Alternative use of a mini exon of the L1 gene affects L1 binding to neuralligands

Citation
E. De Angelis et al., Alternative use of a mini exon of the L1 gene affects L1 binding to neuralligands, J BIOL CHEM, 276(35), 2001, pp. 32738-32742
Citations number
23
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
276
Issue
35
Year of publication
2001
Pages
32738 - 32742
Database
ISI
SICI code
0021-9258(20010831)276:35<32738:AUOAME>2.0.ZU;2-8
Abstract
Neural cell adhesion molecule Ll is a cell surface glycoprotein required fo r the correct development of the nervous system. Ll exists as two isoforms encoded by mRNA species that either collectively incorporate or exclude exo ns 2 and 27. Neurons utilize only the full-length isoform, whereas Schwann cells, kidney cells, and blood lymphocytes only express the short form of L 1. Still other cells, oligodendrocytes, regulate Ll isoform expression in a maturation-dependent manner. The RSLE motif encoded by exon 27 is known to have a role in clathrin-mediated endocytosis of L1, but the function of th e exon 2-encoded motif (YEGHHV) is unknown. Here we show that this motif is required for the optimal binding of Ll to several neural ligands and is li kely to be important for nervous system development. Thus, alternative use of exon 2 is a mechanism for regulating ligand interactions with L1.