| Literature DB >> 16595690 |
Wei Li1, Louise C Serpell, Wendy J Carter, David C Rubinsztein, James A Huntington.
Abstract
Huntington disease is an inherited neurodegenerative disorder that is caused by expanded CAG trinucleotide repeats, resulting in a polyglutamine stretch of >37 on the N terminus of the protein huntingtin (htt). htt is a large (347 kDa), ubiquitously expressed protein. The precise functions of htt are not clear, but its importance is underscored by the embryonic lethal phenotype in htt knock-out mice. Despite the fact that the htt gene was cloned 13 years ago, little is known about the properties of the full-length protein. Here we report the expression and preliminary characterization of recombinant full-length wild-type human htt. Our results support a model of htt composed entirely of HEAT repeats that stack to form an elongated superhelix.Entities:
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Year: 2006 PMID: 16595690 DOI: 10.1074/jbc.M511007200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157