The role of FGF-3 in early inner ear development: An analysis in normal and kreisler mutant mice

Developmental Biology

Volumn 174, Issue 2, 1996, Pages 370-378

  McKay, Ian J ^a   Lewis, Julian ^b   Lumsden, Andrew ^a  

^a GUY S HOSPITAL   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR 3;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; EAR DEVELOPMENT; EMBRYO; GENE EXPRESSION; INNER EAR; MOUSE; MUTANT; NONHUMAN; PRIORITY JOURNAL; TISSUE DIFFERENTIATION;

ANIMALIA;

EID: 0030005799     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1996.0081     Document Type: Article

References (31)

1. Carney, P. R., and Couvé, E. (1989). Cell polarity changes and migration during early development of the avian peripheral auditory system. Anat. Rec. 225, 156-164.
2. Carney, P. R., and Silver, J. (1983). Studies on cell migration and axon guidance in the developing distal auditory system of the mouse. J. Comp. Neurol. 215, 359-369.
3. Carpenter, E. M., Goddard, T. M., Chisaka, O., Manley, N. R., and Cappecchi, M. R. (1993). Loss of Hox-A1 (Hox 1.6) function results in the reorganization of the murine hindbrain. Development 118, 1063-1075.
4. Chisaka, O., Musci, T. S., and Capecchi, M. R. (1992). Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6. Nature 355, 516-520.
5. Cordes, S. P., and Barsh, G. S. (1994). The mouse segmentation gene kr encodes a novel basic domain-leucine zipper transcription factor. Cell 79, 1025-1034.
6. D'Amico-Martel, A., and Noden, D. M. (1983). Contributions of placodal and neural crest cells to avian cranial ganglia. Am. J. Anat. 166, 445-468.
7. Deol, M. S. (1964). The abnormalities of the inner ear in kreisler mice. J. Embryol. Exp. Morphol. 12, 475-490.
8. Detwiler, S. R., and Van Dyke, R. H. (1950). The role of the medulla in the differentiation of the otic vesicle. J. Exp. Zool. 113, 179-199.
9. Dickson, C., Deed, R., Dixon, M., and Peters, G. (1989). The structure and function of the int-2 oncogene. Prog. Growth Factor Res. 1, 123-132.
10. Dollé, P., Lufkin, T., Krumlauf, R., Mark, M., Duboule, D., and Chambon, P. (1993). Local alterations of Krox-20 and Hox gene expression in the hindbrain suggest lack of rhombomeres 4 and 5 in homozygote null Hoxa-1 (Hox-1.6) mutant embryos. Proc. Natl. Acad. Sci. USA 90, 7666-7670.
11. Frohman, M. A., Martin, G. R., Cordes, S. P., Halamek, L. P., and Barsh, G. S. (1993). Altered rhombomere-specific gene expression and hyoid bone differentiation in the mouse segmentation mutant kreisler (kr). Development 117, 925-936.
12. Gospodarowicz, D., Ferrara, N., Schweigerer, L., and Neufeld, G. (1987). Structural characterisation and biological functions of fibroblast growth factor. Endocr. Rev. 8, 95-114.
13. Harrison, R. G. (1935). Factors concerned in the development of the ear in Amblystoma punctatum. Anat. Rec. 64(Suppl. 1), 38-39.
14. Hertwig, P. (1944). Die Genese der Hirn-und Gehörorganm ißbildungen bei röntgenmutierten Kreislermäusen. Z. KonstLehnre 28, 327-354.
15. Jacobson, A. G. (1966). Inductive processes in embryonic development. Science 152, 25-34.
16. Lufkin, T., Dierich, A., Lemeur, M., Mark, M., and Chambon, P. (1991). Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression. Cell 66, 1105-1120.
17. Lyon, M. F., and Searle, A. G. (1990). "Genetic Variants and Strains of the Laboratory Mouse." Oxford Univ. Press, Oxford/Fischer, Stuttgart.
18. Mahmood, R., Keifer, P., Guthrie, S., Dickson, C., and Mason, I. (1995). Multiple roles for FGF-3 during cranial neural development in the chicken. Development 121, 1399-1410.
19. Mansour, S. L., and Martin, G. R. (1988). Four classes of mRNA are expressed from the mouse int-2 gene, a member of the FGF gene family. EMBO J. 7, 2035-2041.
20. Mansour, S. L., Goddard, J. M., and Capecchi, M. R. (1993). Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear. Development 117, 13-28.
21. Mark, M., Lufkin, T., Vonesch, J.-L., Ruberté, E., Oliver, J.-C., Dollé, P., Gorry, P., Lumsden, A., and Chambon, P. (1993). Two rhombomeres are altered in Hoxa-1 mutant mice. Development 119, 319-338.
22. McKay, I. J., Muchamore, I., Krumlauf, R., Maden, M., Lumsden, A., and Lewis, J. (1994). The kreisler mouse, a hindbrain segmentation mutant that lacks two rhombomeres. Development 120, 2199-2211.
23. Moore, R., Casey, G., Brookes, S., Dixon, M., Peters, G., and Dickson, C. (1986). Sequence topography and protein coding potential of mouse int-2: A putative oncogene activated by mouse mammary tumour virus. EMBO J. 5, 919-924.
24. Represa, J., León, Y., Miner, C., and Giraldez, F. (1991). The int-2 proto-oncogene is responsible for induction of the inner ear. Nature 353, 561-563.
25. Ruben, R. J. (1973). Development and cell kinetics of the kreisler (kr/kr) mouse. Laryngoscope 83, 1440-1468.
26. Stone, L. S. (1931). Induction of the ear by the medulla and its relation to experiments on the lateralis system in amphibia. Science 14, 577.
27. Wilkinson, D. G. (1992). Wholemount in situ hybridization of vertebrate embryos. In "In Situ Hybridization" (D. G. Wilkinson, Ed.). IRL Press, Oxford.
28. Wilkinson, D. G., and Green, J. (1991). In situ hybridization. In "Postimplantation Mammalian Embryos. The Practical Approach" (A. J. Copp and D. L. Cockcroft, Eds.), pp. 155-167. IRL Press, Oxford.
29. Wilkinson, D. G., Bhatt, S., and McMahon, A. P. (1989). Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development. Development 105, 131-136.
30. Wilkinson, D. G., Peters, G., Dickson, C., and McMahon, A. P. (1988). Expression of the FGF-related proto-oncogene int-2 during gastrulation and neurulation in the mouse. EMBO J. 7, 691-695.
31. Yntema, G. L. (1955). Ear and nose. In "Analysis of Development," pp. 415-428. Saunders, Philadelphia/London.