Role of the ribosomal quality control machinery in nucleocytoplasmic translocation of polyQ-expanded huntingtin exon-1

摘要

Abstract The subcellular localization of polyQ-expanded huntingtin exon1 (Httex1) modulates polyQ toxicity in models of Huntington's disease. Using genome-wide screens in a yeast model system, we report that the ribosome quality control (RQC) machinery, recently implicated in neurodegeneration, is a key determinant for the nucleocytoplasmic distribution of Httex1-103Q. Deletion of the RQC genes, LTN1 or RQC1, caused the accumulation of Httex1-103Q in the nucleus through a process that required the CAT-tail tagging activity of Rqc2 and transport via the nuclear pore complex. We provide evidence that nuclear accumulation of Httex1-103Q enhances its cytotoxicity, suggesting that the RQC machinery plays an important role in protecting cells against the adverse effects of polyQ expansion proteins. Highlights ? RQC system interferes with nucleocytoplasmic translocation of Httex1-103Q. ? Deletion of LTN1 causes nuclear accumulation of Httex1-103Q significantly. ? CAT-tailing activity of Rqc2 is required for nuclear accumulation of Httex1-103Q. ? Btn2 is involved in nucleocytoplasmic transport of Httex1-103Q. ? Nuclear accumulation of Httex1-103Q enhances its cytotoxicity.