Expression of reelin, the gene responsible for the reeler mutation, in embryonic development and adulthood in the mouse

Developmental Dynamics

Volumn 210, Issue 2, 1997, Pages 157-172

  Ikeda, Yayoi ^a   Terashima, Toshio ^a  

^a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

Author keywords

Cajal Retzius cells; In situ hybridization; reeler mutant mouse; reelin

Indexed keywords

ADOLESCENT; ANIMAL TISSUE; ARTICLE; BRAIN; CELL MIGRATION; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; GENE MUTATION; IN SITU HYBRIDIZATION; MOUSE; NEUROECTODERM; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SOMITE; SPINAL CORD; TISSUE DISTRIBUTION; YOLK SAC;

ANIMALS; BRAIN; CELL ADHESION MOLECULES, NEURONAL; EXTRACELLULAR MATRIX PROTEINS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IN SITU HYBRIDIZATION; MICE; MICE, NEUROLOGIC MUTANTS; NERVE TISSUE PROTEINS; PHENOTYPE; SERINE ENDOPEPTIDASES;

ANIMALIA;

EID: 0030848528     PISSN: 10588388     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0177(199710)210:2<157::AID-AJA8>3.0.CO;2-F     Document Type: Article

References (25)

1. Bar I, Lambert de Rouvroit C, Royaux I, Krizman DB, Dernoncourt C, Ruelle D, Beckers MC, Goffinet AF. A YAC contig containing the reeler locus with preliminary characterization of candidate gene fragments. Genomics 1995;26:543-549.
2. Caviness VS Jr, Crandall JE, Edwards MA. The reeler malformation. Implications for neocortical development: A view from mutations in mice. In: Peters A, Jones EG, eds. Cerebral Cortex. Volume 7. Development and Maturation of Cerebral Cortex. New York: Plenum Press, 1990;59-89.
3. D'Arcangelo G, Miao GG, Chen S-C, Soares HD, Morgan JI, Curran T. A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 1995;374:719-723.
4. D'Arcangelo G, Nakajima K, Miyata T, Ogawa M, Mikoshiba K, Curran T. Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody. J Neurosci 1997;17:23-31.
5. Del Río JA, Heimrich B, Borrel V, Forster E, Drakew A, Alcantara S, Nakajima K, Miyata T, Ogawa M, Mikoshiba K, Derer O, Frotscher M, Soriano E. A role for Cajal-Retzius cells and reelin in the development of hippocampal connections. Nature 1997;385:70-74.
6. Derer P, Derer M. Cajal-Retzius cells ontogenesis and death in mouse brain visualized with horseradish peroxidase and electron microscopy. Neuroscience 1990;36:839-856.
7. Falconer DS. Two new mutations, trembler and reeler with neurological action in the mouse. J Genet 1951;50:192-201.
8. Ghosh A. Axons follow Reelin routes. Nature 1997;385:23-24.
9. Goffinet AM. Events governing the organization of postmigratory neurons: Studies on brain developing in normal and reeler mouse. Brain Res Rev 1984;7:261-296.
10. Goffinet AM. Determinants of nerve cell patterns during development: a review. Eur J Morphol 1990;28:149-168.
11. Hirotsune S, Takahara T, Sasaki N, Hirose K, Yoshiki A, Ohashi T, Kusakabe M, Murakami Y, Muramatsu M, Watanabe S, Nakao K, Katsuki M, Hayashizaki Y. The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons. Nature Genet 1995;10: 77-83.
12. Kaufman MH. The Atlas of Mouse Development. Kaufman MH, ed. London: Academic Press, 1992.
13. Miettinen M, Pitkänen A, Miettinen R. Distribution of Calretinin-immunoreactivity in the rat entorhinal cortex: Coexistence with GABA. J Comp Neurol 1997;378:363-378.
14. Miyata T, Nakajima K, Aruga J, Takahashi S, Ikenaka K, Mikoshiba K, Ogawa M. Distribution of the reelin gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogenic antibody CR-50 on normal and reeler mice. J Comp Neurol 1996;372:215-228.
15. Ogawa M, Miyata T, Nakajima K, Yagyu K, Seike M, Ikenaka K, Yamamoto H, and Mikoshiba K. The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons. Neuron 1995;14:899-912.
16. Rakic P, Caviness VS Jr. Cortical development: View from neurological mutants two decades later. Neuron 1995;14:1101-1104.
17. Rosati R, Horan G, Pinero GJ, Garofalo S, Keene DR, Hoton WA, Vuorio E, de Crombrugghe B, and Behringer RR. Normal long bone growth and development in type X collagen-null mice. Nature Genet 1994;8:129-135.
18. Rudniki MA, Braun T, Hinuma S, Jaenisch R. Inactivation of myoD in mice leads to up-regulation of the myogenic HLH gene myf-5 and results in apparently normal muscle development. Cell 1992;71:383-390.
19. Saga Y, Yagi T, Ikawa Y, Sakakura T, and Aizawa S. Mice develop normally without tenascin. Genes Dev 1992;6:1821-1831.
20. Soriano E, Del Río JA, Martinez A, Super H. Organization of the embryonic and early postnatal murine hippocampus. I. Immunocytochemical characterization of neuronal populations in the subplate and marginal zone. J Comp Neurol 1994;342:571-595.
21. Sweet HO, Bronson RT, Johnson KR, Cook SA, Davisson MT. Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration. Mammal Genome 1996;7:798-802.
22. Terashima T. Anatomy, development and lesion-induced plasticity of rodent corticospinal tract. Neurosci Res 1995;22:139-161.
23. Wilkinson DG. In situ hybridization. In: Stern CD, Holland PWH, eds. Essential Developmental Biology: A Practical Approach. Oxford: IRL Press, 1993;257-274.
24. Wyss JM, Stanfield BB, Cowan WM. Structural abnormalities in the olfactory bulb of the reeler mouse. Brain Res 1980;188:566-571.
25. Zhou F-H, Hablitz JJ. Morphological properties of intracellulary labeled layer I neurons in rat neocortex. J Comp Neurol 1996;376: 198-213.