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...
International audienceA growing number of human neurodegenerative diseases result from the expansion...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
Ataxin-2 (human gene symbol ATXN2) acts during stress responses, modulating mRNA translation and nut...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Spinocerebellar ataxia type 2 is an inherited neurodegenerative disorder that is caused by an expand...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative movement disorder ca...
Tight control of translation is fundamental for eukaryotic cells, and deregulation of proteins impli...
Spinocerebellar ataxia type 2 (SCA2) is a hereditary neurodegenerative disorder caused by a trinucle...
Ataxin-2 is a novel protein, within which the unstable expansion of a polyglutamine domain can cause...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Ataxin-2 (ATXN2) is a eukaryotic RNA-binding protein that is conserved from yeast to human. Genetic ...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Ataxin-2 (ATXN2) homologs exist in all eukaryotic organisms and may have contributed to their origin...
International audienceA growing number of human neurodegenerative diseases result from the expansion...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
Ataxin-2 (human gene symbol ATXN2) acts during stress responses, modulating mRNA translation and nut...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Paralogs for several proteins implicated in neurodegenerative disorders have been identified and exp...
Spinocerebellar ataxia type 2 is an inherited neurodegenerative disorder that is caused by an expand...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative movement disorder ca...
Tight control of translation is fundamental for eukaryotic cells, and deregulation of proteins impli...
Spinocerebellar ataxia type 2 (SCA2) is a hereditary neurodegenerative disorder caused by a trinucle...
Ataxin-2 is a novel protein, within which the unstable expansion of a polyglutamine domain can cause...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Ataxin-2 (ATXN2) is a eukaryotic RNA-binding protein that is conserved from yeast to human. Genetic ...
Alternative splicing is a fundamental posttranscriptional mechanism for controlling gene expression,...
Ataxin-2 (ATXN2) homologs exist in all eukaryotic organisms and may have contributed to their origin...
International audienceA growing number of human neurodegenerative diseases result from the expansion...
Spinocerebellar Ataxia Type 2 (SCA2) is caused by expansion of a polyglutamine encoding triplet repe...
Ataxin-2 (human gene symbol ATXN2) acts during stress responses, modulating mRNA translation and nut...