Publication

Global effects of homocysteine on transcription in escherichia coli: induction of the gene for the major cold-shock protein, cspa

Fraser, K. R.
Citation
Fraser, K. R. (2006). Global effects of homocysteine on transcription in escherichia coli: induction of the gene for the major cold-shock protein, cspa. Microbiology 152 , 2221-2231
Abstract
Homocysteine (Hey) is a thiol-containing amino acid that is considered to be medically important because it is linked to the development of several life-threatening diseases in humans, including cardiovascular disease and stroke. It inhibits the growth of Escherichia coli when supplied in the growth medium. Growth inhibition is believed to arise as a result of partial starvation for isoleucine, which occurs because Hey perturbs the biosynthesis of this amino acid. This study attempted to further elucidate the inhibitory mode of action of Hey by examining the impact of exogenously supplied Hey on the transcriptome. Using gene macroarrays the transcript levels corresponding to 68 genes were found to be reproducibly altered in the presence of 0(.)5 mM Hey. Of these genes, the biggest functional groups affected were those involved in translation (25 genes) and in amino acid metabolism (119 genes). Genes involved in protection against oxidative stress were repressed in Hcy-treated cells and this correlated with a decrease in catalase activity. The gene showing the strongest induction by Hcy was cspA, which encodes the major cold-shock protein CspA. RT-PCR and reporter fusion experiments confirmed that cspA was induced by Hey. Induction of cspA by Hey was not caused by nutritional upshift, a stimulus known to induce C;spA expression, nor was it dependent on the presence of a functional CspA protein. The induction of cspA by Hey was suppressed when isoleucine was included in the growth medium. These data suggest that the induction of CspA expression in the presence of Hcy occurs because of a limitation for isoleucine. The possibility that Hcy-incluced cSPA expression is triggered by translational stalling that occurs when the cells are limited for isoleucine is discussed.
Funder
Publisher
Microbiology Society
Publisher DOI
Rights
Attribution-NonCommercial-NoDerivs 3.0 Ireland