Literature DB >> 9315901

Expression patterns of developmental control genes in normal and Engrailed-1 mutant mouse spinal cord reveal early diversity in developing interneurons.

M P Matise1, A L Joyner.   

Abstract

The vertebrate spinal cord has long served as a useful system for studying the pattern of cell differentiation along the dorsoventral (d/v) axis. In this paper, we have defined the expression of several classes of genes expressed in restricted d/v domains in the intermediate region (IR) of the mouse spinal cord, in which most interneurons are generated. From this analysis, we have found that spinal cord interneurons and their precursors express unique combinations of transcription factors and Notch ligands at the onset of their differentiation. The domains of expression of a number of different classes of genes share similar boundaries, indicating that there could be a basic subdivision of the ventral IR into four distinct regions. This differential gene expression suggests that spinal cord interneurons acquire unique identities early in their development and that Notch signaling mechanisms may participate in the determination of cell fate along the d/v axis. Gene expression studies in Engrailed-1 (En-1) mutants showed that En-1-expressing and other closely positioned classes of neurons do not require the homeodomain protein En-1 for their early pattern of differentiation. Rather, it is suggested that En-1 may function to distinguish a subset of interneurons during the later maturation of the spinal cord.

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Year:  1997        PMID: 9315901      PMCID: PMC6793918     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  45 in total

1.  Expression during embryogenesis of a mouse gene with sequence homology to the Drosophila engrailed gene.

Authors:  A L Joyner; T Kornberg; K G Coleman; D R Cox; G R Martin
Journal:  Cell       Date:  1985-11       Impact factor: 41.582

2.  Expression patterns of Jagged, Delta1, Notch1, Notch2, and Notch3 genes identify ligand-receptor pairs that may function in neural development.

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Journal:  Mol Cell Neurosci       Date:  1996       Impact factor: 4.314

3.  Neurogenesis in spinal cord of mouse: an autoradiographic analysis.

Authors:  H O Nornes; M Carry
Journal:  Brain Res       Date:  1978-12-22       Impact factor: 3.252

4.  The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis.

Authors:  M K Lee; J B Tuttle; L I Rebhun; D W Cleveland; A Frankfurter
Journal:  Cell Motil Cytoskeleton       Date:  1990

5.  A family of mammalian Fringe genes implicated in boundary determination and the Notch pathway.

Authors:  S H Johnston; C Rauskolb; R Wilson; B Prabhakaran; K D Irvine; T F Vogt
Journal:  Development       Date:  1997-06       Impact factor: 6.868

6.  Monoclonal antibody to 5-bromo- and 5-iododeoxyuridine: A new reagent for detection of DNA replication.

Authors:  H G Gratzner
Journal:  Science       Date:  1982-10-29       Impact factor: 47.728

7.  Spatially and temporally restricted expression of Pax2 during murine neurogenesis.

Authors:  H O Nornes; G R Dressler; E W Knapik; U Deutsch; P Gruss
Journal:  Development       Date:  1990-08       Impact factor: 6.868

8.  Pax2, a new murine paired-box-containing gene and its expression in the developing excretory system.

Authors:  G R Dressler; U Deutsch; K Chowdhury; H O Nornes; P Gruss
Journal:  Development       Date:  1990-08       Impact factor: 6.868

9.  Dorsal-ventral patterning and differentiation of noggin-induced neural tissue in the absence of mesoderm.

Authors:  A K Knecht; P J Good; I B Dawid; R M Harland
Journal:  Development       Date:  1995-06       Impact factor: 6.868

10.  Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta.

Authors:  B Bettenhausen; M Hrabĕ de Angelis; D Simon; J L Guénet; A Gossler
Journal:  Development       Date:  1995-08       Impact factor: 6.868

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  37 in total

Review 1.  Spinal interneuronal systems: identification, multifunctional character and reconfigurations in mammals.

Authors:  E Jankowska
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

2.  Two lineage boundaries coordinate vertebrate apical ectodermal ridge formation.

Authors:  R A Kimmel; D H Turnbull; V Blanquet; W Wurst; C A Loomis; A L Joyner
Journal:  Genes Dev       Date:  2000-06-01       Impact factor: 11.361

3.  Renshaw cell interneuron specialization is controlled by a temporally restricted transcription factor program.

Authors:  Floor J Stam; Timothy J Hendricks; Jingming Zhang; Eric J Geiman; Cedric Francius; Patricia A Labosky; Frederic Clotman; Martyn Goulding
Journal:  Development       Date:  2011-11-24       Impact factor: 6.868

4.  Role of canonical Wnt signaling/ß-catenin via Dermo1 in cranial dermal cell development.

Authors:  Thu H Tran; Andrew Jarrell; Gabriel E Zentner; Adrienne Welsh; Isaac Brownell; Peter C Scacheri; Radhika Atit
Journal:  Development       Date:  2010-10-27       Impact factor: 6.868

5.  Identification of cerebellin2 in chick and its preferential expression by subsets of developing sensory neurons and their targets in the dorsal horn.

Authors:  Mao Yang; Michael C Cagle; Marcia G Honig
Journal:  J Comp Neurol       Date:  2010-07-15       Impact factor: 3.215

6.  Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus.

Authors:  Aurore Thélie; Simon Desiderio; Julie Hanotel; Ian Quigley; Benoit Van Driessche; Anthony Rodari; Mark D Borromeo; Sadia Kricha; François Lahaye; Jenifer Croce; Gustavo Cerda-Moya; Jesús Ordoño Fernandez; Barbara Bolle; Katharine E Lewis; Maike Sander; Alessandra Pierani; Michael Schubert; Jane E Johnson; Christopher R Kintner; Tomas Pieler; Carine Van Lint; Kristine A Henningfeld; Eric J Bellefroid; Claude Van Campenhout
Journal:  Development       Date:  2015-10-01       Impact factor: 6.868

7.  Renshaw cells and Ia inhibitory interneurons are generated at different times from p1 progenitors and differentiate shortly after exiting the cell cycle.

Authors:  Ana Benito-Gonzalez; Francisco J Alvarez
Journal:  J Neurosci       Date:  2012-01-25       Impact factor: 6.167

8.  Postnatal phenotype and localization of spinal cord V1 derived interneurons.

Authors:  Francisco J Alvarez; Philip C Jonas; Tamar Sapir; Robert Hartley; Maria C Berrocal; Eric J Geiman; Andrew J Todd; Martyn Goulding
Journal:  J Comp Neurol       Date:  2005-12-12       Impact factor: 3.215

9.  Genetic subdivision of the tectum and cerebellum into functionally related regions based on differential sensitivity to engrailed proteins.

Authors:  Sema K Sgaier; Zhimin Lao; Melissa P Villanueva; Frada Berenshteyn; Daniel Stephen; Rowena K Turnbull; Alexandra L Joyner
Journal:  Development       Date:  2007-06       Impact factor: 6.868

10.  En1 is necessary for survival of neurons in the ventral nuclei of the lateral lemniscus.

Authors:  Stefanie C Altieri; Tianna Zhao; Walid Jalabi; Rita R Romito-DiGiacomo; Stephen M Maricich
Journal:  Dev Neurobiol       Date:  2016-04-05       Impact factor: 3.964

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