Department of Cellbiology and Histology, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.
Department of Cellbiology and Histology, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.
J Biol Chem. 2013 Sep 20;288(38):27068-27084. doi: 10.1074/jbc.M113.486076. Epub 2013 Aug 1.
Huntington disease is a neurodegenerative disorder caused by an expanded polyglutamine (polyQ) repeat within the protein huntingtin (Htt). N-terminal fragments of the mutant Htt (mHtt) proteins containing the polyQ repeat are aggregation-prone and form intracellular inclusion bodies. Improving the clearance of mHtt fragments by intracellular degradation pathways is relevant to obviate toxic mHtt species and subsequent neurodegeneration. Because the proteasomal degradation pathway has been the subject of controversy regarding the processing of expanded polyQ repeats, we examined whether the proteasome can efficiently degrade Htt-exon1 with an expanded polyQ stretch both in neuronal cells and in vitro. Upon targeting mHtt-exon1 to the proteasome, rapid and complete clearance of mHtt-exon1 was observed. Proteasomal degradation of mHtt-exon1 was devoid of polyQ peptides as partial cleavage products by incomplete proteolysis, indicating that mammalian proteasomes are capable of efficiently degrading expanded polyQ sequences without an inhibitory effect on the proteasomal activity.
亨廷顿病是一种神经退行性疾病,由蛋白 huntingtin(Htt)内的扩展聚谷氨酰胺(polyQ)重复序列引起。含有 polyQ 重复序列的突变型 Htt(mHtt)蛋白的 N 端片段易于聚集并形成细胞内包涵体。通过细胞内降解途径提高 mHtt 片段的清除率与避免有毒的 mHtt 物种和随后的神经退行性变有关。由于蛋白酶体降解途径在处理扩展的 polyQ 重复序列方面一直存在争议,我们研究了蛋白酶体是否可以在神经元细胞中和体外有效地降解含有扩展 polyQ 延伸的 Htt-exon1。当靶向 mHtt-exon1 到蛋白酶体时,观察到 mHtt-exon1 的快速和完全清除。mHtt-exon1 的蛋白酶体降解没有 polyQ 肽作为不完全蛋白酶解的部分裂解产物,表明哺乳动物蛋白酶体能够有效地降解扩展的 polyQ 序列,而不会对蛋白酶体活性产生抑制作用。