Inductive signal and tissue responsiveness defining the tectum and the cerebellum.

The mes/metencephalic boundary (isthmus) has an organizing activity for mesencephalon and metencephalon. The candidate signaling molecule is Fgf8 whose mRNA is localized in the region where the cerebellum differentiates. Responding to this signal, the cerebellum differentiates in the metencephalon and the tectum differentiates in the mesencephalon. Based on the assumption that strong Fgf8 signal induces the cerebellum and that the Fgf8b signal is stronger than that of Fgf8a, we carried out experiments to misexpress Fgf8b and Fgf8a in chick embryos. Fgf8a did not affect the expression pattern of Otx2, Gbx2 or Irx2. En2 expression was upregulated in the mesencephalon and in the diencephalon by Fgf8a. Consequently, Fgf8a misexpression resulted in the transformation of the presumptive diencephalon to the fate of the mesencephalon. In contrast, Fgf8b repressed Otx2 expression, but upregulated Gbx2 and Irx2 expression in the mesencephalon. As a result, Fgf8b completely changed the fate of the mesencephalic alar plate to cerebellum. Quantitative analysis showed that Fgf8b signal is 100 times stronger than Fgf8a signal. Co-transfection of Fgf8b with Otx2 indicates that Otx2 is a key molecule in mesencephalic generation. We have shown by RT-PCR that both Fgf8a and Fgf8b are expressed, Fgf8b expression prevailing in the isthmic region. The results all support our working hypothesis that the strong Fgf8 signal induces the neural tissue around the isthmus to differentiate into the cerebellum.

[1]  C. Irving,et al.  Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression. , 2000, Development.

[2]  Harukazu Nakamura,et al.  A Role for Gradient en Expression in Positional Specification on the Optic Tectum , 1996, Neuron.

[3]  K. Losos,et al.  FGF8 can activate Gbx2 and transform regions of the rostral mouse brain into a hindbrain fate. , 1999, Development.

[4]  I. Cobos,et al.  FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. , 1999, Development.

[5]  G. Martin,et al.  An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination , 1998, Nature Genetics.

[6]  N. Itoh,et al.  Involvement of fibroblast growth factor (FGF)18-FGF8 signaling in specification of left-right asymmetry and brain and limb development of the chick embryo , 2000, Mechanisms of Development.

[7]  Wolfgang Wurst,et al.  The caudal limit of Otx2 expression positions the isthmic organizer , 1999, Nature.

[8]  A. Simeone,et al.  Fgf8 and Gbx2 induction concomitant with Otx2 repression is correlated with midbrain-hindbrain fate of caudal prosencephalon. , 1999, Development.

[9]  A. Simeone,et al.  Positioning the isthmic organizer where Otx2 and Gbx2meet. , 2000, Trends in genetics : TIG.

[10]  M. Hatten,et al.  The role of the rhombic lip in avian cerebellum development. , 1999, Development.

[11]  Salvador Martinez,et al.  Midbrain development induced by FGF8 in the chick embryo , 1996, Nature.

[12]  H. Nakamura,et al.  Regulation of the neural crest cell fate by N-myc: promotion of ventral migration and neuronal differentiation. , 1997, Development.

[13]  Harukazu Nakamura Regionalization of the optic tectum: combinations of gene expression that define the tectum , 2001, Trends in Neurosciences.

[14]  G. Martin,et al.  The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo. , 1995, Development.

[15]  K. Umesono,et al.  Efficient targeting of gene expression in chick embryos by microelectroporation , 1999, Development, growth & differentiation.

[16]  D A Kane,et al.  Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain. , 1996, Development.

[17]  H. Ohuchi,et al.  Role of Pax‐5 in the regulation of a mid‐hindbrain organizer’s activity , 1999, Development, growth & differentiation.

[18]  A. Joyner,et al.  Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum. , 1994, Development.

[19]  H. Nakamura,et al.  Pax6 defines the di-mesencephalic boundary by repressing En1 and Pax2. , 2000, Development.

[20]  Viktor Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.

[21]  S. Martinez,et al.  Transplanted mesencephalic quail cells colonize selectively all primary visual nuclei of chick diencephalon: a study using heterotopic transplants. , 1989, Brain research. Developmental brain research.

[22]  M. Brand,et al.  Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function. , 1998, Development.

[23]  G. Arbuthnott Fundamental Neuroscience edited by M.J. Zigmond, F.E. Bloom, S.C. Landis, J.L. Roberts and L.R. Squire , 2000, Trends in Neurosciences.

[24]  A. Joyner,et al.  Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2. , 1995, Science.

[25]  M. Wassef,et al.  Induction of a mesencephalic phenotype in the 2-day-old chick prosencephalon is preceded by the early expression of the homeobox gene en , 1991, Neuron.

[26]  A. McMahon,et al.  Evidence that FGF8 signalling from the midbrain-hindbrain junction regulates growth and polarity in the developing midbrain. , 1997, Development.

[27]  Harukazu Nakamura,et al.  Rostrocaudal polarity of the tectum in birds: Correlation of en gradient and topographic order in retinotectal projection , 1992, Neuron.

[28]  C. MacArthur,et al.  FGF-8 isoforms activate receptor splice forms that are expressed in mesenchymal regions of mouse development. , 1995, Development.

[29]  J. Funahashi,et al.  Misexpression of genes in brain vesicles by in ovo electroporation , 2000, Development, growth & differentiation.

[30]  C. MacArthur,et al.  Genomic structure, mapping, activity and expression of fibroblast growth factor 17 , 1999, Mechanisms of Development.

[31]  B. Hogan,et al.  Comparison of the expression of three highly related genes, Fgf8, Fgf17 and Fgf18, in the mouse embryo , 1998, Mechanisms of Development.

[32]  Alexandra L. Joyner,et al.  A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer , 1999, Nature.

[33]  L. Puelles,et al.  Induction of ectopic engrailed expression and fate change in avian rhombomeres: intersegmental boundaries as barriers , 1995, Mechanisms of Development.

[34]  M. Wassef,et al.  Involvement of Wnt-1 in the formation of the mes/metencephalic boundary , 1995, Mechanisms of Development.

[35]  I. Cobos,et al.  FGF 8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx 2 expression , 1999 .

[36]  M. Brand,et al.  Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis. , 1998, Development.

[37]  D. Ornitz,et al.  Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures. , 2000, Development.

[38]  H. Nakamura,et al.  Plasticity and rigidity of differentiation of brain vesicles studied in quail-chick chimeras. , 1986, Cell differentiation.

[39]  S. Sugiyama,et al.  Interaction between Otx2 and Gbx2 defines the organizing center for the optic tectum , 2000, Mechanisms of Development.

[40]  H. Nakamura,et al.  Pax6 defines the di-mesencephalic boundary by repressing En1 and Pax2. , 2000, Development.

[41]  N. Itasaki,et al.  Expression of en in the Prosencephalon Heterotopically Transplanted into the Mesencephalon , 1992, Development, growth & differentiation.

[42]  H. Nakamura,et al.  Roles of Pax-2 in initiation of the chick tectal development. , 1999, Brain research. Developmental brain research.

[43]  N. Nakatsuji,et al.  A mouse embryonic stem cell line showing pluripotency of differentiation in early embryos and ubiquitous beta-galactosidase expression. , 1990, Cell differentiation and development : the official journal of the International Society of Developmental Biologists.

[44]  Stephen W. Wilson,et al.  Zebrafish pax[b] is involved in the formation of the midbrain–hindbrain boundary , 1992, Nature.

[45]  W. Cowan,et al.  The development of the chick optic tectum. I. Normal morphology and cytoarchitectonic development. , 1971, Brain research.

[46]  P. Doherty,et al.  Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain. , 1999, Development.

[47]  C. MacArthur,et al.  FGF-8 isoforms differ in NIH3T3 cell transforming potential. , 1995, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[48]  H. Nakamura,et al.  Engrailed defines the position of dorsal di-mesencephalic boundary by repressing diencephalic fate. , 1999, Development.