4.5 Article

Highly Predictive Reprogramming of tRNA Modifications Is Linked to Selective Expression of Codon-Biased Genes

Journal

CHEMICAL RESEARCH IN TOXICOLOGY
Volume 28, Issue 5, Pages 978-988

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrestox.5b00004

Keywords

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Funding

  1. National Science Foundation [CHE-1308839]
  2. U.S. National Institute of Environmental Health Science [ES002109, ES017010]
  3. National Cancer Institute [CA026731]
  4. Singapore-MIT Alliance for Research and Technology - National Research Foundation of Singapore

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Cells respond to stress by controlling gene expression at several levels, with little-known about the role of translation. Here, We demonstrate a coordinated translational stress response System involving stress-specific reprogramming of tRNA wobble;modifications that leads to selective translation of codon-biased mRNAs representing different classes of critical. response proteins. In budding yeast exposed to four oxidants and five alkylating agents, tRNA modification. patterns accurately distinguished among chemically similar stressors, with 14 modified ribonucleosides forming the basis for a data driven model that predicts toxicant chemistry with >80% sensitivity and specificity. tRNA Modification subpatterns also distinguish S(N)1 from S(N)2 alkylating agents, with S(N)2-induced increases in m(3)C in tRNA mechanistically linked to selective translation of threonine rich membrane proteins from genes enriched with ACC and ACT degenerate codons for threonine. These results establish tRNA modifications as predictive biomarkers of exposure and illustrate a novel regulatory mechanism for translational control of cell stress response.

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