Submitted on August 5, 2009
Revised on October 15, 2009
Accepted on October 29, 2009
Proteomic-based refinement of Deinococcus deserti genome annotation reveals an unwonted use of non-canonical translation initiation codons
Mathieu Baudet, Philippe Ortet, Jean-Charles Gaillard, Bernard Fernandez, Philippe Guérin, Christine Enjalbal, Gilles Subra, Arjan de Groot, Mohamed Barakat, Alain Dedieu, and Jean Armengaud
Institute of environmental biology and biotechnology, CEA Marcoule, BAGNOLS-SUR-CEZE F-30207
Corresponding Author: jean.armengaud{at}cea.fr
Deinococcaceae are a family of extremely radiation tolerant bacteria that are currently subjected to numerous studies aimed at understanding the molecular mechanisms for such radiotolerance. To achieve a comprehensive and accurate annotation of the Deinococcus deserti genome, we performed an N-terminal-oriented characterization of its proteome. For this, we used a labeling reagent, N-Tris(2,4,6-trimethoxyphenyl)phosphonium acetyl succinimide (TMPP), to selectively derivatize protein N-termini. The large scale identification of TMPP-modified N-terminal-most peptides by shotgun liquid chromatography-tandem mass spectrometry analysis led to the validation of 278 and the correction of 73 translation initiation codons in D. deserti genome. In addition, four new genes were detected, three located on the main chromosome and one on plasmid P3. We also analyzed signal peptide cleavages on a genome-wide scale. Based on comparative proteogenomic analysis, we propose a set of 137 corrections to improve Deinococcus radiodurans and Deinococcus geothermalis gene annotations. Some of these corrections affect important genes involved in DNA repair mechanisms such as polA, ligA, and ddrB. Surprisingly, experimental evidences were obtained indicating that DnaA (the protein involved in the DNA replication initiation process) and RpsL (the S12 ribosomal conserved protein) translation is initiated in Deinococcaceae from non-canonical codons (ATC and CTG, respectively). Such use may be the basis of specific regulation mechanisms affecting replication and translation. We also report the use of non-conventional translation initiation codons for two other genes: Deide_03051 and infC. Whether such use of non-canonical translation initiation codons is much more frequent than for other previously reported bacterial phyla or restricted to Deinococcaceae remains to be investigated. Our results demonstrate that predicting translation initiation codons is still difficult for some bacteria and that proteomic-based refinement of genome annotations may be helpful in such cases.