Functional genomics and enzyme evolution - Homologous and analogous enzymes encoded in microbial genomes

被引:53
作者
Galperin, MY [1 ]
Koonin, EV [1 ]
机构
[1] Natl Lib Med, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
关键词
D O I
10.1023/A:1003705601428
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Computational analysis of complete genomes, followed by experimental testing of emerging hypotheses - the area of research often referred to as 'functional genomics' - aims at deciphering the wealth of information contained in genome sequences and at using it to improve our understanding of the mechanisms of cell function. This review centers on the recent progress in the genome analysis with special emphasis on the new insights in enzyme evolution. Standard methods of predicting functions for new proteins are listed and the common errors in their application are discussed. A new method of improving the functional predictions is introduced, based on a phylogenetic approach to functional prediction, as implemented in the recently constructed Clusters of Orthologous Groups (COG) database (available at http://www.ncbi.nlm.nih.gov/COG). This approach provides a convenient way to characterize the protein families (and metabolic pathways) that are present or absent in any given organism. Comparative analysis of microbial genomes based on this approach shows that metabolic diversity generally correlates with the genome size-parasitic bacteria code for fewer enzymes and lesser number of metabolic pathways than their free-living relatives. Comparison of different genomes reveals another evolutionary trend, the non-orthologous gene displacement of some enzymes by unrelated proteins with the same cellular function. An examination of the phylogenetic distribution of such cases provides new clues to the problems of biochemical evolution, including evolution of glycolysis and the TCA cycle.
引用
收藏
页码:159 / 170
页数:12
相关论文
共 54 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]  
ALTSCHUL SF, 1997, DNA PROTEIN SEQUENCE, P137
[4]   The PRINTS protein fingerprint database in its fifth year [J].
Attwood, TK ;
Beck, ME ;
Flower, DR ;
Scordis, P ;
Selley, JN .
NUCLEIC ACIDS RESEARCH, 1998, 26 (01) :304-308
[5]   The PROSITE database, its status in 1997 [J].
Bairoch, A ;
Bucher, P ;
Hofmann, K .
NUCLEIC ACIDS RESEARCH, 1997, 25 (01) :217-221
[6]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[7]  
BORK P, 1993, PROTEIN SCI, V2, P31
[8]   Cloning and characterization of the yeast HEM14 gene coding for protoporphyrinogen oxidase, the molecular target of diphenyl ether-type herbicides [J].
Camadro, JM ;
Labbe, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) :9120-9128
[9]   PHYLOGENY AND ONTOGENY OF THE PHOSPHOGLYCERATE MUTASES .4. DISTRIBUTION OF GLYCERATE-2,3-P2 DEPENDENT AND INDEPENDENT PHOSPHOGLYCERATE MUTASES IN ALGAE, FUNGI, PLANTS AND ANIMALS [J].
CARRERAS, J ;
MEZQUITA, J ;
BOSCH, J ;
BARTRONS, R ;
PONS, G .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1982, 71 (04) :591-597
[10]   The crystal structure of a class II fructose-1,6-bisphosphate aldolase shows a novel binuclear metal-binding active site embedded in a familiar fold [J].
Cooper, SJ ;
Leonard, GA ;
McSweeney, SM ;
Thompson, AW ;
Naismith, JH ;
Qamar, S ;
Plater, A ;
Berry, A ;
Hunter, WN .
STRUCTURE, 1996, 4 (11) :1303-1315