Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation.

In an expression cloning screen in Xenopus embryos, we identified a gene that when overexpressed expanded the neural plate at the expense of adjacent neural crest and epidermis. This gene, which we named geminin, had no sequence similarity to known gene families. We later discovered that geminin's neuralizing domain was part of a bifunctional protein whose C-terminal coiled-coil domain may play a role in regulating DNA replication. We report here on the neuralizing function of geminin. The localization, effect of misexpression and activity of a dominant negative geminin suggest that the product of this gene has an essential early role in specifying neural cell fate in vertebrates. Maternal geminin mRNA is found throughout the animal hemisphere from oocyte through late blastula. At the early gastrula, however, expression is restricted to a dorsal ectodermal territory that prefigures the neural plate. Misexpression of geminin in gastrula ectoderm suppresses BMP4 expression and converts prospective epidermis into neural tissue. In ectodermal explants, geminin induces expression of the early proneural gene neurogenin-related 1 although not itself being induced by that gene. Later, embryos expressing geminin have an expanded dorsal neural territory and ventral ectoderm is converted to neurons. A putative dominant negative geminin lacking the neuralizing domain suppresses neural differentiation and, when misexpressed dorsally, produces islands of epidermal gene expression within the neurectodermal territory, effects that are rescued by coexpression of the full-length molecule. Taken together, these data indicate that geminin plays an early role in establishing a neural domain during gastrulation.

[1]  D. Wilkinson In situ hybridization: a practical approach , 1998 .

[2]  N. Ueno,et al.  Xenopus msx1 mediates epidermal induction and neural inhibition by BMP4. , 1997, Development.

[3]  R. Morgan,et al.  The role in neural patterning of translation initiation factor eIF4AII; induction of neural fold genes. , 1997, Development.

[4]  J. Johnson,et al.  XATH-1, a vertebrate homolog of Drosophila atonal, induces a neuronal differentiation within ectodermal progenitors. , 1997, Developmental biology.

[5]  A. Hemmati‐Brivanlou,et al.  Neural induction in Xenopus laevis: evidence for the default model , 1997, Current Opinion in Neurobiology.

[6]  Y. Sasai,et al.  Ectodermal patterning in vertebrate embryos. , 1997, Developmental biology.

[7]  Jacqueline E. Lee Basic helix-loop-helix genes in neural development , 1997, Current Opinion in Neurobiology.

[8]  R. Kageyama,et al.  Conversion of ectoderm into a neural fate by ATH‐3, a vertebrate basic helix–loop–helix gene homologous to Drosophila proneural gene atonal , 1997, The EMBO journal.

[9]  William C. Smith,et al.  Direct neural induction and selective inhibition of mesoderm and epidermis inducers by Xnr3. , 1997, Development.

[10]  W. Harris,et al.  Xenopus Pax-6 and retinal development. , 1997, Journal of neurobiology.

[11]  J. Gerhart,et al.  Formation and function of Spemann's organizer. , 1997, Annual review of cell and developmental biology.

[12]  B. Biehs,et al.  The Drosophila decapentaplegic and short gastrulation genes function antagonistically during adult wing vein development. , 1996, Development.

[13]  M. Kirschner,et al.  Expression cloning of a Xenopus T-related gene (Xombi) involved in mesodermal patterning and blastopore lip formation. , 1996, Development.

[14]  David J. Anderson,et al.  Identification of neurogenin, a Vertebrate Neuronal Determination Gene , 1996, Cell.

[15]  M. Kirschner,et al.  A Xenopus nodal-related gene that acts in synergy with noggin to induce complete secondary axis and notochord formation. , 1996, Development.

[16]  K. Kroll,et al.  Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation. , 1996, Development.

[17]  R. Harland,et al.  The Spemann Organizer Signal noggin Binds and Inactivates Bone Morphogenetic Protein 4 , 1996, Cell.

[18]  Y. Sasai,et al.  Dorsoventral Patterning in Xenopus: Inhibition of Ventral Signals by Direct Binding of Chordin to BMP-4 , 1996, Cell.

[19]  J. Smith,et al.  Xom: a Xenopus homeobox gene that mediates the early effects of BMP-4. , 1996, Development.

[20]  G. von Dassow,et al.  Regulation of dorsal-ventral patterning: the ventralizing effects of the novel Xenopus homeobox gene Vox. , 1996, Development.

[21]  Ruth Díez del Corral,et al.  araucan and caupolican, Two Members of the Novel Iroquois Complex, Encode Homeoproteins That Control Proneural and Vein-Forming Genes , 1996, Cell.

[22]  誠 浅島,et al.  Whole mount in situ hybridization , 1996 .

[23]  R. Harland,et al.  Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern. , 1995, Development.

[24]  H. Okamoto,et al.  bFGF as a possible morphogen for the anteroposterior axis of the central nervous system in Xenopus. , 1995, Development.

[25]  B. Berger,et al.  Predicting coiled coils by use of pairwise residue correlations. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[26]  P. Wilson,et al.  Induction of epidermis and inhibition of neural fate by Bmp-4 , 1995, Nature.

[27]  J. Smith,et al.  Osteogenic protein-1 binds to activin type II receptors and induces certain activin-like effects , 1995, The Journal of cell biology.

[28]  David Ish-Horowicz,et al.  Primary neurogenesis in Xenopus embryos regulated by a homologue of the Drosophila neurogenic gene Delta , 1995, Nature.

[29]  P. Good,et al.  Dorsal-ventral patterning and differentiation of noggin-induced neural tissue in the absence of mesoderm. , 1995, Development.

[30]  H. Weintraub,et al.  Conversion of Xenopus ectoderm into neurons by NeuroD, a basic helix-loop-helix protein. , 1995, Science.

[31]  P. Lemaire,et al.  Expression cloning of Siamois, a xenopus homeobox gene expressed in dorsal-vegetal cells of blastulae and able to induce a complete secondary axis , 1995, Cell.

[32]  V. Agarwal,et al.  XIPOU 2, a noggin-inducible gene, has direct neuralizing activity. , 1995, Development.

[33]  M. Bronner‐Fraser,et al.  Origins of the avian neural crest: the role of neural plate-epidermal interactions. , 1995, Development.

[34]  A. Chitnis,et al.  Neural induction and neurogenesis in amphibian embryos. , 1995, Perspectives on developmental neurobiology.

[35]  G. Thomsen,et al.  Ventral mesodermal patterning in Xenopus embryos: expression patterns and activities of BMP-2 and BMP-4. , 1995, Developmental genetics.

[36]  Y. Sasai,et al.  Xenopus chordin: A novel dorsalizing factor activated by organizer-specific homeobox genes , 1994, Cell.

[37]  W. Harris,et al.  XASH genes promote neurogenesis in Xenopus embryos. , 1994, Development.

[38]  Douglas A. Melton,et al.  Mesodermal patterning by an inducer gradient depends on secondary cell–cell communication , 1994, Current Biology.

[39]  R. Harland Neural induction in Xenopus. , 1994, Current opinion in genetics & development.

[40]  H. Weintraub,et al.  Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate. , 1994, Genes & development.

[41]  Y. Rao Conversion of a mesodermalizing molecule, the Xenopus Brachyury gene, into a neuralizing factor. , 1994, Genes & development.

[42]  R. Harland,et al.  Neural induction by the secreted polypeptide noggin. , 1993, Science.

[43]  J. Shih,et al.  XASH-3, a novel Xenopus achaete-scute homolog, provides an early marker of planar neural induction and position along the mediolateral axis of the neural plate. , 1993, Development.

[44]  William C. Smith,et al.  Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos , 1992, Cell.

[45]  N. Ueno,et al.  Genes for bone morphogenetic proteins are differentially transcribed in early amphibian embryos. , 1992, Biochemical and biophysical research communications.

[46]  B. Hogan,et al.  DVR-4 (bone morphogenetic protein-4) as a posterior-ventralizing factor in Xenopus mesoderm induction. , 1992, Development.

[47]  D. Wilkinson Wholemount in situ hybridization of vertebrate embryos , 1992 .

[48]  K. Richter,et al.  Localization of a nervous system-specific class II beta-tubulin gene in Xenopus laevis embryos by whole-mount in situ hybridization. , 1991, The International journal of developmental biology.

[49]  R. Harland,et al.  Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center , 1991, Cell.

[50]  A. Lupas,et al.  Predicting coiled coils from protein sequences , 1991, Science.

[51]  W. Harris,et al.  Neuronal determination without cell division in xenopus embryos , 1991, Neuron.

[52]  H. Peng Solutions and protocols , 1991 .

[53]  R. Harland,et al.  In situ hybridization: an improved whole-mount method for Xenopus embryos. , 1991, Methods in cell biology.

[54]  A. Jacobson,et al.  The origins of neural crest cells in the axolotl. , 1990, Developmental biology.

[55]  L. Tacke,et al.  Neural differentiation of Xenopus laevis ectoderm takes place after disaggregation and delayed reaggregation without inducer. , 1989, Cell differentiation and development : the official journal of the International Society of Developmental Biologists.

[56]  J. Gurdon,et al.  A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest , 1989, Cell.

[57]  J. Slack,et al.  Clonal analysis of mesoderm induction in Xenopus laevis. , 1989, Developmental biology.

[58]  I. Dawid,et al.  Gene expression in the embryonic nervous system of Xenopus laevis. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[59]  D. Melton,et al.  In vitro RNA synthesis with SP6 RNA polymerase. , 1987, Methods in enzymology.

[60]  I. Dawid,et al.  Epidermal keratin gene expressed in embryos of Xenopus laevis. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[61]  Kurt E. Johnson,et al.  Normal Table of Xenopus Laevis , 1968, The Yale Journal of Biology and Medicine.

[62]  J. Gurdon The Effects of Ultraviolet Irradiation on Uncleaved Eggs of Xenopus Laevis , 1960 .