PQBP-1 (Np/PQ): A polyglutamine tract-binding and nuclear inclusion-forming protein

被引:26
作者
Okazawa, H
Sudol, M
Rich, T
机构
[1] Univ Tokyo, Dept Neurol, Bunkyo Ku, Tokyo 1138655, Japan
[2] Mt Sinai Med Ctr, Dept Med, New York, NY 10029 USA
[3] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
关键词
polyglutamine; WW domains; neuronal cell death; transcription; Huntingtin; splicing; PQBP-1; POU; U5-15kD; dim1;
D O I
10.1016/S0361-9230(01)00579-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Polyglutamine(Q) tract binding protein-1 (PQBP-1) was isolated on the basis of its interaction with polyglutamine tracts and localizes predominantly to the nucleus where it suppresses transcriptional activation by a neuron-specific transcription factor, Brn-2. Its C-terminal domain is highly conserved and binds to a component of the spliceosome. PQBP-1 possesses unique repetitive sequences that may fold as polar zippers. Interestingly, PQBP-1 also forms nuclear inclusion bodies, which are similar to those nucleated by the protein products of polyglutamine disease genes. Furthermore, because PQBP-1 is highly conserved in simple animal metazoans and plants (Caenorhabditis elegans and Arabidopsis), it may perform a basic function in cells. By the same token, disruption of the basic function could be critical to the disease process. Collectively, PQBP-1 might be a candidate molecule involved in the pathology of polyglutamine diseases. In this review, we discuss the structure and function of the PQBP-1 protein, the relevance of its aggregation and possible roles in normal and disease processes. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:273 / 280
页数:8
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