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Ataxin-2 Interacts with the DEAD/H-Box RNA Helicase DDX6 and Interferes with P-Bodies and Stress Granules
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Zeitschriftentitel: | Molecular Biology of the Cell |
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Personen und Körperschaften: | , , , , , , , |
In: | Molecular Biology of the Cell, 18, 2007, 4, S. 1385-1396 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
American Society for Cell Biology (ASCB)
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Schlagwörter: |
Zusammenfassung: | <jats:p>Tight control of translation is fundamental for eukaryotic cells, and deregulation of proteins implicated contributes to numerous human diseases. The neurodegenerative disorder spinocerebellar ataxia type 2 is caused by a trinucleotide expansion in the SCA2 gene encoding a lengthened polyglutamine stretch in the gene product ataxin-2, which seems to be implicated in cellular RNA-processing pathways and translational regulation. Here, we substantiate a function of ataxin-2 in such pathways by demonstrating that ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6, a component of P-bodies and stress granules, representing cellular structures of mRNA triage. We discovered that altered ataxin-2 levels interfere with the assembly of stress granules and cellular P-body structures. Moreover, ataxin-2 regulates the intracellular concentration of its interaction partner, the poly(A)-binding protein, another stress granule component and a key factor for translational control. Thus, our data imply that the cellular ataxin-2 concentration is important for the assembly of stress granules and P-bodies, which are main compartments for regulating and controlling mRNA degradation, stability, and translation.</jats:p> |
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Umfang: | 1385-1396 |
ISSN: |
1059-1524
1939-4586 |
DOI: | 10.1091/mbc.e06-12-1120 |