The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins.

Abstract:

:Recently mutations in the LGI1 (leucine-rich, glioma-inactivated 1) gene have been found in human temporal lobe epilepsy. We have now identified three formerly unknown LGI-like genes. Hydropathy plots and pattern analysis showed that LGI genes encode proteins with large extra- and intracellular domains connected by a single transmembrane region. Sequence analysis demonstrated that LGI1, LGI2, LGI3, and LGI4 form a distinct subfamily when compared to other leucine-rich repeat-containing proteins. In silico mapping and radiation hybrid experiments assigned LGI2, LGI3, and LGI4 to different chromosomal regions (4p15.2, 8p21.3, 19q13.11), some of which have been implicated in epileptogenesis and/or tumorigenesis.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Gu W,Wevers A,Schröder H,Grzeschik KH,Derst C,Brodtkorb E,de Vos R,Steinlein OK

doi

10.1016/s0014-5793(02)02713-8

keywords:

subject

Has Abstract

pub_date

2002-05-22 00:00:00

pages

71-6

issue

1-3

eissn

0014-5793

issn

1873-3468

pii

S0014579302027138

journal_volume

519

pub_type

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