B. Tycko et al., POLYMORPHISMS IN THE HUMAN APOLIPOPROTEIN-J CLUSTERIN GENE - ETHNIC VARIATION AND DISTRIBUTION IN ALZHEIMERS-DISEASE/, Human genetics, 98(4), 1996, pp. 430-436
Apolipoprotein-J/clusterin (APOJ/CLI) shares many biological propertie
s with apolipoprotein-E (APOE) including, but not limited to, avid bin
ding with P-amyloid peptide. Thus, APOJ/CLI warrants scrutiny as a can
didate Alzheimer's disease (AD) susceptibility gene. We identified sev
en nucleotide sequence polymorphisms in APOJ/ CLI, two of which, in ex
on 7, alter the predicted amino acid sequence. The JVIIB variant is an
asparagine-to-histidine substitution, which deletes a glycosylation s
ignal at amino acid 317; the JVIIC variant is an aspartate-to-asparagi
ne substitution, which forms a new glycosylation signal at position 32
8. Both of these coding variants, as well as two neutral polymorphisms
in exon 2, were more frequent in African-Americans than Hispanics and
were rare in Caucasians. However; no individual coding or non-coding
variant was consistently associated with AD. At the population level,
APOJ/CLI polymorphisms are frequent among persons of African descent,
but probably do not alter susceptibility to AD.