Differential dynamics of the mammalian mRNA and protein expression response to misfolding stress

被引:146
作者
Cheng, Zhe [1 ]
Teo, Guoshou [2 ,3 ]
Krueger, Sabrina [4 ]
Rock, Tara M. [1 ]
Koh, Hiromi W. L. [2 ,3 ]
Choi, Hyungwon [2 ,3 ]
Vogel, Christine [1 ]
机构
[1] NYU, Ctr Genom & Syst Biol, New York, NY USA
[2] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Singapore 117548, Singapore
[3] Natl Univ Hlth Syst, Singapore, Singapore
[4] Max Delbruck Ctr Mol Med, Berlin Inst Med Syst Biol, Berlin, Germany
关键词
Central Dogma; ER stress; mammalian proteomics; mass spectrometry; PECA; ENDOPLASMIC-RETICULUM STRESS; ER-STRESS; LABEL-FREE; CELL-DEATH; TRANSLATION; QUANTIFICATION; SYNTHETASE; SILAC; PHOSPHORYLATION; MITOCHONDRIA;
D O I
10.15252/msb.20156423
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The relative importance of regulation at the mRNA versus protein level is subject to ongoing debate. To address this question in a dynamic system, we mapped proteomic and transcriptomic changes in mammalian cells responding to stress induced by dithiothreitol over 30h. Specifically, we estimated the kinetic parameters for the synthesis and degradation of RNA and proteins, and deconvoluted the response patterns into common and unique to each regulatory level using a new statistical tool. Overall, the two regulatory levels were equally important, but differed in their impact on molecule concentrations. Both mRNA and protein changes peaked between two and eight hours, but mRNA expression fold changes were much smaller than those of the proteins. mRNA concentrations shifted in a transient, pulse-like pattern and returned to values close to pre-treatment levels by the end of the experiment. In contrast, protein concentrations switched only once and established a new steady state, consistent with the dominant role of protein regulation during misfolding stress. Finally, we generated hypotheses on specific regulatory modes for some genes.
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页数:15
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