Maddelein M L, Wickner R B
Laboratory of Biochemistry and Genetics, National Institute of Diabetes Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0830, USA.
Mol Cell Biol. 1999 Jun;19(6):4516-24. doi: 10.1128/MCB.19.6.4516.
Ure2p of Saccharomyces cerevisiae normally functions in blocking utilization of a poor nitrogen source when a good nitrogen source is available. The non-Mendelian genetic element [URE3] is a prion (infectious protein) form of Ure2p, so that overexpression of Ure2p induces the de novo appearance of infectious [URE3]. Earlier studies defined a prion domain comprising Ure2p residues 1 to 64 and a nitrogen regulation domain included in residues 66 to 354. We find that deletion of individual runs of asparagine within the prion domain reduce prion-inducing activity. Although residues 1 to 64 are sufficient for prion induction, the fragment from residues 1 to 80 is a more efficient inducer of [URE3]. In-frame deletion of a region around residue 224 does not affect nitrogen regulation but does eliminate prion induction by the remainder of Ure2p. Larger deletions removing the region around residue 224 and more of the C-terminal part of Ure2p restore prion-inducing ability. A fragment of Ure2p lacking the original prion domain does not induce [URE3], but surprisingly, further deletion of residues 151 to 157 and 348 to 354 leaves a fragment that can do so. The region from 66 to 80 and the region around residue 224 are both necessary for this second prion-inducing activity. Thus, each of two nonoverlapping parts of Ure2p is sufficient to induce the appearance of the [URE3] prion.
酿酒酵母的Ure2p通常在有优质氮源时发挥作用,阻止对劣质氮源的利用。非孟德尔遗传元件[URE3]是Ure2p的一种朊病毒(传染性蛋白质)形式,因此Ure2p的过表达会诱导传染性[URE3]的从头出现。早期研究确定了一个包含Ure2p第1至64位残基的朊病毒结构域和一个包含在第66至354位残基中的氮调节结构域。我们发现,在朊病毒结构域内单个天冬酰胺序列的缺失会降低朊病毒诱导活性。虽然第1至64位残基足以诱导朊病毒形成,但第1至80位残基的片段是[URE3]更有效的诱导剂。第224位残基周围区域的框内缺失不影响氮调节,但会消除Ure2p其余部分的朊病毒诱导作用。去除第224位残基周围区域和Ure2p更多C末端部分的更大缺失恢复了朊病毒诱导能力。缺乏原始朊病毒结构域的Ure2p片段不会诱导[URE3],但令人惊讶的是,进一步缺失第151至157位残基和第348至354位残基会留下一个能够诱导[URE3]的片段。第66至80位残基区域和第224位残基周围区域对于这种第二种朊病毒诱导活性都是必需的。因此,Ure2p的两个不重叠部分中的每一个都足以诱导[URE3]朊病毒的出现。