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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Hermes Transposon Mutagenesis Shows [URE3] Prion Pathology Prevented by a Ubiquitin-Targeting Protein: Evidence for Carbon/Nitrogen Assimilation Cross Talk and a Second Function for Ure2p in Saccharomyces cerevisiae
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Hermes Transposon Mutagenesis Shows [URE3] Prion Pathology Prevented by a Ubiquitin-Targeting Protein: Evidence for Carbon/Nitrogen Assimilation Cross Talk and a Second Function for Ure2p in Saccharomyces cerevisiae

机译:Hermes转座子诱变显示泛素靶向蛋白质预防的[Ure3]朊病毒病理学:碳/氮同化串扰的证据和酿酒酵母酿酒酵母中的ure2p的第二个功能

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[URE3] is an amyloid-based prion of Ure2p, a regulator of nitrogen catabolism. While most "variants" of the [URE3] prion are toxic, mild variants that only slightly slow growth are more widely studied. The existence of several antiprion systems suggests that some components may be protecting cells from potential detrimental effects of mild [URE3] variants. Our extensive Hermes transposon mutagenesis showed that disruption of YLR352W dramatically slows the growth of [URE3-1] strains. Ylr352wp is an F-box protein, directing selection of substrates for ubiquitination by a "cullin"-containing E-3 ligase. For efficient ubiquitylation, cullin-dependent E-3 ubiquitin ligases must be NEDDylated, modified by a ubiquitin-related peptide called NEDD8 (Rub1p in yeast). Indeed, we find that disruption of NEDDylation-related genes RUB1, ULA1, UBA3, and UBC12 is also counterselected in our screen. We find that like ylr352w [URE3] strains, ylr352w ure2 strains do not grow on nonfermentable carbon sources. Overexpression of Hap4p, a transcription factor stimulating expression of mitochondrial proteins, or mutation of GLN1, encoding glutamine synthetase, allows growth of ylr352w [URE3] strains on glycerol media. Supplying proline as a nitrogen source shuts off the nitrogen catabolite repression (NCR) function of Ure2p, but does not slow growth of ylr352w strains, suggesting a distinct function of Ure2p in carbon catabolism. Also, gln1 mutations impair NCR, but actually relieve the growth defect of ylr352w [URE3] and ylr352w ure2 strains, again showing that loss of NCR is not producing the growth defect and suggesting that Ure2p has another function. YLR352W largely protects cells from the deleterious effects of otherwise mild [URE3] variants or of a ure2 mutation (the latter a rarer event), and we name it LUG1 (lets [URE3]/ure2 grow).
机译:[Ure3]是尿蛋白基朊病毒朊病毒,氮素分解代谢的调节剂。虽然[Ure3]朊病毒的大多数“变体”是有毒的,但只有略微缓慢的增长,更加缓慢地研究了轻度变异。几种止前体系的存在表明,一些组分可以保护细胞免受轻度[Ure3]变体的潜在不利影响。我们广泛的Hermes转座子诱变表明,YLR352W的破坏显着减缓了[Ure3-1]菌株的生长。 YLR352WP是一种F箱蛋白,通过“CULLIN” - 甲基连接酶指示ubiquitination的基材选择。为了有效的ubiquitylation,Cullin依赖性E-3泛素连接酶必须用众所可在蛋白相关的肽改性,被称为NEDD8(酵母中的RUB1P)。实际上,我们发现在我们的屏幕中也会发现与Neddylation相关基因rub1,Ula1,UbA3和UBC12的破坏。我们发现,如ylr352w [ure3]菌株,Ylr352w ure2菌株不会在非活动碳源上生长。 HAP4P的过度表达,刺激线粒体蛋白的表达,或GLN1的突变,编码谷氨酰胺合成酶,允许在甘油介质上生长YLR352W [URE3]菌株。作为氮源供应脯氨酸,关闭URE2P的氮抗粘土抑制(NCR)功能,但不缓解YLR352W菌株的增长,表明URE2P在碳分解代谢中的不同功能。此外,GLN1突变损害NCR,但实际上缓解YLR352W [URE3]和YLR352W URE2菌株的生长缺陷,再次表明NCR的丧失不会产生生长缺陷并表明URE2P具有另一种功能。 YLR352W主要保护细胞免受其他温和[URE3]变体或URE2突变(后一种RARER事件)的有害影响的细胞,并且我们将其命名为LUG1(让[URE3] / Ure2生长)。

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