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Modification of orthogonal tRNAs: unexpected consequences for sense codon reassignment

机译:正交TRNA的修改:感测密码子重新分配的意外后果

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Breaking the degeneracy of the genetic code via sense codon reassignment has emerged as a way to incorporate multiple copies of multiple non-canonical amino acids into a protein of interest. Here, we report the modification of a normally orthogonal tRNA by a host enzyme and show that this adventitious modification has a direct impact on the activity of the orthogonal tRNA in translation. We observed nearly equal decoding of both histidine codons, CAU and CAC, by an engineered orthogonal M. jannaschii tRNA with an AUG anticodon: tRNA(Opt). We suspected a modification of the tRNA(Opt) (AUG) anticodon was responsible for the anomalous lack of codon discrimination and demonstrate that adenosine 34 of tRNA(Opt) (AUG) is converted to inosine. We identified tRNA(Opt) (AUG) anticodon loop variants that increase reassignment of the histidine CAU codon, decrease incorporation in response to the histidine CAC codon, and improve cell health and growth profiles. Recognizing tRNA modification as both a potential pitfall and avenue of directed alteration will be important as the field of genetic code engineering continues to infiltrate the genetic codes of diverse organisms.
机译:通过感测密码子重新分配破坏遗传密码的退化是一种方法作为将多个非典型氨基酸的多个拷贝掺入感兴趣的蛋白质。在这里,我们通过宿主酶报告通常正交的TRNA的修饰,并表明这种偶然修饰对翻译中的正交TRNA的活性直接影响。我们观察到与Aug Antecon:TRNA(OPT)的工程正交的正交M.Jannaschii TRNA对组氨酸密码子,CAU和CAC的几乎相同的解码。我们怀疑TRNA的修饰(OPT)(APE)反致抗体负责缺乏密码子歧视,并证明TRNA(OPT)(AUG)的腺苷34转化为肌苷。我们鉴定了TRNA(OPT)(AUG)抗oryon回路变体,其增加组氨酸CAU密码子的重新分配,响应于组氨酸CAC密码子而减少掺入,并改善细胞健康和生长型材。识别TRNA修改作为导向改变的潜在缺陷和途径将是重要的,因为遗传码工程领域继续渗透不同生物的遗传码。

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