Too many alanines in ARX (green) result in inclusion bodies.
One alanine repeat–associated disorder, which causes neurological defects in infants, is caused by mutations in the ARX transcription factor. The new results show that 50% expansion of one of ARX's alanine stretches leads to inclusion body formation in neurons. As with glutamine repeat–induced inclusions, the insoluble clumps of mutant ARX are tagged with ubiquitin, as though the cell is trying, yet failing, to degrade the misfolded proteins. Overexpressed Hsp70 chaperone cleared the inclusions.
In cell culture, expression of the mutant ARX increased cell death. Arrasate...
The Rockefeller University Press
2004
The Rockefeller University Press
2004
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