Paralogs for several proteins implicated in neurodegenerative disorders have been identified and explored to further facilitate the identification of molecular mechanisms contributing to disease pathogenesis. For the disease-causing protein in spinocerebellar ataxia type 2, ataxin-2, a paralog of unknown function, termed ataxin-2-like, has been described. We discovered that ataxin-2-like associates with known interaction partners of ataxin-2, the RNA helicase DDX6 and the poly(A)-binding protein, and with ataxin-2 itself. Furthermore, we found that ataxin-2-like is a component of stress granules. Interestingly, sole ataxin-2-like overexpression led to the induction of stress granules, while a reduction of stress granules was detected in cas...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
International audienceA growing number of human neurodegenerative diseases result from the expansion...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
<div><p>Paralogs for several proteins implicated in neurodegenerative disorders have been identified...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Tight control of translation is fundamental for eukaryotic cells, and deregulation of proteins impli...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative movement disorder ca...
Ataxin-2 is a cytoplasmic protein, product of the ATXN2 gene, whose deficiency leads to obesity, whi...
Ataxin-2 (ATXN2) is a eukaryotic RNA-binding protein that is conserved from yeast to human. Genetic ...
Ataxin-2 is a novel protein, within which the unstable expansion of a polyglutamine domain can cause...
Biomolecular condensation underlies the biogenesis of an expanding array of membraneless assemblies,...
Spinocerebellar ataxia type 2 is an inherited neurodegenerative disorder that is caused by an expand...
RNA-binding proteins play fundamental roles in the regulation of molecular processes critical to cel...
Ataxin-2 (ATXN2) is implicated mainly in mRNA processing. Some ATXN2 associates with receptor tyrosi...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
International audienceA growing number of human neurodegenerative diseases result from the expansion...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
<div><p>Paralogs for several proteins implicated in neurodegenerative disorders have been identified...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Tight control of translation is fundamental for eukaryotic cells, and deregulation of proteins impli...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative movement disorder ca...
Ataxin-2 is a cytoplasmic protein, product of the ATXN2 gene, whose deficiency leads to obesity, whi...
Ataxin-2 (ATXN2) is a eukaryotic RNA-binding protein that is conserved from yeast to human. Genetic ...
Ataxin-2 is a novel protein, within which the unstable expansion of a polyglutamine domain can cause...
Biomolecular condensation underlies the biogenesis of an expanding array of membraneless assemblies,...
Spinocerebellar ataxia type 2 is an inherited neurodegenerative disorder that is caused by an expand...
RNA-binding proteins play fundamental roles in the regulation of molecular processes critical to cel...
Ataxin-2 (ATXN2) is implicated mainly in mRNA processing. Some ATXN2 associates with receptor tyrosi...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
International audienceA growing number of human neurodegenerative diseases result from the expansion...