Global quantification of mammalian gene expression control

被引:4754
作者
Schwanhaeusser, Bjoern [1 ]
Busse, Dorothea [1 ]
Li, Na [1 ]
Dittmar, Gunnar [1 ]
Schuchhardt, Johannes [2 ]
Wolf, Jana [1 ]
Chen, Wei [1 ]
Selbach, Matthias [1 ]
机构
[1] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[2] MicroDiscovery GmbH, D-10405 Berlin, Germany
关键词
QUANTITATIVE PROTEOMICS; NUCLEOTIDE RESOLUTION; REGULATORY NETWORKS; IN-VIVO; PROTEIN; DYNAMICS; TRANSLATION; TRANSCRIPTION; STABILITY; CELLS;
D O I
10.1038/nature10098
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene expression is a multistep process that involves the transcription, translation and turnover of messenger RNAs and proteins. Although it is one of the most fundamental processes of life, the entire cascade has never been quantified on a genome-wide scale. Here we simultaneously measured absolute mRNA and protein abundance and turnover by parallel metabolic pulse labelling for more than 5,000 genes in mammalian cells. Whereas mRNA and protein levels correlated better than previously thought, corresponding half-lives showed no correlation. Using a quantitative model we have obtained the first genome-scale prediction of synthesis rates of mRNAs and proteins. We find that the cellular abundance of proteins is predominantly controlled at the level of translation. Genes with similar combinations of mRNA and protein stability shared functional properties, indicating that half-lives evolved under energetic and dynamic constraints. Quantitative information about all stages of gene expression provides a rich resource and helps to provide a greater understanding of the underlying design principles.
引用
收藏
页码:337 / 342
页数:6
相关论文
共 44 条
[11]   Molecular mechanisms of translational control [J].
Gebauer, F ;
Hentze, MW .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (10) :827-835
[12]   Direct multiplexed measurement of gene expression with color-coded probe pairs [J].
Geiss, Gary K. ;
Bumgarner, Roger E. ;
Birditt, Brian ;
Dahl, Timothy ;
Dowidar, Naeem ;
Dunaway, Dwayne L. ;
Fell, H. Perry ;
Ferree, Sean ;
George, Renee D. ;
Grogan, Tammy ;
James, Jeffrey J. ;
Maysuria, Malini ;
Mitton, Jeffrey D. ;
Oliveri, Paola ;
Osborn, Jennifer L. ;
Peng, Tao ;
Ratcliffe, Amber L. ;
Webster, Philippa J. ;
Davidson, Eric H. ;
Hood, Leroy .
NATURE BIOTECHNOLOGY, 2008, 26 (03) :317-325
[13]   Quantitative Proteomics by Metabolic Labeling of Model Organisms [J].
Gouw, Joost W. ;
Krijgsveld, Jeroen ;
Heck, Albert J. R. .
MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (01) :11-24
[14]   The stability of mRNA influences the temporal order of the induction of genes encoding inflammatory molecules [J].
Hao, Shengli ;
Baltimore, David .
NATURE IMMUNOLOGY, 2009, 10 (03) :281-288
[15]   Balancing acts: Molecular control of mammalian iron metabolism [J].
Hentze, MW ;
Muckenthaler, MU ;
Andrews, NC .
CELL, 2004, 117 (03) :285-297
[16]   The ubiquitin system [J].
Hershko, A ;
Ciechanover, A .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :425-479
[17]   Diverse RNA-Binding Proteins Interact with Functionally Related Sets of RNAs, Suggesting an Extensive Regulatory System [J].
Hogan, Daniel J. ;
Riordan, Daniel P. ;
Gerber, Andre P. ;
Herschlag, Daniel ;
Brown, Patrick O. .
PLOS BIOLOGY, 2008, 6 (10) :2297-2313
[18]   Genome-Wide Analysis in Vivo of Translation with Nucleotide Resolution Using Ribosome Profiling [J].
Ingolia, Nicholas T. ;
Ghaemmaghami, Sina ;
Newman, John R. S. ;
Weissman, Jonathan S. .
SCIENCE, 2009, 324 (5924) :218-223
[19]   How proteolysis drives the cell cycle [J].
King, RW ;
Deshaies, RJ ;
Peters, JM ;
Kirschner, MW .
SCIENCE, 1996, 274 (5293) :1652-1659
[20]   Weighing in on ubiquitin: the expanding role of mass-spectrometry-based proteomics [J].
Kirkpatrick, DS ;
Denison, C ;
Gygi, SP .
NATURE CELL BIOLOGY, 2005, 7 (08) :750-757