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JOURNAL ARTICLES
Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation
K.L. Kroll, E. Amaya
Development 1996 122: 3173-3183;
K.L. Kroll
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E. Amaya
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Summary

We have developed a simple approach for large-scale transgenesis in Xenopus laevis embryos and have used this method to identify in vivo requirements for FGF signaling during gastrulation. Plasmids are introduced into decondensed sperm nuclei in vitro using restriction enzyme-mediated integration (REMI). Transplantation of these nuclei into unfertilized eggs yields hundreds of normal, diploid embryos per day which develop to advanced stages and express integrated plasmids nonmosaically. Transgenic expression of a dominant negative mutant of the FGF receptor (XFD) after the mid-blastula stage uncouples mesoderm induction, which is normal, from maintenance of mesodermal markers, which is lost during gastrulation. By contrast, embryos expressing XFD contain well-patterned nervous systems despite a putative role for FGF in neural induction.

Reference

    1. Amaya E.,
    2. Musci T. J.,
    3. Kirschner M. W.
    (1991) Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos. Cell 66, 257–270
    OpenUrlCrossRefPubMedWeb of Science
    1. Amaya E.,
    2. Stein P. A.,
    3. Musci T. J.,
    4. Kirschner M. W.
    (1993) FGF signalling in the early specification of mesoderm in Xenopus. Development 118, 477–487
    OpenUrlAbstract
    1. Barbacid M.
    (1995) Neurotrophic factors and their receptors. Current Opinion in Cell Biology 7, 148–155
    OpenUrlCrossRefPubMedWeb of Science
    1. Bieker J. J.,
    2. Yazdani-Buicky M.
    (1992) Distribution of type II collagen mRNA in Xenopus embryos visualized by whole-mount in situ hybridization. J. Histochem. Cytochem 40, 1117–1120
    OpenUrlAbstract/FREE Full Text
    1. Bolce M. E.,
    2. Hemmati-Brivanlou A.,
    3. Kushner P. D.,
    4. Harland R. M.
    (1992) Ventral ectoderm of Xenopus forms neural tissue, including hindbrain, in response to activin. Development 115, 681–688
    OpenUrlAbstract
    1. Brakenhoff R. H.,
    2. Ruuls R. C.,
    3. Jacobs E. H.,
    4. Schoenmakers J. G.,
    5. Lubsen N. H.
    (1991) Transgenic Xenopus laevis tadpoles: a transient in vivo model system for the manipulation of lens function and lens development. Nucl. Acids Res 19, 1279–1284
    OpenUrlAbstract/FREE Full Text
    1. Chalfie M.,
    2. Tu Y.,
    3. Euskirchen G.,
    4. Ward W. W.,
    5. Prasher D. C.
    (1994) Green fluorescent protein as a marker for gene expression. Science 263, 802–805
    OpenUrlAbstract/FREE Full Text
    1. Chesley P.
    (1935) Development of the short-tailed mutation in the house mouse. J. Exp. Zool 70, 429–459
    OpenUrlCrossRefWeb of Science
    1. Clarke J. D. W.,
    2. Holder N.,
    3. Soffe S. R.,
    4. Storm-Mathisen J.
    (1991) Neuroanatomical and functional analysis of neural tube formation in notochordless Xenopus embryos; laterality of the ventral spinal cord is lost. Development 112, 499–516
    OpenUrlAbstract
    1. Condie B. G.,
    2. Brivanlou A. H.,
    3. Harland R. M.
    (1990) Most of the homeobox-containing Xhox 36 transcripts in early Xenopus embryos cannot encode a homeodomain protein. Mol. Cell. Biol 10, 3376–3385
    OpenUrlAbstract/FREE Full Text
    1. Cornell R. A.,
    2. Kimelman D.
    (1994) Activin-mediated mesoderm induction requires FGF. Development 120, 453–462
    OpenUrlAbstract
    1. Cox W. G.,
    2. Hemmati-Brivanlou A.
    (1995) Caudalization of neural fate by tissue recombination and bFGF. Development 121, 4349–4358
    OpenUrlAbstract
    1. Cross G. S.,
    2. Wilson C.,
    3. Erba H. P.,
    4. Woodland H. R.
    (1988) Cytoskeletal actin gene families of Xenopus borealis and Xenopus laevis. J. Molec. Evol 27, 17–28
    OpenUrlCrossRefPubMed
    1. Cunliffe V.,
    2. Smith J. C.
    (1992) Ectopic mesoderm formation in Xenopus embryos caused by widespread expression of a Brachyury homologue. Nature 358, 427–30
    OpenUrlCrossRefPubMed
    1. Doniach T.
    (1995) bFGF as an inducer of anteroposterior neural pattern. Cell 83, 1067–1070
    OpenUrlCrossRefPubMedWeb of Science
    1. Doniach T.,
    2. Musci T. J.
    (1995) Induction of anteroposterior neural pattern in Xenopus: evidence for a quantitative mechanism. Mech. Dev 53, 403–413
    OpenUrlCrossRefPubMedWeb of Science
    1. Doniach T.,
    2. Phillips C. R.,
    3. Gerhart J. C.
    (1992) Planar induction of anteroposterior pattern in the developing central nervous system of Xenopus laevis. Science 257, 542–545
    OpenUrlAbstract/FREE Full Text
    1. Frank D.,
    2. Harland R. M.
    (1992) Localized expression of a Xenopus POU gene depends on cell-autonomous transcriptional activation and induction-dependent inactivation. Development 115, 439–448
    OpenUrlAbstract
    1. Griffin K.,
    2. Patient R.,
    3. Holder N.
    (1995) Analysis of FGF function in normal and no tail zebrafish embryos reveals separate mechanisms for formation of the trunk and the tail. Development 121, 2983–2994
    OpenUrlAbstract
    1. Halpern M. E.,
    2. Ho R. K.,
    3. Walker C.,
    4. Kimmel C. B.
    (1993) Induction of muscle pioneers and floor plate is distinguished by the zebrafish no tail mutation. Cell 75, 99–111
    OpenUrlCrossRefPubMedWeb of Science
    1. Harland R. M.
    (1991) In situ hybridization: an improved whole-mount method for Xenopus embryos. Meth. in Cell Biol 36, 685–695
    OpenUrlCrossRefPubMedWeb of Science
    1. Harland R. M.
    (1994) The transforming growth factor beta family and induction of the vertebrate mesoderm: Bone morphogenetic proteins are ventral inducers. Proc. Natl. Acad. Sci. USA 91, 10243–10246
    OpenUrlFREE Full Text
    1. Harland R. M.,
    2. Misher L.
    (1988) Stability of RNA in developing Xenopus embryos and identification of a destabilizing sequence in TFIIIA RNA. Development 102, 837–852
    OpenUrlAbstract/FREE Full Text
    1. Heasman J.,
    2. Holwill S.,
    3. Wylie C. C.
    (1991) Fertilization of cultured Xenopus oocytes and use in studies of maternally inherited molecules. Meth. in Cell Biol 36, 213–30
    OpenUrlPubMed
    1. Heim R.,
    2. Cubitt A. B.,
    3. Tsien R. Y.
    (1995) Improved green fluorescence. Nature 373, 663–664
    OpenUrlCrossRefPubMed
    1. Isaacs H. V.,
    2. Pownall M. E.,
    3. Slack J. M. W.
    (1994) eFGF regulates Xbra expression during Xenopus gastrulation. EMBO J 13, 4469–4481
    OpenUrlPubMedWeb of Science
    1. Isaacs H. V.,
    2. Tannahill D.,
    3. Slack J. M. W.
    (1992) Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification. Development 114, 711–720
    OpenUrlAbstract
    1. Itoh N.,
    2. Mima T.,
    3. Mikawa T.
    (1996) Loss of fibroblast growth factor receptors is necessary for terminal differentiation of embryonic limb muscle. Development 122, 291–300
    OpenUrlAbstract
    1. Kengaku M.,
    2. Okamoto H.
    (1993) Basic fibroblast growth factor induces differentiation of neural tube and neural crest lineages of cultured ectoderm cells from Xenopus gastrula. Development 119, 1067–1078
    OpenUrlAbstract
    1. Kengaku M.,
    2. Okamoto H.
    (1995) bFGF as a possible morphogen for the anteroposterior axis fo the centrol nervous system in Xenopus. Development 121, 3121–3130
    OpenUrlAbstract
    1. Kimelman D.,
    2. Christian J. L.,
    3. Moon R. T.
    (1992) Synergistic principles of development: overlapping patterning systems in Xenopus mesoderm induction. Development 116, 1–9
    OpenUrlAbstract
    1. Kimelman D.,
    2. Kirschner M.
    (1987) Synergistic induction of mesoderm by FGF and TGF-beta and the identification of an mRNA coding for FGF in the early Xenopus embryo. Cell 51, 869–877
    OpenUrlCrossRefPubMedWeb of Science
    1. Kinoshita N.,
    2. Minshull J.,
    3. Kirschner M. W.
    (1995) The identification of two novel ligands of the FGF receptor by a yeast screening method and their activity in Xenopus development. Cell 83, 621–630
    OpenUrlCrossRefPubMedWeb of Science
    1. Kintner C. R.,
    2. Brockes J. P.
    (1984) Monoclonal antibodies identify blastemal cells derived from dedifferentiating muscle in newt limb regeneration. Nature 308, 67–69
    OpenUrlCrossRefPubMed
    1. Kroll K. L.,
    2. Gerhart J. C.
    (1994) Transgenic X. laevis embryos from eggs transplanted with nuclei of transfected cultured cells. Science 266, 650–653
    OpenUrlAbstract/FREE Full Text
    1. LaBonne C.,
    2. Whitman M.
    (1994) Mesoderm induction by activin requires FGF-mediated intracellular signals. Development 120, 463–472
    OpenUrlAbstract
    1. Lamb T. M.,
    2. Harland R. M.
    (1995) Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior pattern. Development 121, 3627–3636
    OpenUrlAbstract
    1. Lamb T. M.,
    2. Knetcht A. K.,
    3. Smith W. C.,
    4. Stachel S. E.,
    5. Economides A. N.,
    6. Stahl N.,
    7. Yancopolous G. D.,
    8. Harland R. M.
    (1993) Neural induction by the secreted polypeptide noggin. Science 262, 713–718
    OpenUrlAbstract/FREE Full Text
    1. Launay C.,
    2. Fromentoux V.,
    3. Shi D.-L.,
    4. Boucaut J.-C.
    (1996) A truncated FGF receptor blocks neural induction by endogenous Xenopus inducers. Development 122, 869–880
    OpenUrlAbstract
    1. Lemaire P.,
    2. Gurdon J. B.
    (1994) A role for cytoplasmic determinants in mesoderm patterning: cell-autonomous activation of the goosecoid and Xwnt-8 genes along the dorsoventral axis of early Xenopus embryos. Development 120, 1191–1199
    OpenUrlAbstract
    1. Mohun T. J.,
    2. Garrett N.,
    3. Gurdon J. B.
    (1986) Upstream sequences required for tissue-specific activation of the cardiac actin gene in Xenopus laevis embryos. EMBO J 5, 3185–3193
    OpenUrlPubMedWeb of Science
    1. Morasso M. I.,
    2. Mahon K. A.,
    3. Sargent T. D.
    (1995) A Xenopus distal-less gene in transgenic mice: conserved regulation in distal limb epidermis and other sites of epithelial-mesenchymal interaction. Proc. Natl. Acad. Sci. USA 92, 3968–3972
    OpenUrlAbstract/FREE Full Text
    1. Murray A. W.
    (1991) Cell cycle extracts. Meth. in Cell Biol 36, 581–605
    OpenUrlCrossRefPubMed
    1. Musci T. J.,
    2. Amaya E.,
    3. Kirschner M. W.
    (1990) Regulation of the fibroblast growth factor receptor in early Xenopus embryos. Proc. Natl. Acad. Sci. USA 87, 8365–8369
    OpenUrlAbstract/FREE Full Text
    1. Oschwald R.,
    2. Richter K.,
    3. Grunz H.
    (1991) Localization of a nervous system-specific class II beta-tubulin gene in Xenopus laevis embryos by whole-mount in situ hybridization. Int. J. Dev. Biol 35, 399–405
    OpenUrlPubMed
    1. Papalopulu N.,
    2. Clarke J. W. D.,
    3. Bradley L.,
    4. Wilkinson D.,
    5. Krumlauf R.,
    6. Holder N.
    (1991) Retinoic acid causes abnormal development and segmental patterning of the anterior hindbrain in Xenopus embryos. Development 113, 1145–1158
    OpenUrlAbstract
    1. Papalopulu N.,
    2. Kintner C.
    (1993) Xenopus Distal-less related homeobox genes are expressed in the developing forebrain and are induced by planar signals. Development 117, 961–975
    OpenUrlAbstract
    1. Schiestl R. H.,
    2. Petes T. D.
    (1991) Integration of DNA fragments by illegitimate recombination in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA 88, 7585–7589
    OpenUrlAbstract/FREE Full Text
    1. Schulte-Merker S.,
    2. Smith J. C.
    (1995) Mesoderm formation in response to Brachyury requires FGF signalling. Curr. Biol 5, 62–67
    OpenUrlCrossRefPubMedWeb of Science
    1. Shih J.,
    2. Keller R.
    (1992) The epithelium of the dorsal marginal zone of Xenopus has organizer properties. Development 116, 887–899
    OpenUrlAbstract/FREE Full Text
    1. Slack J. M. W.
    (1994) Inducing factors in Xenopus early embryos. Curr. Biol 4, 116–126
    OpenUrlCrossRefPubMedWeb of Science
    1. Slack J. M. W.,
    2. Darlington B. G.,
    3. Heath J. K.,
    4. Godsave S. F.
    (1987) Mesoderm induction in early Xenopus embryos by heparin-binding growth factors. Nature 326, 197–200
    OpenUrlCrossRefPubMed
    1. Slack J. M. W.,
    2. Tannahill D.
    (1992) Mechanism of anteroposterior axis specification in vetrebrates: Lessons from the amphibians. Development 114, 285–302
    OpenUrlAbstract
    1. Smith J. C.,
    2. Price B. M. J.,
    3. Green J. B. A.,
    4. Weigel D.,
    5. Herrmann B. G.
    (1991) Expression of a Xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm induction. Cell 67, 79–87
    OpenUrlCrossRefPubMedWeb of Science
    1. Smith W. C.,
    2. Harland R. M.
    (1992) Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos. Cell 70, 829–840
    OpenUrlCrossRefPubMedWeb of Science
    1. Tannahill D.,
    2. Isaacs H. V.,
    3. Close M. J.,
    4. Peters G.,
    5. Slack J. M. W.
    (1992) Developmental expression of the Xenopusint-2 (FGF-3) gene: activation by mesodermal and neural induction. Development 115, 695–702
    OpenUrlAbstract/FREE Full Text
    1. Turner D. L.,
    2. Weintraub H.
    (1994) Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate. Genes Dev 8, 1434–1447
    OpenUrlAbstract/FREE Full Text
    1. Vize P. D.,
    2. Melton D. A.,
    3. Hemmati-Brivanlou A.,
    4. Harland R. M.
    (1991) Assays for gene function in developing Xenopus embryos. Meth. Cell Bio 36, 367–387
    OpenUrlPubMed
    1. Vodicka M. A.,
    2. Gerhart J. C.
    (1995) Blastomere derivation and domains of gene expression in the Spemann Organizer of Xenopus laevis. Development 121, 3505–3518
    OpenUrlAbstract
    1. von Dassow G.,
    2. Schmidt J.,
    3. Kimelman D.
    (1993) Induction of the Xenopus organizer: Expression and regulation of Xnot, a novel FGF and activin-inducible homeobox gene. Genes Dev 7, 355–366
    OpenUrlAbstract/FREE Full Text
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JOURNAL ARTICLES
Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation
K.L. Kroll, E. Amaya
Development 1996 122: 3173-3183;
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JOURNAL ARTICLES
Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation
K.L. Kroll, E. Amaya
Development 1996 122: 3173-3183;

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