Proteome-wide alterations in Escherichia coli translation rates upon anaerobiosis.
Mol Cell Proteomics
; 9(11): 2508-16, 2010 Nov.
Article
em En
| MEDLINE
| ID: mdl-20713451
ABSTRACT
Enzyme reprofiling in bacteria during adaptation from one environmental condition to another may be regulated by both transcription and translation. However, little is known about the contribution of translational regulation. Recently, we have developed a pulse labeling method using the methionine analog azidohomoalanine to determine the relative amounts of proteins synthesized by Escherichia coli in a brief time frame upon a change in environmental conditions. Here we present an extension of our analytical strategy, which entails measuring changes in total protein levels on the same time scale as new protein synthesis. This allows identification of stable and labile proteins and demonstrates that altered levels of most newly synthesized proteins are the result of a change in translation rate rather than degradation rate. With this extended strategy, average relative translation rates for 10 min immediately after a switch from aerobiosis to anaerobiosis were determined. The majority of proteins with increased synthesis rates upon an anaerobic switch are involved in glycolysis and pathways aimed at preventing glycolysis grinding to a halt by a cellular redox imbalance. Our method can be used to compare relative translation rates with relative mRNA levels at the same time. Discrepancies between these parameters may reveal genes whose expression is regulated by translation rather than by transcription. This may help unravel molecular mechanism underlying changes in translation rates, e.g. mediated by small regulatory RNAs.
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Base de dados:
MEDLINE
Assunto principal:
Biossíntese de Proteínas
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Regulação Bacteriana da Expressão Gênica
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Proteoma
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Escherichia coli
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Anaerobiose
Idioma:
En
Ano de publicação:
2010
Tipo de documento:
Article