http://www.cnr.it/ontology/cnr/individuo/prodotto/ID38617
LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. (Articolo in rivista)
- Type
- Label
- LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Alternative label
C. Nobile, R. Michelucci, S. Andreazza, E. Pasini, S. Tosatto and P. Striano (2009)
LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.
in Human mutation
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- C. Nobile, R. Michelucci, S. Andreazza, E. Pasini, S. Tosatto and P. Striano (literal)
- Pagina inizio
- Pagina fine
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- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- CNR-Institute of Neurosciences, Section of Padua , Padova, Italy;
Department of Neurosciences, Bellaria Hospital, Bologna, Italy;
Department of Biology, University of Padua, Padova, Italy;
Epilepsy Center, Department of Neurological Sciences, Federico II University, Napoli, Italy; Muscular and Neurodegenerative Diseases Unit, Institute \"G. Gaslini,\" University of Genoa, Genova, Italy. (literal)
- Titolo
- LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. (literal)
- Abstract
- Autosomal dominant lateral temporal
epilepsy (ADLTE) or autosomal dominant partial epilepsy
with auditory features (ADPEAF) is an inherited
epileptic syndrome with onset in childhood/adolescence
and benign evolution. The hallmark of the syndrome
consists of typical auditory auras or ictal aphasia in most
affected family members. ADTLE/ADPEAF is associated
in about half of the families with mutations of the
leucine-rich, glioma-inactivated 1 (LGI1) gene. In addition,
de novo LGI1 mutations are found in about 2% of
sporadic cases with idiopathic partial epilepsy with
auditory features, who are clinically similar to the
majority of patients with ADLTE/ADPEAF but have no
family history. Twenty-five LGI1 mutations have been
described in familial and sporadic lateral temporal
epilepsy patients. The mutations are distributed throughout
the gene and are mostly missense mutations
occurring in both the N-terminal leucine rich repeat
(LRR) and C-terminal EPTP (beta propeller) protein
domains. We show a tridimensional model of the LRR
protein region that allows missense mutations of this
region to be divided into two distinct groups: structural
and functional mutations. Frameshift, nonsense and
splice site point mutations have also been reported that
result in protein truncation or internal deletion. The
various types of mutations are associated with a rather
homogeneous phenotype, and no obvious genotype-
phenotype correlation can be identified. Both truncating
and missense mutations appear to prevent secretion
of mutant proteins, suggesting a loss of function effect of
mutations. The function of LGI1 is unclear. Several
molecular mechanisms possibly leading to lateral temporal
epilepsy are illustrated and briefly discussed. (literal)
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