Proceedings of the National Academy of Sciences · 1994 · 1.1K citations · 19 references
Life SciencesBiochemistryMolecular BiologyMolecular NeuroscienceNeurodegenerationStructural BiologyMolecular Basis Of NeurodegenerationNeurodegeneration MechanismsNeurodegenerative DiseasesNeurodegenerative DisordersProtein StructureSecondary Structure FormationAmino Acid Sequence EffectsAmino Acid Sequence-structure RelationshipsBeta SheetsHydrogen Bonding PatternsPolyglutamine DiseasesPolyglutamine Expansion DisordersStructural Biology Of Neurodegenerative ProteinsX-ray Diffraction Analysis
Four inherited neurodegenerative diseases are linked to abnormally expanded repeats of glutamine residues in the affected proteins. Molecular modeling followed by optical, electron, and x-ray diffraction studies of a synthetic poly(L-glutamine) shows that it forms beta-sheets strongly held together by hydrogen bonds. Glutamine repeats may function as polar zippers, for example, by joining specific transcription factors bound to separate DNA segments. Their extension may cause disease either by increased, nonspecific affinity between such factors or by gradual precipitation of the affected proteins in neurons.
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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
Albert R. La Spada, Elizabeth Wilson, Dennis B. Lubahn et al. · Nature · 1991 · 2.8K citations
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
Harry T. Orr, Ming‐Yi Chung, Sandro Banfi et al. · Nature Genetics · 1993 · 1.7K citations