Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Advertising
    • Feedback
    • Institutional usage stats (logged-in users only)
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

User menu

  • Log in
  • Log out

Search

  • Advanced search
Development
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

supporting biologistsinspiring biology

Development

  • Log in
Advanced search

RSS  Twitter  Facebook  YouTube 

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Advertising
    • Feedback
    • Institutional usage stats (logged-in users only)
JOURNAL ARTICLES
Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain
H. Shamim, R. Mahmood, C. Logan, P. Doherty, A. Lumsden, I. Mason
Development 1999 126: 945-959;
H. Shamim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
R. Mahmood
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
C. Logan
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
P. Doherty
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
A. Lumsden
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
I. Mason
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

Experiments involving tissue recombinations have implicated both early vertical and later planar signals in the specification and polarisation of the midbrain. Here we investigate the role of fibroblast growth factors in regulating these processes in the avian embryo. We show that Fgf4 is expressed in the notochord anterior to Hensen's node before transcripts for the earliest molecular marker of midbrain tissue in the avian embryo, En1, are detected. The presence of notochord is required for the expression of En1 in neural plate explants in vitro and FGF4 mimics this effect of notochord tissue. Subsequently, a second member of the fibroblast growth factor family, Fgf8, is expressed in the isthmus in a manner consistent with it providing a polarising signal for the developing midbrain. Using a retroviral vector to express En1 ectopically, we show that En1 can induce Fgf8 expression in midbrain and posterior diencephalon. Results of the introduction of FGF8 protein into the anterior midbrain or posterior diencephalon are consistent with it being at least part of the isthmic activity which can repolarise the former tissue and respecify the latter to a midbrain fate. However, the ability of FGF8 to induce expression of genes which have earlier onsets of expression than Fgf8 itself, namely En1 and Pax2, strongly suggests that the normal function of FGF8 is in maintaining patterns of gene expression in posterior midbrain. Finally, we provide evidence that FGF8 also provides mitogenic stimulation during avian midbrain development.

Reference

    1. Abud H. E.,
    2. Skinner J. A.,
    3. McDonald F. J.,
    4. Bedford M. T.,
    5. Lonai P.,
    6. Heath J. K.
    (1996) Ectopic expression of Fgf-4 in chimeric mouse embryos induces the expression of early markers of limb development in the lateral ridge. Dev. Genet 19, 51–65
    OpenUrlCrossRefPubMedWeb of Science
    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. Alvarado-Mallart R.-M.,
    2. Martinez S.,
    3. Lance-Jones C.
    (1990) Pluripotentiality of the 2-day-old avian germinative neuroepithelium. Dev. Biol 139, 75–88
    OpenUrlCrossRefPubMedWeb of Science
    1. Alvarado-Mallart R.-M.,
    2. Sotelo C.
    (1984) Homotopic and heterotopic transplantations of quail tectal primordia in chick embryos: organisation of the retinotectal projections in the chimeric embryos. Dev. Biol 103, 378–398
    OpenUrlCrossRefPubMed
    1. Alvarado-Mallart R. M.
    (1993) Fate and potentialities of the avian mesencephalic/metencephalic neuroepithelium. J. Neurobiol 24, 1341–1355
    OpenUrlCrossRefPubMedWeb of Science
    1. Alvarez I. S.,
    2. Araujo M.,
    3. Nieto M. A.
    (1998) Neural induction in whole chick embryo cultures by FGF. Dev. Biol 199, 42–54
    OpenUrlCrossRefPubMedWeb of Science
    1. Alvarez-Otero R.,
    2. Sotelo C.,
    3. Alvarado-Mallart R.-M.
    (1993) Chick/quail chimeras with partial cerebellar grafts: an analysis of the origin and migration of cerebellar cells. J. Comp. Neurol 333, 597–615
    OpenUrlCrossRefPubMedWeb of Science
    1. Ang S. L.,
    2. Rossant J.
    (1993) Anterior mesendoderm induces mouse Engrailed genes in explant cultures. Development 118, 139–149
    OpenUrlAbstract
    1. Arman E.,
    2. Haffner-Krausz R.,
    3. Chen Y.,
    4. Heath J. K.,
    5. Lonai P.
    (1998) Targeted disruption of fibroblast growth factor (FGF) receptor 2 suggests a role for FGF signaling in pregastrulation mammalian development. Proc. Natl. Acad. Sci. USA 95, 5082–5087
    OpenUrlAbstract/FREE Full Text
    1. Bally-Cuif L.,
    2. Alvarado-Mallart R.-M.,
    3. Darnell D. K.,
    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. Bally-Cuif L.,
    2. Wassef M.
    (1994) Ectopic induction and reorganisation of Wnt-1 expression in quail/chick chimeras. Development 120, 3379–3394
    OpenUrlAbstract
    1. Bally-Cuif L.,
    2. Wassef M.
    (1995) Determination events in the nervous system of the vertebrate embryo. Curr. Opin. Genet. Dev 5, 450–458
    OpenUrlCrossRefPubMedWeb of Science
    1. Bally-Cuif L.,
    2. Cholley B.,
    3. Wassef M.
    (1995) Involvement of Wnt-1 in the formation of the mes/metencephalic boundary. Mech. Dev 53, 23–34
    OpenUrlCrossRefPubMedWeb of Science
    1. Bally-Cuif L.,
    2. Gulisano M.,
    3. Broccoli V.,
    4. Boncinelli E.
    (1995) c-otx2 is expressed in two different phases of gastrulation and is sensitive to retinoic acid treatment in chick embryo. Mech Dev 49, 49–63
    OpenUrlCrossRefPubMedWeb of Science
    1. Bloch-Gallego E.,
    2. Millet S.,
    3. Alvarado-Mallart R. M.
    (1996) Further observations on the susceptibility of diencephalic prosomeres to En-2 induction and on the resulting histogenetic capabilities. Mech. Dev 58, 51–63
    OpenUrlCrossRefPubMed
    1. Bueno D.,
    2. Skinner J.,
    3. Abud H.,
    4. Heath J. K.
    (1996) Spatial and temporal relationships between Shh, Fgf4, and Fgf8 gene expression at diverse signalling centers during mouse development. Dev. Dyn 207, 291–299
    OpenUrlCrossRefPubMed
    1. Cheng H. J.,
    2. Flanagan J. G.
    (1994) Identification and cloning of ELF-1, a developmentally expressed ligand for the Mek4 and Sek receptor tyrosine kinases. Cell 79, 157–168
    OpenUrlCrossRefPubMedWeb of Science
    1. Cheng H.-J.,
    2. Nakamoto M.,
    3. Bergemann A. D.,
    4. Flanagan J. D.
    (1995) Complementary gradients in expression and binding of ELF-1 and Mek4 in development of the topographic retinotectal projection map. Cell 82, 371–381
    OpenUrlCrossRefPubMedWeb of Science
    1. Christen B.,
    2. Slack J. M.
    (1997) FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus. Dev. Biol 192, 455–466
    OpenUrlCrossRefPubMed
    1. Crossley P. H.,
    2. Martin G. R.
    (1995) The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo. Development 121, 439–451
    OpenUrlAbstract
    1. Crossley P. H.,
    2. Martinez S.,
    3. Martin G. R.
    (1996) Midbrain development induced by FGF8 in the chick embryo. Nature 380, 66–68
    OpenUrlCrossRefPubMed
    1. Danielian P. S.,
    2. McMahon A. P.
    (1996) Engrailed-1 as a target of the Wnt-1 signalling pathway in vertebrate midbrain development. Nature 383, 332–334
    OpenUrlCrossRefPubMedWeb of Science
    1. Darnell D. K.,
    2. Schoenwolf G. C.
    (1997) Vertical induction of engrailed-2 and other region-specific markers in the early chick embryo. Dev. Dyn 209, 45–58
    OpenUrlCrossRefPubMed
    1. Davis C. A.,
    2. Holmyard D. P.,
    3. Millen K. J.,
    4. Joyner A. J.
    (1991) Examining pattern formation in mouse, chick and frog embryos with an En -specific antiserum. Development 111, 287–298
    OpenUrlAbstract
    1. Deng C.-X.,
    2. Wynshaw-Boris A.,
    3. Shen M.,
    4. Daugherty C.,
    5. Ornitz D.,
    6. Leder P.
    (1994) Murine FGFR-1 is required for early postimplantation growth and axial organisation. Genes Dev 8, 3045–3057
    OpenUrlAbstract/FREE Full Text
    1. Doniach T.
    (1995) Basic FGF as an inducer of anteroposterior neural pattern. Cell 83, 1067–1070
    OpenUrlCrossRefPubMedWeb of Science
    1. Drescher U.,
    2. Kremoser C.,
    3. Handwerker C.,
    4. Loschinger J.,
    5. Noda M.,
    6. Bonhoeffer F.
    (1995) In vitro guidance of retinal ganglion axons by RAGS, a 25kDa tectal protein related to ligands for eph receptor tyrosine kinases. Cell 82, 359–370
    OpenUrlCrossRefPubMedWeb of Science
    1. Dressler G. R.,
    2. Deutsch U.,
    3. Chowdhury K.,
    4. Nornes H. O.,
    5. Gruss P.
    (1990) Pax2, a new murine paired-box-containing gene and its expression in the developing excretory system. Development 109, 787–795
    OpenUrlAbstract/FREE Full Text
    1. Eizema K.,
    2. Koster J. G.,
    3. Stegeman B. I.,
    4. Baarends W. M.,
    5. Lanser P. H.,
    6. Destree O. H.
    (1994) Comparative analysis of Engrailed-1 and Wnt-1 expression in the developing central nervous system of Xenopus laevis. Int. J. Dev. Biol 38, 623–632
    OpenUrlPubMed
    1. Favor J.,
    2. Sandulache R.,
    3. Neuhauser-Klaus A.,
    4. Pretsch W.,
    5. Chatterjee B.,
    6. Senft E.,
    7. Wurst W.,
    8. Blanquet V.,
    9. Grimes P.,
    10. Sporle R.,
    11. Schughart K.
    (1996) The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc. Natl. Acad. Sci. USA 93, 13870–13875
    OpenUrlAbstract/FREE Full Text
    1. Feldman B.,
    2. Poueymirou W.,
    3. Papaioannou V. E.,
    4. DeChiara T. M.,
    5. Goldfarb M.
    (1995) Requirement of FGF-4 for postimplantation mouse development. Science 267, 246–249
    OpenUrlAbstract/FREE Full Text
    1. Friedman G. C.,
    2. O'Leary D. D.
    (1996) Retroviral misexpression of engrailed genes in the chick optic tectum perturbs the topographic targeting of retinal axons. J. Neurosci 16, 5498–5509
    OpenUrlAbstract/FREE Full Text
    1. Fritzsch B.,
    2. Nichols D. H.,
    3. Echelard Y.,
    4. McMahon A. P.
    (1995) Development of midbrain and anterior hindbrain ocular motoneurons in normal and Wnt-1 knockout mice. J. Neurobiol 27, 457–469
    OpenUrlCrossRefPubMedWeb of Science
    1. Gardner C. A.,
    2. Darnell D. K.,
    3. Poole S. J.,
    4. Ordahl C. P.,
    5. Barald K. F.
    (1988) Expression of an engrailed-like gene during development of the early embryonic chick nervous system. J. Neurosci. Res 21, 426–437
    OpenUrlCrossRefPubMedWeb of Science
    1. Gardner C. A.,
    2. Barald K. F.
    (1991) The cellular environment controlsthe expression of engrailed -like protein in the cranial neuroepithelium of quail-chcik chimeric embryos. Development 113, 1037–1048
    OpenUrlAbstract
    1. Gardner C. A.,
    2. Barald K. F.
    (1992) Expression patterns of engrailed-like proteins in the chick embryo. Dev. Dyn 193, 370–388
    OpenUrlPubMed
    1. Hallonet M. E. R.,
    2. Teillet M. A.,
    3. LeDouarin N. M.
    (1990) A new approach to the development of the cerebellum provided by the quail-chick marker system. Development 108, 19–31
    OpenUrlAbstract
    1. Hallonet M. E. R.,
    2. LeDouarin N. M.
    (1993) Tracing neuroepithelial cells of the mesencephalic and metencephalic alar plates during cerebellar ontogeny in quail-chick chimeras. Eur. J. Neurosci 5, 1145–1155
    OpenUrlCrossRefPubMedWeb of Science
    1. Hamburger V.,
    2. Hamilton H.
    (1951) A series of normal stages in the development of the chick embryo. J. Morphol 88, 49–92
    OpenUrlCrossRefPubMedWeb of Science
    1. Hanks M.,
    2. Wurst W.,
    3. Anson-Cartwright L.,
    4. Auerbach A. B.,
    5. Joyner A. L.
    (1995) Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2. Science 269, 679–682
    OpenUrlAbstract/FREE Full Text
    1. Hatta K.,
    2. Bremiller R.,
    3. Westerfield M.,
    4. Kimmel C. B.
    (1991) Diversity of expression of engrailed-like antigens in zebrafish. Development 112, 821–832
    OpenUrlAbstract
    1. Heikinheimo M.,
    2. Lawshe A.,
    3. Shackleford G. M.,
    4. Wilson D. B.,
    5. MacArthur C. A.
    (1994) Fgf-8 expression in the post-gastrulation mouse suggests roles in the development of the face, limbs and central nervous system. Mech. Dev 48, 129–138
    OpenUrlCrossRefPubMedWeb of Science
    1. Heller N.,
    2. Brandli A. W.
    (1997) Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development. Mech. Dev 69, 83–104
    OpenUrlCrossRefPubMedWeb of Science
    1. Hemmati-Brivanlou A.,
    2. Harland R. M.
    (1989) Expression of an engrailed-related protein is induced in the anterior neural ectoderm of early Xenopus embryos. Development 106, 611–7
    OpenUrlAbstract
    1. Hemmati-Brivanlou A.,
    2. Stewart R. M.,
    3. Harland R. M.
    (1990) Region-specific neural induction of an engrailed protein by anterior notochord in Xenopus. Science 250, 800–802
    OpenUrlAbstract/FREE Full Text
    1. Hollyday M.,
    2. McMahon J. A.,
    3. McMahon A. P.
    (1995) Wnt expression patterns in chick embryo nervous system. Mech Dev 52, 9–25
    OpenUrlCrossRefPubMedWeb of Science
    1. Ichijo H.,
    2. Fujita S.,
    3. Matsuno T.,
    4. Nakamura H.
    (1990) Rotation of the tectal primordium reveals plasticity of target recognition in retinotectal projection. Development 110, 331–342
    OpenUrlAbstract/FREE Full Text
    1. Isaacs H. V.,
    2. Tannahill D.,
    3. Slack J. M.
    (1992) Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification. Development 114, 711–20
    OpenUrlAbstract
    1. Itasaki N.,
    2. Ichijo H.,
    3. Hama C.,
    4. Matsuno T.,
    5. Nakamura H.
    (1991) Establishment of rostrocaudal polarity in tectal primordium: engrailed expression and subsequent tectal polarity. Development 113, 1133–44
    OpenUrlAbstract
    1. Itasaki N.,
    2. Nakamura H.
    (1996) A role for gradient en expression in positional specification on the optic tectum. Neuron 16, 55–62
    OpenUrlCrossRefPubMedWeb of Science
    1. Joyner A. L.,
    2. Herrup K.,
    3. Auerbach B. A.,
    4. Davis C. A.,
    5. Rossant J.
    (1991) Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox. Science 251, 1239–1243
    OpenUrlAbstract/FREE Full Text
    1. Joyner A. L.
    (1996) Engrailed, Wnt and Pax genes regulate midbrain-hindbrain development. Trends Genet 12, 15–20
    OpenUrlCrossRefPubMedWeb of Science
    1. Kelly G. M.,
    2. Moon R. T.
    (1995) Involvement of wnt1 and pax2 in the formation of the midbrain-hindbrain boundary in the zebrafish gastrula. Dev. Genet 17, 129–140
    OpenUrlCrossRefPubMedWeb of Science
    1. Krauss S.,
    2. Maden M.,
    3. Holder N.,
    4. Wilson S. W.
    (1992) Zebrafish pax[b] is involved in the formation of the midbrain-hindbrain boundary. Nature 360, 87–89
    OpenUrlCrossRefPubMed
    1. Kuemerle B.,
    2. Zanjani H.,
    3. Joyner A.,
    4. Herrup K.
    (1997) Pattern deformities and cell loss in Engrailed-2 mutant mice suggest two separate patterning events during cerebellar development. J. Neurosci 17, 7881–7889
    OpenUrlAbstract/FREE Full Text
    1. Lee S. M.,
    2. Danielian P. S.,
    3. Fritzsch B.,
    4. McMahon A. P.
    (1997) Evidence that FGF8 signalling from the midbrain-hindbrain junction regulates growth and polarity in the developing midbrain. Development 124, 959–969
    OpenUrlAbstract
    1. Logan C.,
    2. Wizenmann A.,
    3. Drescher U.,
    4. Monschau B.,
    5. Bonhoeffer F.,
    6. Lumsden A.
    (1996) Rostral optic tectum acquires caudal characteristics following ectopic engrailed expression. Curr. Biol 6, 1006–1014
    OpenUrlCrossRefPubMedWeb of Science
    1. Lumsden A. G. S.,
    2. Davies A. M.
    (1983) Earliest sensory nerve fibres are guided to peripheral targets by attractants other than nerve growth factor. Nature 306, 786–788
    OpenUrlCrossRefPubMed
    1. MacArthur C. A.,
    2. Lawshe A.,
    3. Xu J.,
    4. Santos-Ocampo S.,
    5. Heikinheimo M.,
    6. Chellaiah A. T.,
    7. Ornitz D. M.
    (1995) FGF-8 isoforms activate receptor splice forms that are expressed in mesenchymal regions of mouse development. Development 121, 3603–3613
    OpenUrlAbstract
    1. Mahmood R.,
    2. Bresnick J.,
    3. Hornbruch A.,
    4. Mahony K.,
    5. Morton N.,
    6. Colquhoun K.,
    7. Martin P.,
    8. Lumsden A.,
    9. Dickson C.,
    10. Mason I.
    (1995) FGF-8 in the mouse embryo: a role in the initiation and maintenance of limb bud outgrowth. Curr. Biol 5, 797–806
    OpenUrlCrossRefPubMedWeb of Science
    1. Mahmood R.,
    2. Mason I. J.,
    3. Morriss-Kay G. M.
    (1996) Expression of Fgf-3 in relation to hindbrain segmentation, otic pit position and pharyngeal arch morphology in normal and retinoic acid-exposed mouse embryos. Anat. Embryol. (Berl) 194, 13–22
    OpenUrlPubMed
    1. Marin F.,
    2. Puelles L.
    (1994) Patterning of the embryonic midbrain after experimental inversions: a polarizing activity from the isthmus. Dev. Biol 163, 19–37
    OpenUrlCrossRefPubMedWeb of Science
    1. Martinez S.,
    2. Alvarado-Mallart R. M.
    (1989) Rostral cerebellum originates from the caudal portion of the so-called ‘mesencephalic’ vesicle: a study using chick/quail chimeras. Eur. J. Neurosci 1, 549–560
    OpenUrlCrossRefPubMedWeb of Science
    1. Martinez S.,
    2. Alvarado-Mallart R.-M.
    (1990) Expression of the homeobox gene Chick-en in chick/quail chimeras with inverted mes-metencephalic grafts. Dev. Biol 139, 432–436
    OpenUrlCrossRefPubMedWeb of Science
    1. Martinez S.,
    2. Wassef M.,
    3. Alvarado-Mallart R.-M.
    (1991) Induction of a mesencephalic phenotype in the 2-day-old chick prosencephalon is preceded by the early expression of the homeobox gene en. Neuron 6, 971–981
    OpenUrlCrossRefPubMedWeb of Science
    1. Mason I.
    (1996) Neural induction: do FGFs strike a cord?. Curr. Biol 6, 672–675
    OpenUrlCrossRefPubMedWeb of Science
    1. McMahon A. P.,
    2. Bradley A.
    (1990) The wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain. Cell 62, 1073–1085
    OpenUrlCrossRefPubMedWeb of Science
    1. McMahon A. P.,
    2. Joyner A. L.,
    3. Bradley A.,
    4. McMahon J. A.
    (1992). The midbrain-hindbrain phenotype of wnt1 /wnt1 mice results from stepwise deletion of engrailed -expressing cells by 9.5 days postcoitum.. Cell 69, 581–595
    OpenUrlCrossRefPubMedWeb of Science
    1. Meyers E. N.,
    2. Lewandoski M.,
    3. Martin G. R.
    (1998) An Fgf8 mutant allelic series generated by Cre-and Flp-mediated recombination. Nat. Genet 18, 136–141
    OpenUrlCrossRefPubMedWeb of Science
    1. Millen K. J.,
    2. Wurst W.,
    3. Herrup K.,
    4. Joyner A. L.
    (1994) Abnormal embryonic cerebellar development and patterning of postnatal foliation in two mouse Engrailed-2 mutants. Development 120, 695–706
    OpenUrlAbstract
    1. Millen K. J.,
    2. Hui C. C.,
    3. Joyner A. L.
    (1995) A role for En-2 and other murine homologues of Drosophila segment polarity genes in regulating positional information in the developing cerebellum. Development 121, 3935–3945
    OpenUrlAbstract
    1. Millet S.,
    2. Alvarado-Mallart R. M.
    (1995) Expression of the homeobox-containing gene En-2 during the development of the chick central nervous system. Eur. J. Neurosci 7, 777–791
    OpenUrlCrossRefPubMedWeb of Science
    1. Millet S.,
    2. Bloch-Gallego E.,
    3. Simeone A.,
    4. Alvarado-Mallart R. M.
    (1996) The caudal limit of Otx2 gene expression as a marker of the midbrain/hindbrain boundary: a study using in situ hybridisation and chick/quail homotopic grafts. Development 122, 3785–3797
    OpenUrlAbstract
    1. Muhr J.,
    2. Jessell T. M.,
    3. Edlund T.
    (1997) Assignment of early caudal identity to neural plate cells by a signal from caudal paraxial mesoderm. Neuron 19, 487–502
    OpenUrlCrossRefPubMedWeb of Science
    1. Nakamura H.,
    2. Nakano K. E.,
    3. Igawa H. H.,
    4. Takagi S.,
    5. Fujisawa H.
    (1986) Plasticity and rigidity of differentiation of brain vesicles studied in quail-chick chimeras. Cell Diff 19, 187–193
    OpenUrlCrossRefPubMedWeb of Science
    1. Nakamura H.,
    2. Takagi S.,
    3. Tsuji T.,
    4. Matsui K. A.,
    5. Fujisawa H.
    (1988) The prosencephalon has the capacity to differentiate into the optic tectum: analysis in quail-chick-chimeric brains. Dev. Growth Diff 30, 717–725
    OpenUrlCrossRef
    1. Nakamura H.
    (1990) Do CNS anlagen have plasticity in differentiation? Analysis in quail-chick chimera. Brain Res 511, 122–128
    OpenUrlCrossRefPubMed
    1. Niswander L.,
    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. Ohuchi H.,
    2. Yoshioka H.,
    3. Tanaka A.,
    4. Kawakami Y.,
    5. Nohno T.,
    6. Noji S.
    (1994) Involvement of androgen-induced growth factor (FGF-8) gene in mouse embryogenesis and morphogenesis. Biochem. Biophys. Res. Commun 204, 882–888
    OpenUrlCrossRefPubMedWeb of Science
    1. Parr B. A.,
    2. Shea M. J.,
    3. Vassileva G.,
    4. McMahon A. P.
    (1993) Mouse wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds. Development 119, 247–261
    OpenUrlAbstract
    1. Puschel A. W.,
    2. Westerfield M.,
    3. Dressler G. R.
    (1992) Comparative analysis of Pax-2 protein distributions during neurulation in mice and zebrafish. Mech Dev 38, 197–208
    OpenUrlCrossRefPubMedWeb of Science
    1. Riefers F.,
    2. Bohli H.,
    3. Walsh E.,
    4. Crossley P.,
    5. Stanier D.,
    6. Brand M.
    (1998) Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis. Development 125, 2381–2395
    OpenUrlAbstract
    1. Rhinn M.,
    2. Dierich A.,
    3. Shawlot W.,
    4. Behringer R. R.,
    5. Le Meur M.,
    6. Ang S. L.
    (1998) Sequential roles for Otx2 in visceral endoderm and neuroectoderm for forebrain and midbrain induction and specification. Development 125, 845–856
    OpenUrlAbstract
    1. Roberts C.,
    2. Platt N.,
    3. Streit A.,
    4. Schachner M.,
    5. Stern C. D.
    (1991) The L5 epitope: an early marker for neural induction in the chick embryo and its involvement in inductive interactions. Development 112, 959–970
    OpenUrlAbstract
    1. Rowitch D. H.,
    2. McMahon A. P.
    (1995) Pax-2 expression in the murine neural plate precedes and encompasses the expression domains of Wnt-1 and En-1. Mech Dev 52, 3–8
    OpenUrlCrossRefPubMedWeb of Science
    1. Ruiz i Altaba A.
    (1994) Pattern formation in the vertebrate neural plate. Trends Neurosci 17, 233–243
    OpenUrlCrossRefPubMedWeb of Science
    1. Ruiz i Altaba A.
    (1998) Neural patterning. Deconstructing the organizer. Nature 391, 748–749
    OpenUrlCrossRefPubMed
    1. Schoenwolf G. C.,
    2. Sheard P.
    (1990) Fate mapping the avian epiblast with focal injections of a fluorescent-histochemical marker: ectodermal derivatives. J. Exp. Zool 255, 323–339
    OpenUrlCrossRefPubMedWeb of Science
    1. Schwarz M.,
    2. Alvarez-Bolado G.,
    3. Urbanek P.,
    4. Busslinger M.,
    5. Gruss P.
    (1997) Conserved biological function between Pax-2 and Pax-5 in midbrain and cerebellum development: evidence from targeted mutations. Proc. Natl. Acad. Sci. USA 94, 14518–1423
    OpenUrlAbstract/FREE Full Text
    1. Shamim H.,
    2. Mason I.
    (1998) Expression of Gbx-2 during early development of the chick embryo. Mech. Dev 76, 157–159
    OpenUrlCrossRefPubMedWeb of Science
    1. Storey K. G.,
    2. Goriely A.,
    3. Sargent C. M.,
    4. Brown J. M.,
    5. Burns H. D.,
    6. Abud H. M.,
    7. Heath J. K.
    (1998) Early posterior neural tissue is induced by FGF in the chick embryo. Development 125, 473–484
    OpenUrlAbstract
    1. Thomas K. R.,
    2. Capecchi M. R.
    (1990) Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development. Nature 346, 847–850
    OpenUrlCrossRefPubMedWeb of Science
    1. Thomas K. R.,
    2. Musci T. S.,
    3. Neumann P. E.,
    4. Capecchi M. R.
    (1991) Swaying is a mutant allele of the proto-oncogene wnt-1. Cell 67, 969–976
    OpenUrlCrossRefPubMedWeb of Science
    1. Urbanek P.,
    2. Fetka I.,
    3. Meisler M. H.,
    4. Busslinger M.
    (1997) Cooperation of Pax2 and Pax5 in midbrain and cerebellum development. Proc. Natl. Acad. Sci. USA 94, 5703–5708
    OpenUrlAbstract/FREE Full Text
    1. Urbanek P.,
    2. Wang Z. Q.,
    3. Fetka I.,
    4. Wagner E. F.,
    5. Busslinger M.
    (1994) Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP. Cell 79, 901–912
    OpenUrlCrossRefPubMedWeb of Science
    1. Vogel A.,
    2. Rodriguez C.,
    3. Izpisua-Belmonte J. C.
    (1996) Involvement of FGF-8 in initiation, outgrowth and patterning of the vertebrate limb. Development 122, 1737–1750
    OpenUrlAbstract
    1. Wassarman K. M.,
    2. Lewandoski M.,
    3. Campbell K.,
    4. Joyner A. L.,
    5. Rubenstein J. L.,
    6. Martinez S.,
    7. Martin G. R.
    (1997) Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function. Development 124, 2923–2934
    OpenUrlAbstract
    1. Wassef M.,
    2. Joyner A. L.
    (1997) Early mesencephalon/metencephalon patterning and development of the cerebellum. Perspect. Dev. Neurobiol 5, 3–16
    OpenUrlPubMedWeb of Science
    1. Wilkinson D. G.,
    2. Bailes J. A.,
    3. McMahon A. P.
    (1987) Expression of the proto-oncogene wnt-1 is restricted to specific neural cells in the developing mouse embryo. Cell 50, 79–88
    OpenUrlCrossRefPubMedWeb of Science
    1. Williams E. J.,
    2. Furness J.,
    3. Walsh F. S.,
    4. Doherty P.
    (1994) Activation of the FGF receptor underlies neurite outgrowth stimulated by L1, N-CAM, and N-cadherin. Neuron 13, 583–594
    OpenUrlCrossRefPubMedWeb of Science
    1. Wurst W.,
    2. Auerbach A. B.,
    3. Joyner A. L.
    (1994) Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum. Development 120, 2065–2075
    OpenUrlAbstract
    1. Yamaguchi T.,
    2. Harpal K.,
    3. Henkemeyer M.,
    4. Rossant J.
    (1994) fgfr-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation. Genes Dev 8, 3032–3044
    OpenUrlAbstract/FREE Full Text
    1. Ye W.,
    2. Shimamura K.,
    3. Rubenstein J. R.,
    4. Hynes M. A.,
    5. Rosenthal A.
    (1998) FGF and Shh signals control dopaminergic and serotonergic cell fate in the anterior neural plate. Cell 93, 755–766
    OpenUrlCrossRefPubMedWeb of Science
Previous ArticleNext Article
Back to top
Previous ArticleNext Article

This Issue

 Download PDF

Email

Thank you for your interest in spreading the word on Development.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain
(Your Name) has sent you a message from Development
(Your Name) thought you would like to see the Development web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
JOURNAL ARTICLES
Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain
H. Shamim, R. Mahmood, C. Logan, P. Doherty, A. Lumsden, I. Mason
Development 1999 126: 945-959;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
JOURNAL ARTICLES
Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain
H. Shamim, R. Mahmood, C. Logan, P. Doherty, A. Lumsden, I. Mason
Development 1999 126: 945-959;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Alerts

Please log in to add an alert for this article.

Sign in to email alerts with your email address

Article navigation

  • Top
  • Article
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice
  • REF-1, a protein with two bHLH domains, alters the pattern of cell fusion in C. elegans by regulating Hox protein activity
  • Centrosome migration into the Drosophila oocyte is independent of BicD and egl, and of the organisation of the microtubule cytoskeleton
Show more JOURNAL ARTICLES

Similar articles

Other journals from The Company of Biologists

Journal of Cell Science

Journal of Experimental Biology

Disease Models & Mechanisms

Biology Open

Advertisement

An interview with Swathi Arur

Swathi Arur joined the team at Development as an Academic Editor in 2020. Her lab uses multidisciplinary approaches to understand female germline development and fertility. We met with her over Zoom to hear more about her life, her career and her love for C. elegans.


Jim Wells and Hanna Mikkola join our team of Editors

We are pleased to welcome James (Jim) Wells and Hanna Mikkola to our team of Editors. Jim joins us a new Academic Editor, taking over from Gordan Keller, and Hanna joins our team of Associate Editors. Find out more about their research interests and areas of expertise.


New funding scheme supports sustainable events

As part of our Sustainable Conferencing Initiative, we are pleased to announce funding for organisers that seek to reduce the environmental footprint of their event. The next deadline to apply for a Scientific Meeting grant is 26 March 2021.


Read & Publish participation continues to grow

“I’d heard of Read & Publish deals and knew that many universities, including mine, had signed up to them but I had not previously understood the benefits that these deals bring to authors who work at those universities.”

Professor Sally Lowell (University of Edinburgh) shares her experience of publishing Open Access as part of our growing Read & Publish initiative. We now have over 150 institutions in 15 countries and four library consortia taking part – find out more and view our full list of participating institutions.


Upcoming special issues

Imaging Development, Stem Cells and Regeneration
Submission deadline: 30 March 2021
Publication: mid-2021

The Immune System in Development and Regeneration
Guest editors: Florent Ginhoux and Paul Martin
Submission deadline: 1 September 2021
Publication: Spring 2022

Both special issues welcome Review articles as well as Research articles, and will be widely promoted online and at key global conferences.


Development presents...

Our successful webinar series continues into 2021, with early-career researchers presenting their papers and a chance to virtually network with the developmental biology community afterwards. Here, Brandon Carpenter talks about how inherited histone methylation defines the germline versus soma decision in C. elegans. 

Sign up to join our next session:

10 March
Time: TBC
Chaired by: Thomas Lecuit

Articles

  • Accepted manuscripts
  • Issue in progress
  • Latest complete issue
  • Issue archive
  • Archive by article type
  • Special issues
  • Subject collections
  • Sign up for alerts

About us

  • About Development
  • About the Node
  • Editors and board
  • Editor biographies
  • Travelling Fellowships
  • Grants and funding
  • Journal Meetings
  • Workshops
  • The Company of Biologists

For authors

  • Submit a manuscript
  • Aims and scope
  • Presubmission enquiries
  • Article types
  • Manuscript preparation
  • Cover suggestions
  • Editorial process
  • Promoting your paper
  • Open Access
  • Biology Open transfer

Journal info

  • Journal policies
  • Rights and permissions
  • Media policies
  • Reviewer guide
  • Sign up for alerts

Contact

  • Contact Development
  • Subscriptions
  • Advertising
  • Feedback
  • Institutional usage stats (logged-in users only)

 Twitter   YouTube   LinkedIn

© 2021   The Company of Biologists Ltd   Registered Charity 277992