TY - JOUR
T1 - Global quantification of mammalian gene expression control
AU - Schwanhüusser, Björn
AU - Busse, Dorothea
AU - Li, Na
AU - Dittmar, Gunnar
AU - Schuchhardt, Johannes
AU - Wolf, Jana
AU - Chen, Wei
AU - Selbach, Matthias
N1 - Funding Information:
Acknowledgements We thank N. Rajewsky and L. Dölken for fruitful discussions and C. Sommer for technical assistance. M.S. and W.C. are supported by the Helmholtz Association, the German Ministry of Education and Research (BMBF) and the Senate of Berlin by funds aimed at establishing the Berlin Institute of Medical Systems Biology (BIMSB) (grant number 315362A). J.W. is supported by the ForSys-programme of the German Ministry of Education and Research (grant number 315289); D.B. by the Helmholtz Alliance on Systems Biology/MSBN; and N.L. by the China Scholarship Council CSC.
PY - 2011/5/19
Y1 - 2011/5/19
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=79956322553&partnerID=8YFLogxK
U2 - 10.1038/nature10098
DO - 10.1038/nature10098
M3 - Article
C2 - 21593866
AN - SCOPUS:79956322553
SN - 0028-0836
VL - 473
SP - 337
EP - 342
JO - Nature
JF - Nature
IS - 7347
ER -