Literature DB >> 8946055

Identification and characterization of novel developmentally regulated proteins in rat spinal cord.

D H Geschwind1, G M Kelly, H Fryer, H Feeser-Bhatt, S Hockfield.   

Abstract

We previously used 2-dimensional (2-D) gel electrophoresis to identify novel proteins that may be involved in the genesis of the mammalian nervous system [1]. Several novel proteins that were up- or down-regulated coincident with neurogenesis and neuronal migration in rat neocortex were identified. To further investigate the expression of some of these developmentally regulated proteins during a comparable period in spinal cord development, 2-D electrophoresis is used to study their regulation in the crude membrane and soluble fractions of spinal cord at embryonic day 12 (E12) and embryonic day 21 (E21). This analysis indicates that 7 of the proteins that exhibited large changes in their synthesis in cerebral cortex between embryonic day 14 (E14) and embryonic day 21 (E21) demonstrate similar up- or down-regulation during spinal cord neurogenesis. However, two proteins are restricted in their expression or developmental regulation. One of these, 667-800, appears cortex-specific, while the up-regulation of protein SC.1 appears to be spinal cord specific. Several of these proteins also appear to be enriched in both the cortex and spinal cord relative to non-neural tissues (117, 162, 182, 310 [TOAD-64], 667-800) and may be neural specific. To further characterize its expression, one of these neural-specific, up-regulated proteins, TOAD-64 (protein 310) [2-4], is studied throughout embryonic and postnatal spinal cord development using peptide-specific polyclonal antibodies. As suggested by the 2-D gel analysis and the previously reported expression pattern in cerebral cortex [3], TOAD-64 is transiently expressed in postmitotic spinal cord neurons early in their development and sharply down-regulated after the second postnatal week. In the adult spinal cord, TOAD-64 expression is remarkably restricted to a subset of primary afferents to the spinal cord. This expression pattern, coupled with its recently discovered homology to two proteins implicated in axon pathfinding in the chick and nematode [5,3], suggests that TOAD-64 may have a fundamental role in axon pathfinding.

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Year:  1996        PMID: 8946055     DOI: 10.1016/s0165-3806(96)00132-0

Source DB:  PubMed          Journal:  Brain Res Dev Brain Res        ISSN: 0165-3806


  3 in total

1.  Postnatal alteration of collapsin response mediator protein 4 mRNA expression in the mouse brain.

Authors:  Atsuhiro Tsutiya; Ritsuko Ohtani-Kaneko
Journal:  J Anat       Date:  2012-07-22       Impact factor: 2.610

2.  Phosphorylation of serine 774 of the neural cell adhesion molecule (NCAM) is involved in the interaction with collapsin response mediator protein-2.

Authors:  Yvonne Karbe; Juliane Pollscheit; Nicole Glaubitz; Rüdiger Horstkorte; Kaya Bork
Journal:  Neurochem Res       Date:  2013-02-02       Impact factor: 3.996

Review 3.  Collapsin response mediator proteins (CRMPs): involvement in nervous system development and adult neurodegenerative disorders.

Authors:  Emmanuelle Charrier; Sophie Reibel; Véronique Rogemond; Michèle Aguera; Nicole Thomasset; Jérôme Honnorat
Journal:  Mol Neurobiol       Date:  2003-08       Impact factor: 5.682

  3 in total

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