Unknown

Dataset Information

0

DEAD-box RNA helicase Dbp4/DDX10 is an enhancer of ?-synuclein toxicity and oligomerization.


ABSTRACT: Parkinson's disease is a neurodegenerative disorder associated with misfolding and aggregation of ?-synuclein as a hallmark protein. Two yeast strain collections comprising conditional alleles of essential genes were screened for the ability of each allele to reduce or improve yeast growth upon ?-synuclein expression. The resulting 98 novel modulators of ?-synuclein toxicity clustered in several major categories including transcription, rRNA processing and ribosome biogenesis, RNA metabolism and protein degradation. Furthermore, expression of ?-synuclein caused alterations in pre-rRNA transcript levels in yeast and in human cells. We identified the nucleolar DEAD-box helicase Dbp4 as a prominent modulator of ?-synuclein toxicity. Downregulation of DBP4 rescued cells from ?-synuclein toxicity, whereas overexpression led to a synthetic lethal phenotype. We discovered that ?-synuclein interacts with Dbp4 or its human ortholog DDX10, sequesters the protein outside the nucleolus in yeast and in human cells, and stabilizes a fraction of ?-synuclein oligomeric species. These findings provide a novel link between nucleolar processes and ?-synuclein mediated toxicity with DDX10 emerging as a promising drug target.

SUBMITTER: Popova B 

PROVIDER: S-EPMC7928443 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications


Parkinson's disease is a neurodegenerative disorder associated with misfolding and aggregation of α-synuclein as a hallmark protein. Two yeast strain collections comprising conditional alleles of essential genes were screened for the ability of each allele to reduce or improve yeast growth upon α-synuclein expression. The resulting 98 novel modulators of α-synuclein toxicity clustered in several major categories including transcription, rRNA processing and ribosome biogenesis, RNA metabolism and  ...[more]

Similar Datasets

| S-EPMC2216682 | biostudies-literature
| S-EPMC5733242 | biostudies-literature
| S-EPMC4605566 | biostudies-literature
| S-EPMC4211656 | biostudies-literature
| S-EPMC8775783 | biostudies-literature
| S-EPMC4135551 | biostudies-literature
| S-EPMC27181 | biostudies-literature
| S-EPMC2577925 | biostudies-literature
| S-EPMC3280988 | biostudies-literature
2021-09-08 | PXD028122 | Pride