Prospects & Overviews
Deciphering the physiological blueprint of a bacterial cell
Revelations of unanticipated complexity in transcriptome and proteome
Article first published online: 18 MAY 2010
Copyright © 2010 WILEY Periodicals, Inc.
Volume 32, Issue 6, pages 461–467, June 2010
How to Cite
Toledo-Arana, A. and Solano, C. (2010), Deciphering the physiological blueprint of a bacterial cell. Bioessays, 32: 461–467. doi: 10.1002/bies.201000020
- Issue published online: 18 MAY 2010
- Article first published online: 18 MAY 2010
- genome-wide transcriptomics;
- tiling arrays
During the last few months, several pioneer genome-wide transcriptomic, proteomic and metabolomic studies have revolutionised the understanding of bacterial biological processes, leading to a picture that resembles eukaryotic complexity. Technological advances such as next-generation high-throughput sequencing and high-density oligonucleotide microarrays have allowed the determination, in several bacteria, of the entire boundaries of all expressed transcripts. Consequently, novel RNA-mediated regulatory mechanisms have been discovered including multifunctional RNAs. Moreover, resolution of bacterial proteome organisation (interactome) and global protein localisation (localizome) have unveiled an unanticipated complexity that highlights the significance of protein multifunctionality and localisation in the cell. Also, analysis of a complete bacterial metabolic network has again revealed a high fraction of multifunctional enzymes and an unexpectedly high level of metabolic responses and adaptation. Altogether, these novel approaches have permitted the deciphering of the entire physiological landscape of one of the smallest bacteria, Mycoplasma pneumoniae. Here, we summarise and discuss recent findings aimed at defining the blueprint of any prokaryote.