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JOURNAL ARTICLES
Otx1 and Otx2 activities are required for the normal development of the mouse inner ear
H. Morsli, F. Tuorto, D. Choo, M.P. Postiglione, A. Simeone, D.K. Wu
Development 1999 126: 2335-2343;
H. Morsli
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F. Tuorto
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D. Choo
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M.P. Postiglione
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A. Simeone
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D.K. Wu
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Summary

The Otx1 and Otx2 genes are two murine orthologues of the Orthodenticle (Otd) gene in Drosophila. In the developing mouse embryo, both Otx genes are expressed in the rostral head region and in certain sense organs such as the inner ear. Previous studies have shown that mice lacking Otx1 display abnormal patterning of the brain, whereas embryos lacking Otx2 develop without heads. In this study, we examined, at different developmental stages, the inner ears of mice lacking both Otx1 and Otx2 genes. In wild-type inner ears, Otx1, but not Otx2, was expressed in the lateral canal and ampulla, as well as part of the utricle. Ventral to the mid-level of the presumptive utricle, Otx1 and Otx2 were co-expressed, in regions such as the saccule and cochlea. Paint-filled membranous labyrinths of Otx1−/− mutants showed an absence of the lateral semicircular canal, lateral ampulla, utriculosaccular duct and cochleosaccular duct, and a poorly defined hook (the proximal part) of the cochlea. Defects in the shape of the saccule and cochlea were variable in Otx1−/− mice and were much more severe in an Otx1−/−;Otx2(+/)- background. Histological and in situ hybridization experiments of both Otx1−/− and Otx1−/−;Otx2(+/)- mutants revealed that the lateral crista was absent. In addition, the maculae of the utricle and saccule were partially fused. In mutant mice in which both copies of the Otx1 gene were replaced with a human Otx2 cDNA (hOtx2(1)/ hOtx2(1)), most of the defects associated with Otx1−/− mutants were rescued. However, within the inner ear, hOtx2 expression failed to rescue the lateral canal and ampulla phenotypes, and only variable rescues were observed in regions where both Otx1 and Otx2 are normally expressed. These results suggest that both Otx genes play important and differing roles in the morphogenesis of the mouse inner ear and the development of its sensory organs.

Reference

    1. Acampora D.,
    2. Avantaggiato V.,
    3. Tuorto F.,
    4. Barone P.,
    5. Perera M.,
    6. Choo D.,
    7. Wu D.,
    8. Corte G.,
    9. Simeone A.
    (1999) Differential transcriptional control as the major molecular event in generating Otx1/ and Otx2/ divergent phenotypes. Development 126, 1417–1426
    OpenUrlAbstract
    1. Acampora D.,
    2. Avantaggiato V.,
    3. Tuorto F.,
    4. Barone P.,
    5. Reichert H.,
    6. Finkelstein R.,
    7. Simeone A.
    (1998) Murine Otx1 and Drosophila otd genes share conserved genetic functions required in invertebrate and vertebrate brain development. Development 125, 1691–1702
    OpenUrlAbstract
    1. Acampora D.,
    2. Avantaggiato V.,
    3. Tuorto F.,
    4. Briata P.,
    5. Corte G.,
    6. Simeone A.
    (1998) Visceral endoderm-restricted translation of Otx1 mediates recovering of Otx2 requirements for specification of anterior neural plate and proper gastrulation. Development 125, 5091–5104
    OpenUrlAbstract
    1. Acampora D.,
    2. Avantaggiato V.,
    3. Tuorto F.,
    4. Simeone A.
    (1997) Genetic control of brain morphogenesis through Otx gene dosage requirement. Development 124, 3639–3650
    OpenUrlAbstract
    1. Acampora D.,
    2. Mazan S.,
    3. Lallemand Y.,
    4. Avantaggiato V.,
    5. Maury M.,
    6. Simeone A.,
    7. Brulet P.
    (1995) Forebrain and midbrain regions are deleted in Otx2/ mutants due to a defective anterior neuroectoderm specification during gastrulation. Development 121, 3279–3290
    OpenUrlAbstract
    1. Acampora D.,
    2. Mazan S.,
    3. Avvantaggiato V.,
    4. Barone P.,
    5. Tuorto F.,
    6. Lallemand Y.,
    7. Brulet P.,
    8. Simeone A.
    (1996) Epilepsy and brain abnormalities in mice lacking the Otx1 gene. Nature Genet 14, 218–222
    OpenUrlCrossRefPubMedWeb of Science
    1. Ang S. L.,
    2. Conlon R. A.,
    3. Jin O.,
    4. Rossant J.
    (1994) Positive and negative signals from mesoderm regulate the expression of mouse Otx2 in ectoderm explants. Development 120, 2979–2989
    OpenUrlAbstract
    1. Ang S. L.,
    2. Jin O.,
    3. Rhinn M.,
    4. Daigle N.,
    5. Stevenson L.,
    6. Rossant J.
    (1996) A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain. Development 122, 243–252
    OpenUrlAbstract
    1. Ang S. L.,
    2. Rossant J.
    (1993) Anterior mesendoderm induces mouse Engrailed genes in explant cultures. Development 118, 139–149
    OpenUrlAbstract
    1. Fekete D.
    (1996) Cell/ fate specification in the inner ear. Curr. Opin. Neurobiol 6, 533–541
    OpenUrlCrossRefPubMedWeb of Science
    1. Hirth F.,
    2. Therianos S.,
    3. Loop T.,
    4. Gehring W. J.,
    5. Reichert H.,
    6. Furukubo-Tokunaga K.
    (1995) Developmental defects in brainsegmentation caused by mutations of the homeobox gene orthodenticle and empty spiracles in Drosophila. Neuron 15, 15–20
    1. Kablar B.,
    2. Vignali R.,
    3. Menotti L.,
    4. Pannese M.,
    5. Andreazzoli M.,
    6. Polo C.,
    7. Giribaldi M. G.,
    8. Boncinelli E.,
    9. Barsacchi G.
    (1996) Xotx genes in the developing brain of Xenopus laevis. Mech. Dev 55, 145–158
    OpenUrlCrossRefPubMedWeb of Science
    1. Kiernan A. E.,
    2. Nunes F.,
    3. Wu D. K.,
    4. Fekete D. M.
    (1997) Unique expression domains of two members of a novel homeobox containing gene family suggest a role in semicircular canal formation during inner ear development. Dev. Biol 191, 216–229
    OpenUrl
    1. Leuzinger S.,
    2. Hirth F.,
    3. Gerlich D.,
    4. Acampora D.,
    5. Simeone A.,
    6. Gehring W.,
    7. Finkelstein R.,
    8. Furukubo-Tokunaga K.,
    9. Reichert H.
    (1998) Equivalence of the fly orthodenticle gene and the human OTX genes in embryonic brain development of Drosophila. Development 125, 1703–1710
    OpenUrlAbstract
    1. Li Y.,
    2. Allende M. L.,
    3. Finkelstein R.,
    4. Weinberg E. S.
    (1994) Expression of two zebrafish orthodenticle-related genes in the embryonic brain. Mech. Dev 48, 229–244
    OpenUrlCrossRefPubMedWeb of Science
    1. Matsuo I.,
    2. Kuratani S.,
    3. Kimura C.,
    4. Takeda N.,
    5. Aizawa S.
    (1995) Mouse Otx2 functions in the formation and patterning of rostral head. Genes Dev 9, 2646–2658
    OpenUrlAbstract/FREE Full Text
    1. Morsli H.,
    2. Choo D.,
    3. Ryan A.,
    4. Johnson R.,
    5. Wu D. K.
    (1998) Development of the mouse inner ear and origin of its sensory organs. J. Neurosci 18, 3327–3335
    OpenUrlAbstract/FREE Full Text
    1. Rhinn M.,
    2. Dierich A.,
    3. Shawlot W.,
    4. Behringer R.,
    5. Le Meur M.,
    6. Ang S.
    (1998) Sequential roles for Otx2 in visceral endoderm and neuroectoderm for forebrain and midbrain induction and specification. Development 125, 845–856
    OpenUrlAbstract
    1. Riddle R. D.,
    2. Johnson R. L.,
    3. Laufer E.,
    4. Tabin C.
    (1993) Sonic hedgehog mediates the polarizing activity of the ZPA. Cell 75, 1401–1416
    OpenUrlCrossRefPubMedWeb of Science
    1. Royet J.,
    2. Finkelstein R.
    (1995) Pattern formation in Drosophila head development: the role of the orthodenticle homeobox gene. Development 121, 3561–3572
    OpenUrlAbstract
    1. Royet J.,
    2. Finkelstein R.
    (1996) Hedgehog, wingless and orthodenticle specify adult head development in Drosophila. Development 122, 1849–1858
    OpenUrlAbstract
    1. Simeone A.,
    2. Acampora D.,
    3. Gulisano M.,
    4. Stornaiuolo A.,
    5. Boncinelli E.
    (1992) Nested expression domains of four homeobox genes in developing rostral brain. Nature 358, 687–690
    OpenUrlCrossRefPubMed
    1. Simeone A.,
    2. Acampora D.,
    3. Mallamaci A.,
    4. Stornaiuolo A.,
    5. Rosaria D'Apice M.,
    6. Nigro V.,
    7. Boncinelli E.
    (1993) A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectodem in the gastrulating mouse embryo. EMBO J 12, 2735–2747
    OpenUrlPubMedWeb of Science
    1. Steel K. P.,
    2. Davidson D. R.,
    3. Jackson I. J.
    (1992) TRP-2/DT, a new melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor. Development 115, 1111–1119
    OpenUrlAbstract
    1. Wu D. K.,
    2. Nunes F. D.,
    3. Choo D.
    (1998) Axial specification for sensory organs versus non-sensory structures of the chicken inner ear. Development 125, 11–20
    OpenUrlAbstract
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JOURNAL ARTICLES
Otx1 and Otx2 activities are required for the normal development of the mouse inner ear
H. Morsli, F. Tuorto, D. Choo, M.P. Postiglione, A. Simeone, D.K. Wu
Development 1999 126: 2335-2343;
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JOURNAL ARTICLES
Otx1 and Otx2 activities are required for the normal development of the mouse inner ear
H. Morsli, F. Tuorto, D. Choo, M.P. Postiglione, A. Simeone, D.K. Wu
Development 1999 126: 2335-2343;

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