A perfect genome annotation is within reach with the proteomics and genomics alliance

被引:74
作者
Armengaud, Jean [1 ]
机构
[1] CEA, DSV, IBEB, Lab Biochim Syst Perturb, F-30207 Bagnols Sur Ceze, France
关键词
N-TERMINAL PEPTIDES; TANDEM MASS-SPECTRA; SHEWANELLA-ONEIDENSIS MR-1; LARGE-SCALE IDENTIFICATION; POSTTRANSLATIONAL MODIFICATIONS; MYCOBACTERIUM-SMEGMATIS; HALOBACTERIUM-SALINARUM; NATRONOMONAS-PHARAONIS; HYPOTHETICAL PROTEINS; POSITIONAL PROTEOMICS;
D O I
10.1016/j.mib.2009.03.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
High-throughput identification of proteins and their accurate partial sequencing by shotgun nanoLC-MS/MS are now feasible for any cellular model at a full genomic scale. Proteogenomics is the integration of these data with the genome. Mining microbial proteomes allows validation of predicted orphan genes and correction of genome annotation errors such as discovery of unannotated genes, reversal of reading frames and identification of translational start sites, stop codon read-throughs or programmed frameshifts. Recent advances have been achieved in database searches, N-terminal oriented proteomics and homology-driven proteogenomics. From now on, proteogenomics on newly sequenced model genomes can be carried out at the earliest stage of the genome project as already exemplified by Mycoplasma mobile and Deinococcus deserti genomes. The proteomics and genomics alliance produces almost complete and accurate gene catalogues for small microbial genomes, a comprehensiveness which is essential for efficient systems biology.
引用
收藏
页码:292 / 300
页数:9
相关论文
共 62 条
[31]   Localization, annotation, and comparison of the Escherichia coli K-12 proteome under two states of growth [J].
Lopez-Campistrous, A ;
Semchuk, P ;
Burke, L ;
Palmer-Stone, T ;
Brokx, SJ ;
Broderick, G ;
Bottorff, D ;
Bolch, S ;
Weiner, JH ;
Ellison, MJ .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (08) :1205-1209
[32]   From the genome sequence to the proteome and back:: Evaluation of E-coli genome annotation with a 2-D gel-based proteomics approach [J].
Maillet, Isabelle ;
Berndt, Peter ;
Malo, Celine ;
Rodriguez, Sabrina ;
Brunisholz, Rene A. ;
Pragai, Zoltan ;
Arnold, Sabine ;
Langen, Hanno ;
Wyss, Markus .
PROTEOMICS, 2007, 7 (07) :1097-1106
[33]   Positional proteomics: selective recovery and analysis of N-terminal proteolytic peptides [J].
McDonald, L ;
Robertson, DHL ;
Hurst, JL ;
Beynon, RJ .
NATURE METHODS, 2005, 2 (12) :955-957
[34]   Positional proteomics: preparation of amino-terminal peptides as a strategy for proteome simplification and characterization [J].
McDonald, Lucy ;
Beynon, Robert J. .
NATURE PROTOCOLS, 2006, 1 (04) :1790-1798
[35]   Tools for analyzing and predicting N-terminal protein modifications [J].
Meinnel, Thierry ;
Giglione, Carmela .
PROTEOMICS, 2008, 8 (04) :626-649
[36]   Terminal proteomics: N- and C-terminal analyses for high-fidelity identification of proteins using MS [J].
Nakazawa, Takashi ;
Yamaguchi, Minoru ;
Okamura, Taka-aki ;
Ando, Eiji ;
Nishimura, Osamu ;
Tsunasawa, Susumu .
PROTEOMICS, 2008, 8 (04) :673-685
[37]   Parallel identification of new genes in Saccharomyces cerevisiae [J].
Oshiro, G ;
Wodicka, LM ;
Washburn, MP ;
Yates, JR ;
Lockhart, DJ ;
Winzeler, EA .
GENOME RESEARCH, 2002, 12 (08) :1210-1220
[38]   Diversity of translation start sites may define increased complexity of the human short ORFeome [J].
Oyama, Masaaki ;
Kozuka-Hata, Hiroko ;
Suzuki, Yutaka ;
Semba, Kentaro ;
Yamamoto, Tadashi ;
Sugano, Sumio .
MOLECULAR & CELLULAR PROTEOMICS, 2007, 6 (06) :1000-1006
[39]   Towards multidimensional genome annotation [J].
Reed, JL ;
Famili, I ;
Thiele, I ;
Palsson, BO .
NATURE REVIEWS GENETICS, 2006, 7 (02) :130-141
[40]   Genome and proteome annotation: organization, interpretation and integration [J].
Reeves, Gabrielle A. ;
Talavera, David ;
Thornton, Janet M. .
JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2009, 6 (31) :129-147