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CRIM1, a novel gene encoding a cysteine-rich repeat protein, is developmentally regulated and implicated in vertebrate CNS development and organogenesis

Research output: Contribution to journal › Article › peer-review

96 Scopus citations

Abstract

Development of the vertebrate central nervous system is thought to be controlled by intricate cell-cell interactions and spatio-temporally regulated gene expressions. The details of these processes are still not fully understood. We have isolated a novel vertebrate gene, CRIM1/Crim1, in human and mouse. Human CRIM1 maps to chromosome 2p21 close to the Spastic Paraplegia 4 locus. Crim1 is expressed in the notochord, somites, floor plate, early motor neurons and interneuron subpopulations within the developing spinal cord. CRIM1 appears to be evolutionarily conserved and encodes a putative transmembrane protein containing an IGF-binding protein motif and multiple cysteine-rich repeats similar to those in the BMP-associating chordin and sog proteins. Our results suggest a role for CRIM1/Crim1 in CNS development possibly via growth factor binding. Copyright (C) 2000 Elsevier Science Ireland Ltd.

Original languageEnglish
Pages (from-to)181-193
Number of pages13
JournalMechanisms of Development
Volume90
Issue number2
DOIs
StatePublished - 1 Feb 2000
Externally publishedYes

Keywords

  • Bone morphogenic protein
  • Brain
  • C. elegans
  • CNS development
  • Chordin
  • Cysteine-rich repeat
  • Floor plate
  • Hereditary essential tremor 2, Human
  • Holoprosencephaly 2
  • Insulin-like growth factor binding protein
  • Motor neuron
  • Mouse
  • Notochord
  • Organogenesis
  • Short gastrulation
  • Spastic Paraplegia Type 4
  • Spinal cord
  • Transforming growth factor-β

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