Li Wei, Serpell Louise C, Carter Wendy J, Rubinsztein David C, Huntington James A
Department of Haematology, University of Cambridge, Cambridge Institute for Medical Research, Cambridge CB2 2XY, United Kingdom.
J Biol Chem. 2006 Jun 9;281(23):15916-22. doi: 10.1074/jbc.M511007200. Epub 2006 Apr 4.
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.
亨廷顿舞蹈症是一种遗传性神经退行性疾病,由CAG三核苷酸重复序列扩增引起,导致亨廷顿蛋白(htt)N端出现超过37个谷氨酰胺延伸。htt是一种大型(347 kDa)、广泛表达的蛋白质。htt的确切功能尚不清楚,但其重要性在htt基因敲除小鼠的胚胎致死表型中得到了强调。尽管htt基因在13年前就已被克隆,但对全长蛋白质的特性了解甚少。在此,我们报告重组全长野生型人htt的表达及初步表征。我们的结果支持一种完全由HEAT重复序列组成的htt模型,这些重复序列堆叠形成一个细长的超螺旋。