Prion - Fungi

Fungi

Fungal proteins exhibiting templated conformational change were discovered in the yeast Saccharomyces cerevisiae by Reed Wickner in the early 1990s. For their mechanistic similarity to mammalian prions, they were termed yeast prions. Subsequently, a prion has also been found in the fungus Podospora anserina. These prions behave similarly to PrP, but are generally nontoxic to their hosts. Susan Lindquist's group at the Whitehead Institute has argued some of the fungal prions are not associated with any disease state, but may have a useful role; however, researchers at the NIH have also provided arguments suggesting fungal prions could be considered a diseased state. Thus, the issue of whether fungal proteins are diseases, or have evolved for some specific functions, still remains unresolved.

As of 2012, there are eight known prion proteins in fungi, seven in Saccharomyces cerevisiae (Sup35, Rnq1, Ure2, Swi1, Mot3, Cyc8 and Mod5) and one in Podospora anserina (HET-s). The article that reported the discovery of a prion form the Mca1 protein has recently been retracted due to the fact that the data could not be reproduced. Notably, most of the fungal prions are based on glutamine/asparagine-rich sequences, with the exception of HET-s and Mod5.

Research into fungal prions has given strong support to the protein-only concept, since purified protein extracted from cells with a prion state has been demonstrated to convert the normal form of the protein into a misfolded form in vitro, and in the process, preserve the information corresponding to different strains of the prion state. It has also shed some light on prion domains, which are regions in a protein that promote the conversion into a prion. Fungal prions have helped to suggest mechanisms of conversion that may apply to all prions, though fungal prions appear distinct from infectious mammalian prions in the lack of cofactor required for propagation. The characteristic prion domains may vary between species—e.g. characteristic fungal prion domains are not found in mammalian prions.

Fungal Prions
Protein Natural host Normal function Prion state Prion phenotype Year identified
Ure2p Saccharomyces cerevisiae Nitrogen catabolite repressor Growth on poor nitrogen sources 1994
Sup35p S. cerevisiae Translation termination factor Increased levels of nonsense suppression 1994
HET-S Podospora anserina Regulates heterokaryon incompatibility Heterokaryon formation between incompatible strains
Rnq1p S. cerevisiae Protein template factor , Promotes aggregation of other prions
Mca1 S. cerevisiae Putative yeast caspase Unknown 2008
Swi1 S. cerevisiae Chromatin remodeling Poor growth on some carbon sources 2008
Cyc8 S. cerevisiae Transcriptional repressor Transcriptional derepression of multiple genes 2009
Mot3 S. cerevisiae Nuclear transcription factor Transcriptional derepression of anaerobic genes 2009
Sfp1 S. cerevisiae Putative transcription factor Antisuppression 2010

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