4.5 Article

N6-methyladenosine in mRNA disrupts tRNA selection and translation-elongation dynamics

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NATURE STRUCTURAL & MOLECULAR BIOLOGY
卷 23, 期 2, 页码 110-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.3148

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资金

  1. US National Institutes of Health (NIH) [GM51266, GM099687]
  2. Knut and Alice Wallenberg Foundation (RiboCORE)
  3. Swedish Research Council
  4. Human Frontier Science Program
  5. NIH [GM111858]
  6. Israel Science Foundation (ISF) [1667/12]
  7. Israeli Centers of Excellence (I-CORE) Program (ISF) [41/11, 1796/12]
  8. Ernest and Bonnie Beutler Research Program
  9. Human Frontier Science Program long-term fellowship
  10. Stanford Bio-X fellowship
  11. US Department of Energy, Office of Biological and Environmental Research, NIH
  12. US National Center for Research Resources, Biomedical Technology Program
  13. US National Institute of General Medical Sciences
  14. Kahn Family Foundation

向作者/读者索取更多资源

N-6-methylation of adenosine (forming m(6)A) is the most abundant post-transcriptional modification within the coding region of mRNA, but its role during translation remains unknown. Here, we used bulk kinetic and single-molecule methods to probe the effect of m(6)A in mRNA decoding. Although m(6)A base-pairs with uridine during decoding, as shown by X-ray crystallographic analyses of Thermus thermophilus ribosomal complexes, our measurements in an Escherichia coli translation system revealed that m(6)A modification of mRNA acts as a barrier to tRNA accommodation and translation elongation. The interaction between an m(6)A-modified codon and cognate tRNA echoes the interaction between a near-cognate codon and tRNA, because delay in tRNA accommodation depends on the position and context of m(6)A within codons and on the accuracy level of translation. Overall, our results demonstrate that chemical modification of mRNA can change translational dynamics.

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