Human Molecular Genetics, Vol 8, 259-266, Copyright © 1999 by Oxford University Press
P Bjorses, M Pelto-Huikko, J Kaukonen, J Aaltonen, L Peltonen and I Ulmanen
Autoimmune-polyendocrinopathy-candidiasis-ecto-dermaldystrophy (APECED) is
the only systemic autoimmune disease with a monogenic background known so
far revealing no association with the major histocompatibility complex
region. We have recently isolated the gene defective in this syndrome and
characterized several different mutations in individuals with the disorder.
The novel gene, AIRE, contains a putative bipartite nuclear targeting
signal predicting a nuclear location of the corresponding protein. The
presence of two PHD-type zinc finger domains as well as the newly described
putative DNA-binding domain, SAND, in the amino acid sequence of the APECED
protein implies that it may be involved in the regulation of gene
expression. Using transient expression of AIRE cDNA in mammalian cells we
demonstrate here the nuclear location of the APECED protein.
Immunohistochemical staining of transfected cells revealed that most of the
recombinant 58 kDa APECED protein is present in the form of nuclear dots.
By double immuno- fluorescence labelling we further show that these
APECED-containing structures and the previously described PML nuclear
bodies are largely non-overlapping. The AIRE protein was also visualized in
multiple human tissues: a subset of the cells in thymus, in spleen and in
lymph node showed nuclear staining with APECED antiserum.
Immunofluorescence labelling of peripheral blood mononuclear leukocytes
also revealed a nuclear body-like staining pattern in a fraction of these
cells. These data from both in vitro and ex vivo systems, together with the
predicted structural features of the APECED protein, suggest that this
protein is most probably involved in the regulation of gene expression.
ARTICLES
Localization of the APECED protein in distinct nuclear structures
Department of Human Molecular Genetics, National Public Health Institute and Department of Medical Genetics, University of Helsinki, Mannerheimintie 166, FIN-00300 Helsinki, Finland.
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