NR AHLY
AU Liu,J.J.; Lindquist,S.L.
TI Oligopeptide-repeat expansions modulate 'protein-only' inheritance in yeast
QU Nature 1999 Aug 5; 400(6744): 573-6
PT journal article
AB The yeast [PSI+] element represents a new type of genetic inheritance, in which changes in phenotype are transmitted by a 'protein only' mechanism reminiscent of the 'protein-only' transmission of mammalian prion diseases. The underlying molecular mechanisms for both are poorly understood and it is not clear how similar they might be. Sup35, the [PSI+] protein determinant, and PrP, the mammalian prion determinant, have different functions, different cellular locations and no sequence similarity; however, each contains five imperfect oligopeptide repeats-PQGGYQQYN in Sup35 and PHGGGWGQ in PrP. Repeat expansions in PrP produce spontaneous prion diseases. Here we show that replacing the wild-type SUP35 gene with a repeat-expansion mutation induces new [PSI+] elements, the first mutation of its type among these newly described elements of inheritance. In vitro, fully denatured repeat-expansion peptides can adopt conformations rich in beta-sheets and form higher-order structures much more rapidly than wild-type peptides. Our results provide insight into the nature of the conformational changes underlying protein-based mechanisms of inheritance and suggest a link between this process and those producing neurodegenerative prion diseases in mammals.
MH Fungal Proteins/chemistry/*genetics; Genes, Fungal; Mutagenesis; Oligopeptides/genetics/*physiology; Plasmids; Prions/chemistry/genetics; Protein Conformation; Repetitive Sequences, Amino Acid/genetics/*physiology; Saccharomyces cerevisiae/*genetics; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S.
AD Howard Hughes Medical Institute, Department of Molecular Genetics and Cell Biology, University of Chicago, Illinois 60637, USA
SP englisch
PO England