.E. Specification of left-right asymmetry. Results Probl. Cell Differ. 40:2002;96-116.
26. Harris J.A., et al. Diencephalic asymmetries. Neurosci. Biobehav. Rev. 20:1996;637-643.
27. Braitenberg V., Kemali M. Exceptions to bilateral symmetry in the epithalamus of lower vertebrates. J. Comp. Neurol. 138:1970;137-146.
28. Concha M.L., Wilson S.W. Asymmetry in the epithalamus of vertebrates. J. Anat. 199:2001;63-84.
29. Butler A.B., Hodos W. Comparative Vertebrate Neuroanatomy: Evolution and Adaptation. 1996;Wiley-Liss.
30. Borg B., et al. The parapineal organ of teleosts. Acta Zool. 64:1983;211-218.
31. van Veen T., et al. The pineal complex of the three-spined stickleback, Gasterosteus aculeatus L. a light-, electron microscopic and fluorescence histochemical investigation. Cell Tissue Res. 209:1980;11-28.
32. Yanez J., Anadon R. Afferent and efferent connections of the habenula in the larval sea lamprey (Petromyzon marinus L.): an experimental study. J. Comp. Neurol. 345:1994;148-160.
33. Yanez J., Anadon R. Afferent and efferent connections of the habenula in the rainbow trout (Oncorhynchus mykiss): an indocarbocyanine dye (DiI) study. J. Comp. Neurol. 372:1996;529-543.
34. Hokfelt T., et al. In memory of Milena Kemali: the scientist, the person. Neurosci. Biobehav. Rev. 20:1996;555-556.
35. Kemali M., Guglielmotti V. An electron microscope observation of the right and the two left portions of the habenular nuclei of the frog. J. Comp. Neurol. 176:1977;133-148.
36. Kemali M., Guglielmotti V. Quantitative evaluation of the number of fibers in the right and left fasciculus retroflexus using horseradish peroxidase. Z. Mikrosk. Anat. Forsch. 96:1982;750-754.
37. Morgan M.J., et al. Development of left-right asymmetry in the habenular nuclei of Rana temporaria. J. Comp. Neurol. 149:1973;203-214.
38. Guglielmotti V., Fiorino L. Nitric oxide synthase activity reveals an asymmetrical organization of the frog habenulae during development: a histochemical and cytoarchitectonic study from tadpoles to the mature Rana esculenta, with notes on the pineal complex. J. Comp. Neurol. 411:1999;441-454.
39. Wehrmaker A. Right-left asymmetry and situs inversus in Triturus alpestris. Wilhelm Roux's Arch. Dev. Biol. 163:1969;1-32.
40. Sutherland R.J. The dorsal diencephalic conduction system: a review of the anatomy and functions of the habenular complex. Neurosci. Biobehav. Rev. 6:1982;1-13.
41. Sandyk R. Relevance of the habenular complex to neuropsychiatry: a review and hypothesis. Int. J. Neurosci. 61:1991;189-219.
42. Gurusinghe C.J., Ehrlich D. Sex-dependent structural asymmetry of the medial habenular nucleus of the chicken brain. Cell Tissue Res. 240:1985;149-152.
43. Gurusinghe C.J., et al. The influence of testosterone on the sex-dependent structural asymmetry of the medial habenular nucleus of the chicken. J. Comp. Neurol. 253:1986;153-162.
44. Kemali M., et al. The asymmetry of the habenular nuclei of female and male frogs in spring and winter. Brain Res. 517:1990;251-255.
45. Sampath K., et al. Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling. Nature. 395:1998;185-189.
46. Rebagliati M.R., et al. Zebrafish nodal-related genes are implicated in axial patterning and establishing left-right asymmetry. Dev. Biol. 199:1998;261-272.
47. Rebagliati M.R., et al. cyclops encodes a nodal-related factor involved in midline signaling. Proc. Natl. Acad. Sci. U. S. A. 95:1998;9932-9937.
48. Thisse C., Thisse B. Antivin, a novel and divergent member of the TGFβ superfamily, negatively regulates mesoderm induction. Development. 126:1999;229-240.
49. Liang J.O., et al. Asymmetric nodal signaling in the zebrafish diencephalon positions the pineal organ. Development. 127:2000;5101-5112.
50. Essner J.J., et al. Mesendoderm and left-right brain, heart and gut development are differentially regulated by pitx2 isoforms. Development. 127:2000;1081-1093.
51. Bisgrove B.W., et al. Multiple pathways in the midline regulate concordant brain, heart and gut left-right asymmetry. Development. 127:2000;3567-3579.
52. Conlon F.L., et al. A primary requirement for nodal in the formation and maintenance of the primitive streak in the mouse. Development. 120:1994;1919-1928.
53. Zhou X., et al. Nodal is a novel TGF-β-like gene expressed in the mouse node during gastrulation. Nature. 361:1993;543-547.
54. Collignon J., et al. Relationship between asymmetric nodal expression and the direction of embryonic turning. Nature. 381:1996;155-158.
55. Boorman C., Shimeld S.M. The evolution of left-right asymmetry of chordates. BioEssays. 24:2002;1004-1011.
56. Gritsman K., et al. The EGF-CFC protein One-eyed pinhead is essential for nodal signaling. Cell. 97:1999;121-132.
57. Pogoda H.M., et al. The zebrafish forkhead transcription factor FoxH1/Fast1 is a modulator of nodal signaling required for organizer formation. Curr. Biol. 10:2000;1041-1049.
58. Sirotkin H.I., et al. Fast1 is required for the development of dorsal axial structures in zebrafish. Curr. Biol. 10:2000;1051-1054.
59. Gothilf Y., et al. Zebrafish serotonin N-acetyltransferase-2: marker for development of pineal photoreceptors and circadian clock function. Endocrinology. 140:1999;4895-4903.
60. Concha M.L., et al. A nodal signaling pathway regulates the laterality of neuroanatomical asymmetries in the zebrafish forebrain. Neuron. 28:2000;399-409.
61. Gamse J.T., et al. Otx5 regulates genes that show circadian expression in the zebrafish pineal complex. Nat. Genet. 30:2002;117-121.
62. Gamse J.T., et al. The parapineal mediates left-right asymmetry in the zebrafish diencephalon. Development. 130:2003;1059-1068.
63. Papazian D.M. Potassium channels: some assembly required. Neuron. 23:1999;7-10.
64. +-ATPase and cell membrane potentials comprise a very early step in left-right patterning. Cell. 111:2002;77-89.
65. Essner J.J., et al. Conserved function for embryonic nodal cilia. Nature. 418:2002;37-38.
66. Yan Y.T., et al. Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation. Genes Dev. 13:1999;2527-2537.
67. Braford M.R., Northcutt R.G. Organization of the Diencephalons and Pretectum of the Ray-Finned Fishes. Vol. 2:1983;University of Michigan Press.
68. Haffter P., et al. The identification of genes with unique and essential functions in the development of the zebrafish Danio rerio. Development. 123:1996;1-36.
69. Moens C.B., Fritz A. Techniques in neural development. Methods Cell Biol. 59:1999;253-272.
70. Miklosi A., Andrew R.J. Right eye use associated with decision to bite in zebrafish. Behav. Brain Res. 105:1999;199-205.
71. Miklosi A., et al. Role of right hemifield in visual control of approach to target in zebrafish. Behav. Brain Res. 122:2001;57-65.
72. Sovrano V.A., et al. Lateralization of response to social stimuli in fishes: a comparison between different methods and species. Physiol. Behav. 74:2001;237-244.
73. Bisazza A., et al. Population lateralisation and social behaviour: a study with 16 species of fish. Laterality. 5:2000;269-284.
74. Heuts B.A. Lateralization of trunk muscle volume, and lateralization of swimming turns of fish responding to external stimuli. Behav. Processes. 47:1999;113-124.
75. Koshiba M., et al. Light-dependent development of asymmetry in the ipsilateral and contralateral thalamofugal visual projections of the chick. Neurosci. Lett. 336:2003;81-84.
76. Gerendai I., Halász B. Neuroendocrine asymmetry. Front. Neuroendocrinol. 18:1997;354-381.
77. Ifthikharuddin S.F., et al. MR volumetric analysis of the human basal ganglia: normative data. Acad. Radiol. 7:2000;627-634.
78. Geschwind D.H., et al. Molecular approaches to cerebral laterality: development and neurodegeneration. Am. J. Med. Genet. 101:2001;370-381.
79. Masai I., et al. floating head and masterblind regulate neuronal patterning in the roof of the forebrain. Neuron. 18:1997;43-57.