Role of the cytoplasmic domain of the L1 cell adhesion molecule in brain development

Yukiko Nakamura, Suni Lee, Candace L. Haddox, Eli J. Weaver, Vance P. Lemmon

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Mutations in the human L1CAM gene cause X-linked hydrocephalus and MASA (Mental retardation, Aphasia, Shuffling gait, Adducted thumbs) syndrome. In vitro studies have shown that the L1 cytoplasmic domain (L1CD) is involved in L1 trafficking, neurite branching, signaling, and interactions with the cytoskeleton. L1cam knockout (L1KO) mice have hydrocephalus, a small cerebellum, hyperfasciculation of corticothalamic tracts, and abnormal peripheral nerves. To explore the function of the L1CD, we made three new mice lines in which different parts of the L1CD have been altered. In all mutant lines L1 protein is expressed and transported into the axon. Interestingly, these new L1CD mutant lines display normal brain morphology. However, the expression of L1 protein in the adult is dramatically reduced in the two L1CD mutant lines that lack the ankyrin-binding region and they show defects in motor function. Therefore, the L1CD is not responsible for the major defects observed in L1KO mice, yet it is required for continued L1 protein expression and motor function in the adult.

Original languageEnglish (US)
Pages (from-to)1113-1132
Number of pages20
JournalJournal of Comparative Neurology
Volume518
Issue number7
DOIs
StatePublished - Apr 1 2010

Keywords

  • Axon guidance
  • Fasciculationmyelin
  • Hydrocephalus
  • L1-CAM

ASJC Scopus subject areas

  • Neuroscience(all)

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