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JOURNAL ARTICLES
The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo
P.H. Crossley, G.R. Martin
Development 1995 121: 439-451;
P.H. Crossley
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G.R. Martin
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Summary

Evidence is accumulating that members of the FGF gene family provide signals that act locally to regulate growth and patterning in vertebrate embryos. In this report, we provide a detailed analysis of the mouse Fgf8 gene. We have mapped the Fgf8 locus to the distal region of mouse chromosome 19, and sequenced the 5′ coding region of the gene. Our data identify a new coding exon, and locate multiple splice donor and splice acceptor sites that can be used to produce at least seven transcripts encoding a family of secreted FGF8 proteins with different N termini. From these results, it appears that Fgf8 is structurally the most complex member of the FGF family described to date. In the embryo, many of the regions in which Fgf8 RNA is localized are known to direct outgrowth and patterning, including the apical ectodermal ridge of the limb bud, the primitive streak and tail bud, the surface ectoderm overlying the facial primorida and the midbrain-hindbrain junction, suggesting that FGF8 may be a component of the regulatory signals that emanate from these regions.

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 signaling in the early specification of mesoderm in Xenopus. Development 118, 477–487
    OpenUrlAbstract
    1. Baird A.
    (1994) Fibroblast growth factors: activities and significance of non-neurotrophin neurotrophic growth factors. Curr. Opin. Neurobiol 4, 78–86
    OpenUrlCrossRefPubMed
    1. Bally-Cuif L.,
    2. Alvarado-Mallart R.-M.,
    3. Darnell D.,
    4. Wassef M.
    (1992) Relationship between Wnt-1 and En-2 expression domains during early development of normal and ectopic met-mesencephalon. Development 115, 999–1009
    OpenUrlAbstract
    1. Basilico C.,
    2. Moscatelli D.
    (1992) The FGF family of growth factors and oncogenes. Adv. Cancer Res 59, 115–165
    OpenUrlPubMedWeb of Science
    1. Bastian H.,
    2. Gruss P.
    (1990) A murine even-skipped homologue, Evx 1, is expressed during early embryogenesis and neurogenesis in a biphasic manner. EMBO J 9, 1839–1852
    OpenUrlPubMedWeb of Science
    1. Bellosta P.,
    2. Talarico D.,
    3. Rogers D.,
    4. Basilico C.
    (1993) Cleavage of K-FGF produces a truncated molecule with increased biological activity and receptor binding affinity. J. Cell Biol 121, 705–713
    OpenUrlAbstract/FREE Full Text
    1. Blum M.,
    2. Gaunt S. J.,
    3. Cho K. W. Y.,
    4. Steinbeissser H.,
    5. Blumberg B.,
    6. Bittner D.,
    7. De Robertis E. M.
    (1992) Gastrulation in the mouse: the role of the homeobox gene goosecoid. Cell 69, 1097–1106
    OpenUrlCrossRefPubMedWeb of Science
    1. Blumberg B.,
    2. Wright C.,
    3. De Robertis E.,
    4. Cho K.
    (1991) Organizer-specific homeobox genes in Xenopus laevis embryos. Science 253, 194–196
    OpenUrlAbstract/FREE Full Text
    1. Church G. M.,
    2. Gilbert W.
    (1984) Genomic sequencing. Proc. Natl. Acad. Sci. USA 81, 1991–1995
    OpenUrlAbstract/FREE Full Text
    1. Davies P.,
    2. Poirier C.,
    3. Deltour L.,
    4. Montagutelli X.
    (1994) Genetic reassignment of the insulin-1 (ins1) gene to distal mouse chromosome 19. Genomics 21, 665–667
    OpenUrlCrossRefPubMed
    1. de Lapeyriere O.,
    2. Ollendorff V.,
    3. Planche J.,
    4. Ott M. O.,
    5. Pizette S.,
    6. Coulier F.,
    7. Birnbaum D.
    (1993) Expression of the Fgf6 gene is restricted to developing skeletal muscle in the mouse embryo. Development 118, 601–611
    OpenUrlAbstract
    1. DeRuiter M.,
    2. Poelmann R.,
    3. VanderPlas-de Vries I.,
    4. Mentink M.,
    5. Gittenberger-de Groot A.
    (1992) The development of the myocardium and endocardium in mouse embryos. Fusion of two heart tubes?. Anat. Embryol 185, 461–473
    OpenUrlPubMed
    1. Dickinson M.,
    2. McMahon A.
    (1992) The role of Wnt genes in vertebrate development. Curr. Opin. Genet. Dev 2, 562–566
    OpenUrlCrossRefPubMed
    1. Dono R.,
    2. Zeller R.
    (1994) Cell-type-specific nuclear translocation of Fibroblast Growth Factor-2 isoforms during chicken kidney and limb morphogenesis. Dev. Biol 163, 316–330
    OpenUrlCrossRefPubMedWeb of Science
    1. Dush M. K.,
    2. Martin G. R.
    (1992) Analysis of mouse Evx genes; Evx-1 displays graded expression in the primitive streak. Dev. Biol 151, 273–287
    OpenUrlCrossRefPubMedWeb of Science
    1. Echelard Y.,
    2. Epstein D.,
    3. St-Jacques B.,
    4. Shen L.,
    5. Mohler J.,
    6. McMahon J.,
    7. McMahon A.
    (1993) Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity. Cell 75, 1417–1430
    OpenUrlCrossRefPubMedWeb of Science
    1. Fallon J. F.,
    2. Lopez A.,
    3. Ros M. A.,
    4. Savage M. P.,
    5. Olwin B. B.,
    6. Simandl B. K.
    (1994) FGF-2: Apical ectodermal ridge growth signal for chick limb development. Science 264, 104–107
    OpenUrlAbstract/FREE Full Text
    1. Frohman M. A.,
    2. Boyle M.,
    3. Martin G. R.
    (1990). Isolation of the mouse Hox-2.9 gene; analysis of embryonic expression suggests that positional information along the anterior-posterior axis is specified by mesoderm. Development 110, 589–607
    OpenUrlAbstract/FREE Full Text
    1. Fu Y.,
    2. Spirito P.,
    3. Yu Z.,
    4. Biro S.,
    5. Sasse J.,
    6. Lei J.,
    7. Ferrans V.,
    8. Epstein S.,
    9. Casscells W.
    (1991) Acidic fibroblast growth factor in the developing rat embryo. J. Cell Biol 114, 1261–1273
    OpenUrlAbstract/FREE Full Text
    1. Gonzalez A.,
    2. Buscglia M.,
    3. Ong M.,
    4. Baird A.
    (1990) Distribution of basic Fibroblast Growth Factor in the 18-day rat fetus: localization in the basement membranes of diverse tissues. J. Cell Biol 110, 753–765
    OpenUrlAbstract/FREE Full Text
    1. Han J.-K.,
    2. Martin G. R.
    (1993) Embryonic expression of Fgf-6 is restricted to the skeletal muscle lineage. Dev. Biol 158, 549–554
    OpenUrlCrossRefPubMedWeb of Science
    1. Haub O.,
    2. Goldfarb M.
    (1991) Expression of the fibroblast growh factor-5 gene in the mouse embryo. Development 112, 397–406
    OpenUrlAbstract
    1. Hebert J. M.,
    2. Boyle M.,
    3. Martin G. R.
    (1991) mRNA localization studies suggest that murine Fibroblast Growth Factor-5 plays a role in gastrulation. Development 112, 407–415
    OpenUrlAbstract
    1. Hogan B.,
    2. Thaller C.,
    3. Eichele G.
    (1992) Evidence that Hensen's node is a site of retinoic acid synthesis. Nature 359, 237–241
    OpenUrlCrossRefPubMed
    1. Hornbruch A.,
    2. Wolpert L.
    (1986) Positional signalling by Hensen's node when grafted to the chick limb bud. J. Embryol. Exp. Morph 94, 257–265
    OpenUrlPubMed
    1. Johnson D. E.,
    2. Williams L. T.
    (1993) Structural and functional diversity in the FGF receptor multigene family. Adv. Cancer Res 60, 1–41
    OpenUrlPubMedWeb of Science
    1. Kaufman M.,
    2. Navaratnam B.
    (1981) Early differentiation of the heart in mouse embryos. J. Anat 133, 235–246
    OpenUrlPubMedWeb of Science
    1. Kimelman D.,
    2. Christian J.,
    3. Moon R.
    (1992) Synergistic principles of development: overlapping patterning systems in Xenopus mesoderm induction. Development 116, 1–9
    OpenUrlAbstract
    1. Kingsley D.
    (1994) The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms. Genes Dev 8, 133–146
    OpenUrlFREE Full Text
    1. Kouhara H.,
    2. Koga M.,
    3. Kasayama S.,
    4. Tanaka A.,
    5. Kishimoto T.,
    6. Sato B.
    (1994) Transforming activity of a newly cloned androgen-induced growth factor. Oncogene 9, 455–462
    OpenUrlPubMed
    1. Lawson K. A.,
    2. Meneses J. J.,
    3. Pedersen R. A.
    (1991) Clonal analysis of epiblast fate during germ layer formation in the mouse embryo. Development 113, 891–911
    OpenUrlAbstract
    1. Lumsden A.
    (1988) Spatial organisation of the epithelium and the role of neural crest cells in the initiation of the mammalian tooth germ. Development 103, 155–169
    1. Mansour S. L.,
    2. Goddard J. M.,
    3. 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
    OpenUrlAbstract/FREE Full Text
    1. Marin F.,
    2. Puelles L.
    (1994) Patterning of the embryonic avian midbrain after experimental inversions: a polarizing activity from the isthmus. Dev. Biol 163, 19–37
    OpenUrlCrossRefPubMedWeb of Science
    1. Mason I.,
    2. Fuller-Pace F.,
    3. Smith R.,
    4. Dickson C.
    (1994) FGF-7 (keratinocyte growth factor) expression during mouse development suggests roles in myogenesis, forebrain regionalization and epithelial-mesenchymal interactions. Mech. Dev 45, 15–30
    OpenUrlCrossRefPubMedWeb of Science
    1. Melton D.,
    2. Jessell T.
    (1993) Diffusible factors in vertebrate embryonic induction. Cell 68, 257–270
    OpenUrl
    1. Moon R.,
    2. Christian J.
    (1992) Competence modifiers synergize with growth factors during mesoderm induction and patterning in Xenopus. Cell 71, 709–712
    OpenUrlCrossRefPubMedWeb of Science
    1. Niswander L.,
    2. Martin G. R.
    (1992) Fgf-4 expression during gastrulation, myogenesis, limb and tooth development in the mouse. Development 114, 755–768
    OpenUrlAbstract
    1. Niswander L.,
    2. Martin G. R.
    (1993) FGF-4 regulates expression of Evx-1 in the developing mouse limb. Development 119, 287–294
    OpenUrlAbstract
    1. Niswander L.,
    2. Tickle C.,
    3. Vogel A.,
    4. Booth I.,
    5. Martin G. R.
    (1993) FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb. Cell 75, 579–587
    OpenUrlCrossRefPubMedWeb of Science
    1. Niswander L. A.,
    2. Jeffrey S.,
    3. Martin G. R.,
    4. Tickle C.
    (1994) A positive feedback loop coordinates growth and patterning in the vertebrate limb. Nature 371, 609–612
    OpenUrlCrossRefPubMed
    1. Nusse R.,
    2. Varmus H.
    (1992) Wnt genes. Cell 69, 1073–1087
    OpenUrlCrossRefPubMedWeb of Science
    1. Orr-Urtreger A.,
    2. Givol D.,
    3. Yayon A.,
    4. Yarden Y.,
    5. Lonai P.
    (1991) Developmental expression of two murine fibroblast growth factor receptors, flg and bek. Development 113, 1419–1434
    OpenUrlAbstract
    1. Orr-Urtreger A.,
    2. Bedford M. T.,
    3. Burakova T.,
    4. Arman E.,
    5. Zimmer Y.,
    6. Yayon A.,
    7. Givol D.,
    8. Lonai P.
    (1993) Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2). Dev Biol 158, 475–86
    OpenUrlCrossRefPubMedWeb of Science
    1. Parr B.,
    2. Shea M.,
    3. Vassileva G.,
    4. McMahon A.
    (1993) Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds. Development 119, 247–261
    OpenUrlAbstract
    1. Peters K. G.,
    2. Werner S.,
    3. Williams L. T.
    (1992) Two FGF receptor genes are differentially expressed in epithelial and mesenchymal tissues during limb formation and organogenesis in the mouse. Development 114, 233–243
    OpenUrlAbstract
    1. Peters K.,
    2. Ornitz D.,
    3. Werner S.,
    4. Williams L.
    (1993) Unique expression pattern of the FGF receptor 3 gene during mouse organogenesis. Dev. Biol 155, 423–430
    OpenUrlCrossRefPubMedWeb of Science
    1. Richman J. M.,
    2. Tickle C.
    (1989) Epithelia are interchangeable between facial primordia of chick embryos and morphogenesis is controlled by the mesenchyme. Dev. Biol 136, 201–210
    OpenUrlCrossRefPubMed
    1. Richman J. M.,
    2. Tickle C.
    (1992) Epithelial-mesenchymal interactions in the outgrowth of limb buds and facial primordia in chick embryos. Dev. Biol 154, 299–308
    OpenUrlCrossRefPubMedWeb of Science
    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. Rijli M. F.,
    2. Mark M.,
    3. Lakkaraju S.,
    4. Dierich A.,
    5. Dolle P.,
    6. Chambon P.
    (1993) A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene. Cell 75, 1333–1349
    OpenUrlCrossRefPubMedWeb of Science
    1. Rowe L.,
    2. Nadeau J.,
    3. Turner R.,
    4. Frankel W.,
    5. Letts V.,
    6. Eppig J.,
    7. Ko M.,
    8. Thurston S.,
    9. Birkenmeir E.
    (1994) Maps from two interspecificbackcross DNA panels available as a community genetic mapping resource. Mammal. Genome 5, 253–274
    OpenUrlCrossRefPubMedWeb of Science
    1. Rubenstein J.,
    2. Martinez S.,
    3. Puelles L.
    (1994) The prosomeric model: a proposal for the organization of the embryonic vertebrate forebrain. Science 266, 578–580
    OpenUrlFREE Full Text
    1. Ruiz i Altaba A.,
    2. Choi T.,
    3. Melton D. A.
    (1991) Expression of the Xhox3 homeobox protein in Xenopus embryos: blocking its early function suggests the requirement of Xhox3 for normal posterior development. Dev. Growth and Diff 33, 651–669
    OpenUrlCrossRef
    1. Ruiz i Altaba A.,
    2. Melton D. A.
    (1989) Interaction between peptide growth factors and homoeobox genes in the establishment of antero-posterior polarity in frog embryos. Nature 341, 33–38
    OpenUrlCrossRefPubMed
    1. Sato B.,
    2. Kouhara H.,
    3. Koga M.,
    4. Kasayama S.,
    5. Saito H.,
    6. Sumitani S.,
    7. Hashimoto K.,
    8. Kishimoto T.,
    9. Tanaka A.,
    10. Matsumoto K.
    (1993) Androgen-induced growth factor and its receptor: demonstation of the androgen-induced autocrine loop in mouse mammary carcinoma cells. J. Steroid Biochem. Molec. Biol 47, 91–98
    OpenUrlCrossRefPubMed
    1. Savage M. P.,
    2. Hart C. E.,
    3. Riley B.,
    4. Sasse J.,
    5. Olwin B. B.,
    6. Fallon J. R.
    (1993) Distribution of FGF-2 suggests it has a role in chick limb bud growth. Dev. Dynamics 198, 159–170
    OpenUrlPubMedWeb of Science
    1. Shackleford G. M.,
    2. Willert K.,
    3. Wang J.,
    4. Varmus H.
    (1993) The Wnt1 proto-oncogene induces changes in morphology, gene expression, and growth factor responsiveness in PC12 cells. Neuron 11, 865–875
    OpenUrlCrossRefPubMed
    1. Stark K. L.,
    2. McMahon J. A.,
    3. McMahon A. P.
    (1991) FGFR-4, a new member of the fibroblast growth factor receptor family expressed in the definitive endoderm and skeletal muscle lineages of the mouse. Development 113, 641–651
    OpenUrlAbstract
    1. Tabin C. J.
    (1991) Retinoids, homeoboxes, and growth factors: toward molecular models for limb development. Cell 66, 199–217
    OpenUrlCrossRefPubMedWeb of Science
    1. Tanaka A.,
    2. Miyamoto K.,
    3. Minamino N.,
    4. Takeda M.,
    5. Sato B.,
    6. Matsuo H.,
    7. Matsumoto K.
    (1992) Cloning and characterization of an androgen-induced growth factor essential for the androgen-dependent growth of mouse mammary carcinoma cells. Proc. Natl. Acad. Sci. USA 89, 8928–8932
    OpenUrlAbstract/FREE Full Text
    1. Tickle C.,
    2. Eichele G.
    (1994) Vertebrate limb development. Annu. Rev. Cell Biol 10, 121–152
    OpenUrlCrossRefWeb of Science
    1. Wanek N.,
    2. Muneoka K.,
    3. Holler-Dinsmore G.,
    4. Burton R.,
    5. Bryant S. V.
    (1989) A staging system for mouse limb development. J. Exp. Zool 249, 41–49
    OpenUrlCrossRefPubMedWeb of Science
    1. Wedden S. E.
    (1987) Epithelial-mesenchymal interactions in the developing chick facial primordia and the target of retinoid action. Development 99, 341–351
    OpenUrlAbstract
    1. Wilkinson D. G.,
    2. Bailes J. A.,
    3. McMahon A. P.
    (1987) Expression of the proto-oncogene int-1 is restricted to specific neural cells in the developing mouse embryo. Cell 50, 79–88
    OpenUrlCrossRefPubMedWeb of Science
    1. Wilkinson D. G.,
    2. Bhatt S.,
    3. McMahon A. P.
    (1989) Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development. Development 105, 131–136
    OpenUrlAbstract
    1. Wilkinson D. G.,
    2. Peters G.,
    3. Dickson C.,
    4. 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
    OpenUrlPubMedWeb of Science
    1. Yamaguchi T. P.,
    2. Conlon R. A.,
    3. Rossant J.
    (1992) Expression of the fibroblast growth factor receptor FGFR-1/flg during gastrulation and segmentation in the mouse embryo. Dev. Biol 152, 75–88
    OpenUrlCrossRefPubMedWeb of Science
    1. Yu Y.,
    2. Kah H.,
    3. Golden J.,
    4. Migchielsen A.,
    5. Goetzl E.,
    6. Turck C.
    (1992) An acidic Fibroblast Growth Factor protein generated by alternative splicing acts like and antagonist. J. Exp. Med 175, 1073–1080
    OpenUrlAbstract/FREE Full Text
    1. Zúñiga-Mejía-Borja A.,
    2. Meijers C.,
    3. Zeller R.
    (1993) Expression of alternatively spliced bFGF first coding exons and antisense mRNAs during chicken embryogenesis. Dev. Biol 157, 110–118
    OpenUrlCrossRefPubMedWeb of Science
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JOURNAL ARTICLES
The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo
P.H. Crossley, G.R. Martin
Development 1995 121: 439-451;
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JOURNAL ARTICLES
The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo
P.H. Crossley, G.R. Martin
Development 1995 121: 439-451;

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