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A yeast tRNA mutant that causes pseudohyphal growth exhibits reduced rates of CAG codon translation

机译:导致假菌丝生长的酵母tRNA突变体的CAG密码子翻译率降低

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摘要

In Saccharomyces cerevisiae, the SUP70 gene encodes the CAG-decoding tRNAGln CUG. A mutant allele, sup70-65, induces pseudohyphal growth on rich medium, an inappropriate nitrogen starvation response. This mutant tRNA is also a UAG nonsense suppressor via first base wobble. To investigate the basis of the pseudohyphal phenotype, 10 novel sup70 UAG suppressor alleles were identified, defining positions in the tRNAGln CUG anticodon stem that restrict first base wobble. However, none conferred pseudohyphal growth, showing altered CUG anticodon presentation cannot itself induce pseudohyphal growth. Northern blot analysis revealed the sup70-65 tRNAGln CUG is unstable, inefficiently charged, and 80% reduced in its effective concentration. A stochastic model simulation of translation predicted compromised expression of CAG-rich ORFs in the tRNAGln CUG-depleted sup70-65 mutant. This prediction was validated by demonstrating that luciferase expression in the mutant was 60% reduced by introducing multiple tandem CAG (but not CAA) codons into this ORF. In addition, the sup70-65 pseudohyphal phenotype was partly complemented by overexpressing CAA-decoding tRNAGln UUG, an inefficient wobble-decoder of CAG. We thus show that introducing codons decoded by a rare tRNA near the 5′ end of an ORF can reduce eukaryote translational expression, and that the mutant tRNACUG Gln constitutive pseudohyphal differentiation phenotype correlates strongly with reduced CAG decoding efficiency.
机译:在酿酒酵母中,SUP70基因编码CAG编码的tRNAGln CUG。 sup70-65突变等位基因在丰富培养基上诱导假菌丝生长,这是不适当的氮饥饿反应。经由第一碱基摆动,该突变tRNA还是UAG废话抑制物。为了研究假菌丝表型的基础,鉴定了10个新的sup70 UAG抑制等位基因,定义了限制第一碱基摆动的tRNAGln CUG反密码子茎中的位置。但是,没有人赋予假菌丝生长,表明改变的CUG反密码子呈递本身不能诱导假菌丝生长。 Northern印迹分析显示sup70-65 tRNAGln CUG不稳定,充电效率低,其有效浓度降低了80%。翻译的随机模型模拟预测了tRNAGln CUG缺失的sup70-65突变体中富含CAG的ORF的表达受损。通过证明向该ORF中引入多个串联CAG(而不是CAA)密码子,该突变体中的荧光素酶表达降低了60%,从而验证了这一预测。此外,通过过度表达CAA编码tRNAGln UUG(一种低效的CAG摆动解码器)来部分补充sup70-65假菌丝表型。因此,我们表明引入由ORF的5'端附近的稀有tRNA解码的密码子可以减少真核生物的翻译表达,并且突变tRNACUG Gln组成型假菌丝分化表型与降低的CAG解码效率密切相关。

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