SOMATIC MOSAICISM OF THE CAG REPEAT EXPANSION IN SPINOCEREBELLAR ATAXIA TYPE-3 MACHADO-JOSEPH-DISEASE

Citation
G. Cancel et al., SOMATIC MOSAICISM OF THE CAG REPEAT EXPANSION IN SPINOCEREBELLAR ATAXIA TYPE-3 MACHADO-JOSEPH-DISEASE, Human mutation, 11(1), 1998, pp. 23-27
Citations number
27
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
10597794
Volume
11
Issue
1
Year of publication
1998
Pages
23 - 27
Database
ISI
SICI code
1059-7794(1998)11:1<23:SMOTCR>2.0.ZU;2-X
Abstract
An expanded and unstable CAG repeat in. the coding region of the MJD1 gene is the mutation responsible for spinocerebellar ataxia 3/Machado- Joseph disease. In order to determine whether there was a higher degre e of instability in affected regions, the size of the expanded CAG rep eat was analyzed in different regions of the central nervous system, i n two unrelated SCA3/MJD patients, The degree of somatic mosaicism was quantified and compared to that in a SCA1 patient. Instability of the expanded CAG repeat was observed in peripheral tissues as well as in CNS of the three patients, but there was no correlation between the de gree of mosaicism and the selective vulnerability of CNS structures. A s in the other diseases caused by expanded CAG repeats, a lower degree of mosaicism was found in the cerebellar cortex of both SCA1 and SCA3 /MJD patients, probably reflecting specific properties of this structu re. In SCA3/MJD, the degree of mosaicism seemed to correlate with age at death rather than with the size of the expanded CAG repeat. Finally , somatic instability was more pronounced in SCA1 than in SCA3/MJD pat ients. (C) 1998 Wiley-Liss, Inc.