Department of Chemistry and Biotechnology, Graduate School of Engineering, University of Tokyo, Tokyo, Japan.
Department of Applied Life Sciences, School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
Nat Struct Mol Biol. 2017 Sep;24(9):778-782. doi: 10.1038/nsmb.3449. Epub 2017 Aug 7.
The genetic code is not frozen but still evolving, which can result in the acquisition of 'dialectal' codons that deviate from the universal genetic code. RNA modifications in the anticodon region of tRNAs play a critical role in establishing such non-universal genetic codes. In echinoderm mitochondria, the AAA codon specifies asparagine instead of lysine. By analyzing mitochondrial (mt-) tRNA isolated from the sea urchin (Mesocentrotus nudus), we discovered a novel modified nucleoside, hydroxy-N-threonylcarbamoyladenosine (htA), 3' adjacent to the anticodon (position 37). Biochemical analysis revealed that htA37 has the ability to prevent mt-tRNA from misreading AAA as lysine, thereby indicating that hydroxylation of N-threonylcarbamoyladenosine (tA) contributes to the establishment of the non-universal genetic code in echinoderm mitochondria.
遗传密码并非一成不变,仍在不断进化,这可能导致获得偏离通用遗传密码的“方言”密码子。tRNA 反密码子区域的 RNA 修饰在建立这种非通用遗传密码中起着关键作用。在棘皮动物线粒体中,AAA 密码子指定天冬酰胺而不是赖氨酸。通过分析来自海胆(Mesocentrotus nudus)的线粒体 (mt-) tRNA,我们发现了一种新型修饰核苷,羟-N-苏氨酰氨基甲酰腺苷(htA),位于反密码子(位置 37)的 3' 端。生化分析表明,htA37 具有防止 mt-tRNA 将 AAA 错误读为赖氨酸的能力,这表明 N-羟氨基甲酰腺苷(tA)的羟化有助于棘皮动物线粒体中非通用遗传密码的建立。