Proteome Organization in a Genome-Reduced Bacterium

Sebastian Kühner(European Molecular Biology Laboratory), Vera van Noort(European Molecular Biology Laboratory), Matthew J. Betts(European Molecular Biology Laboratory), Alejandra Leo‐Macías(European Molecular Biology Laboratory), Claire Batisse(European Molecular Biology Laboratory), Michaela Rode(European Molecular Biology Laboratory), Takuji Yamada(European Molecular Biology Laboratory), Tobias Maier(Universitat Pompeu Fabra), Samuel L. Bader(European Molecular Biology Laboratory), Pedro Beltrán-Álvarez(European Molecular Biology Laboratory), Daniel Castaño‐Díez(European Molecular Biology Laboratory), Wei‐Hua Chen(European Molecular Biology Laboratory), Damien P. Devos(European Molecular Biology Laboratory), Marc Güell(Universitat Pompeu Fabra), Tomás Norambuena(Pontificia Universidad Católica de Chile), Ines Racke(European Molecular Biology Laboratory), Vladimir Rybin(European Molecular Biology Laboratory), Alexander Schmidt(ZHAW Zurich University of Applied Sciences), Eva Yus(Universitat Pompeu Fabra), Ruedi Aebersold(ZHAW Zurich University of Applied Sciences), Richard Herrmann(Heidelberg University), Bettina Böttcher(European Molecular Biology Laboratory), Achilleas S. Frangakis(European Molecular Biology Laboratory), Robert B. Russell(European Molecular Biology Laboratory), Luís Serrano(Institució Catalana de Recerca i Estudis Avançats), Peer Bork(European Molecular Biology Laboratory), Anne‐Claude Gavin(European Molecular Biology Laboratory)
Science
November 27, 2009
Cited by 471

Abstract

Simply Mycoplasma The bacterium Mycoplasma pneumoniae , a human pathogen, has a genome of reduced size and is one of the simplest organisms that can reproduce outside of host cells. As such, it represents an excellent model organism in which to attempt a systems-level understanding of its biological organization. Now three papers provide a comprehensive and quantitative analysis of the proteome, the metabolic network, and the transcriptome of M. pneumoniae (see the Perspective by Ochman and Raghavan ). Anticipating what might be possible in the future for more complex organisms, Kühner et al. (p. 1235 ) combine analysis of protein interactions by mass spectrometry with extensive structural information on M. pneumoniae proteins to reveal how proteins work together as molecular machines and map their organization within the cell by electron tomography. The manageable genome size of M. pneumoniae allowed Yus et al. (p. 1263 ) to map the metabolic network of the organism manually and validate it experimentally. Analysis of the network aided development of a minimal medium in which the bacterium could be cultured. Finally, G‡ell et al. (p. 1268 ) applied state-of-the-art sequencing techniques to reveal that this “simple” organism makes extensive use of noncoding RNAs and has exon- and intron-like structure within transcriptional operons that allows complex gene regulation resembling that of eukaryotes.


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