SFP1‐mediated prion‐dependent lethality is caused by increased Sup35 aggregation and alleviated by Sis1
[PSI+] is the prion form of the translation termination factor Sup35 (eRF3); [PSI+] strains display nonsense suppression. Another prion‐like element, [ISP+], is linked to antisuppression in a specific background. Transcriptional regulator Sfp1 was shown to be responsible for [ISP+] propagation. In t...
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Veröffentlicht in: | Genes to cells : devoted to molecular & cellular mechanisms 2016-12, Vol.21 (12), p.1290-1308 |
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