New proteins involved in spinocerebellar ataxia provide insight into selective neuronal vulnerability
Neurodegenerative disorders like Alzheimer's and Parkinson's disease result from the loss of specific types of neurons due to abnormal accumulation of mutant proteins. Although specific brain regions have been found to be particularly vulnerable in each of these disorders, the causes and exact mechanisms underlying this differential vulnerability of brain cells and regions to toxic mutant proteins are not well understood. A recent study from the lab of Dr. Huda Zoghbi, distinguished service professor at Baylor College of Medicine and founding director of the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital, addressed this question in the context of spinocerebellar ataxia type 1 (SCA 1) and uncovered the diversity of molecular players ...