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

被引:62
作者
Chan, Clement T. Y. [1 ]
Deng, Wenjun [1 ]
Li, Fugen [2 ]
DeMott, Michael S. [1 ]
Babu, I. Ramesh [1 ]
Begley, Thomas J. [4 ]
Dedon, Peter C. [1 ,3 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, BioMicro Ctr, Cambridge, MA 02139 USA
[3] MIT, Ctr Environm Hlth Sci, Cambridge, MA 02139 USA
[4] SUNY Albany, Coll Nanoscale Sci, Albany, NY 12203 USA
基金
美国国家科学基金会; 新加坡国家研究基金会;
关键词
BINDING PROTEIN ABP140; BASE EXCISION-REPAIR; ALKYLATING-AGENTS; MASS-SPECTROMETRY; STRESS-RESPONSE; DNA; DATABASE; DAMAGE; METHYLTRANSFERASE; TRANSLATION;
D O I
10.1021/acs.chemrestox.5b00004
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:978 / 988
页数:11
相关论文
共 56 条
[11]   A Quantitative Systems Approach Reveals Dynamic Control of tRNA Modifications during Cellular Stress [J].
Chan, Clement T. Y. ;
Dyavaiah, Madhu ;
DeMott, Michael S. ;
Taghizadeh, Koli ;
Dedon, Peter C. ;
Begley, Thomas J. .
PLOS GENETICS, 2010, 6 (12) :1-9
[12]   THE ESCHERICHIA-COLI ALKB PROTEIN PROTECTS HUMAN-CELLS AGAINST ALKYLATION-INDUCED TOXICITY [J].
CHEN, BRJ ;
CARROLL, P ;
SAMSON, L .
JOURNAL OF BACTERIOLOGY, 1994, 176 (20) :6255-6261
[13]   Toxicogenomics: The challenges and opportunities to identify biomarkers, signatures and thresholds to support mode-of-action [J].
Currie, Richard A. .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2012, 746 (02) :97-103
[14]   MODOMICS: a database of RNA modification pathways. 2008 update [J].
Czerwoniec, Anna ;
Dunin-Horkawicz, Stanislaw ;
Purta, Elzbieta ;
Kaminska, Katarzyna H. ;
Kasprzak, Joanna M. ;
Bujnicki, Janusz M. ;
Grosjean, Henri ;
Rother, Kristian .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D118-D121
[15]   A domain of the actin binding protein Abp140 is the yeast methyltransferase responsible for 3-methylcytidine modification in the tRNA anti-codon loop [J].
D'Silva, Sonia ;
Haider, Steffen J. ;
Phizicky, Eric M. .
RNA, 2011, 17 (06) :1100-1110
[16]   Motifs of serine and threonine can drive association of transmembrane helices [J].
Dawson, JP ;
Weinger, JS ;
Engelman, DM .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 316 (03) :799-805
[17]   Comprehensive mass-spectrometry-based proteome quantification of haploid versus diploid yeast [J].
de Godoy, Lyris M. F. ;
Olsen, Jesper V. ;
Cox, Juergen ;
Nielsen, Michael L. ;
Hubner, Nina C. ;
Froehlich, Florian ;
Walther, Tobias C. ;
Mann, Matthias .
NATURE, 2008, 455 (7217) :1251-U60
[18]   Reactive nitrogen species in the chemical biology of inflammation [J].
Dedon, PC ;
Tannenbaum, SR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2004, 423 (01) :12-22
[19]   A System of RNA Modifications and Biased Codon Use Controls Cellular Stress Response at the Level of Translation [J].
Dedon, Peter C. ;
Begley, Thomas J. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2014, 27 (03) :330-337
[20]   OXIDATIVE DAMAGE TO DNA IN MAMMALIAN CHROMATIN [J].
DIZDAROGLU, M .
MUTATION RESEARCH, 1992, 275 (3-6) :331-342