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Hiroki Shibata, Duong P. Huynh, Stefan-M. Pulst, A novel protein with RNA-binding motifs interacts with ataxin-2, Human Molecular Genetics, Volume 9, Issue 9, 22 May 2000, Pages 1303–1313, https://doi.org/10.1093/hmg/9.9.1303
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Abstract
Spinocerebellar ataxia type 2 (SCA2) is caused by expansion of a polyglutamine tract in ataxin-2, a protein of unknown function. Using the yeast two-hybrid system, we identified a novel protein, A2BP1 (ataxin-2 binding protein 1) which binds to the C-terminus of ataxin-2. Northern blot analysis showed that A2BP1 was predominantly expressed in muscle and brain. By immunocfluorescent staining, A2BP1 and ataxin-2 were both localized to the trans-Golgi network. Immunocytochemistry showed that A2BP1 was expressed in the cytoplasm of Purkinje cells and dentate neurons in a pattern similar to that seen for ataxin-2 labeling. Western blot analysis of subcellular fractions indicated enrichment of A2BP1 in the same fractions as ataxin-2. Sequence analysis of the A2BP1 cDNA revealed an RNP motif that is highly conserved among RNA-binding proteins. A2BP1 had striking homology with a human cDNA clone, P83A20, of unknown function and at least two copies of A2BP1 homologs are found in the Caenorhabditis elegans genome database. A2BP1 and related proteins appear to form a novel gene family sharing RNA-binding motifs.
- northern blotting
- western blotting
- yeast one/two-hybrid system
- caenorhabditis elegans
- carrier proteins
- clone cells
- cytoplasm
- dna, complementary
- genes
- genome
- golgi apparatus
- neurons
- purkinje cells
- rna-binding proteins
- sequence analysis
- subcellular fractions
- antibodies
- brain
- rna
- spinocerebellar ataxia type 2
- immunocytochemistry
- polyglutamine
- binding (molecular function)