| Literature DB >> 11860508 |
Klaus Heese1, Takahiro Nakayama, Ryuji Hata, Makoto Masumura, Hiroyasu Akatsu, Feng Li, Yasuo Nagai, Takayuki Yamamoto, Kenji Kosaka, Takahiro Suemoto, Tohru Sawada.
Abstract
The treatment of Alzheimer's disease (AD) remains a major challenge because of the incomplete understanding of the triggering events that lead to the selective neurodegeneration characteristic of AD brains. Here we describe a new protein, CGI-94, that is down-regulated at the mRNA level in the hippocampus of early stage AD brain. Transfection experiments with CGI-94 as a green fluorescent protein (GFP)-fusion-protein show that this protein is translocated into the nucleus of the cell. The finding that this protein, which has a bipartite nuclear localization signal, is also observed in the cytoplasm and extracellular space points to a multifunctional protein. Immunohistochemical analyses reveal that CGI-94 is mainly expressed in neurons of the hippocampal formation and the cortex but not in the cerebellar nucleus. In conclusion, the expression of the nucleolar phosphoprotein CGI-94 appears to be disturbed in early processes of neuronal degeneration.Entities:
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Year: 2002 PMID: 11860508 DOI: 10.1046/j.0953-816x.2001.01836.x
Source DB: PubMed Journal: Eur J Neurosci ISSN: 0953-816X Impact factor: 3.386