THE EVOLUTIONARY HISTORY OF THE 1ST 3 ENZYMES IN PYRIMIDINE BIOSYNTHESIS

被引:78
作者
DAVIDSON, JN
CHEN, KC
JAMISON, RS
MUSMANNO, LA
KERN, CB
机构
[1] Department of Microbiology and Immunology, University of Kentucky, Lexington, Kentucky
关键词
D O I
10.1002/bies.950150303
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Some metabolic pathways are nearly ubiquitous among organisms: the genes encoding the enzymes for such pathways must therefore be ancient and essential. De novo pyrimidine biosynthesis is an example of one such metabolic pathway. In animals a single protein called CADdagger carries the first three steps of this pathway. The same three enzymes in prokaryotes are associated with separate proteins. The CAD gene appears to have evolved through a process of gene duplication and DNA rearrangement, leading to an in-frame gene fusion encoding a chimeric protein. A driving force for the creation of eukaryotic genes encoding multienzymatic proteins such as CAD may be the advantage of coordinate expression of enzymes catalyzing steps in a biosynthetic pathway. The analogous structure in bacteria is the operon. Differences in the translational mechanisms of eukaryotes and prokaryotes may have dictated the different strategies used by organisms to evolve coordinately regulated genes.
引用
收藏
页码:157 / 164
页数:8
相关论文
共 50 条
[1]   INTRON EXON ORGANIZATION OF THE GENE FOR THE MULTIFUNCTIONAL ANIMAL FATTY-ACID SYNTHASE [J].
AMY, CM ;
WILLIAMSAHLF, B ;
NAGGERT, J ;
SMITH, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (03) :1105-1108
[2]  
BEIN K, 1991, J BIOL CHEM, V266, P3791
[3]   INSITU BEHAVIOR OF THE PYRIMIDINE PATHWAY ENZYMES IN SACCHAROMYCES-CEREVISIAE .2. REACTION-MECHANISM OF ASPARTATE-TRANSCARBAMYLASE DISSOCIATED FROM CARBAMYLPHOSPHATE SYNTHETASE BY GENETIC ALTERATION [J].
BELKAID, M ;
PENVERNE, B ;
DENIS, M ;
HERVE, G .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 254 (02) :568-578
[4]   MAPPING OF CATALYTIC DOMAINS AND PHOSPHORYLATION SITES IN THE MULTIFUNCTIONAL PYRIMIDINE-BIOSYNTHETIC PROTEIN CAD [J].
CARREY, EA ;
HARDIE, DG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 171 (03) :583-588
[5]  
CHRISTOPHERSON RI, 1980, J BIOL CHEM, V255, P1381
[6]  
COLEMAN PF, 1977, J BIOL CHEM, V252, P6379
[7]   USE OF GENE CLONING TO DETERMINE POLARITY OF AN OPERON - GENES CARAB OF ESCHERICHIA-COLI [J].
CRABEEL, M ;
CHARLIER, D ;
WEYENS, G ;
FELLER, A ;
PIERARD, A ;
GLANSDORFF, N .
JOURNAL OF BACTERIOLOGY, 1980, 143 (02) :921-925
[8]   ORGANIZATION AND NUCLEOTIDE-SEQUENCE OF THE 3' END OF THE HUMAN CAD GENE [J].
DAVIDSON, JN ;
RAO, GN ;
NISWANDER, L ;
ANDREANO, C ;
TAMER, C ;
CHEN, KC .
DNA AND CELL BIOLOGY, 1990, 9 (09) :667-676
[9]   PARTIAL CDNA SEQUENCE TO A HAMSTER GENE CORRECTS DEFECT IN ESCHERICHIA-COLI PYRB MUTANT [J].
DAVIDSON, JN ;
NISWANDER, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (22) :6897-6901
[10]  
DAVIDSON JN, 1981, J BIOL CHEM, V256, P5220