Evolutionary relationships of the carbamoylphosphate synthetase genes

被引:26
作者
vandenHoff, MJB [1 ]
Jonker, A [1 ]
Beintema, JJ [1 ]
Lamers, WH [1 ]
机构
[1] UNIV GRONINGEN, DEPT BIOCHEM, 9747 AG GRONINGEN, NETHERLANDS
关键词
phylogeny; evolution; carbamoylphosphate synthetase; dihydroorotase; aspartate transcarbamoylase; intron; exon; arginine biosynthesis; pyrimidine biosynthesis;
D O I
10.1007/BF00173161
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
Carbamoylphosphate is a common intermediate in the metabolic pathways leading to the biosynthesis of arginine and pyrimidines, The amino acid sequences of all available proteins that catalyze the formation of carbamoylphosphate were retrieved from Genbank and aligned to estimate their mutual phylogenetic relations. In gram-negative bacteria carbamoylphosphate is synthesized by a two-subunit enzyme with glutaminase and carbamoylphosphate synthetase (CPS) activity, respectively. In gram-positive bacteria and lower eukaryotes this two-subunit CPS has become dedicated to arginine biosynthesis, while in higher eukaryotes the two subunits fused and subsequently lost the glutaminase activity, The CPS dedicated to pyrimidine synthesis is part of a multifunctional enzyme (CPS II), encoding in addition dihydroorotase and aspartate transcarbamoylase. Evidence is presented to strengthen the hypothesis that the two ''kinase'' subdomains of all CPS isozymes arose from a duplication of an ancestral gene in the progenote. A further duplication of the entire CPS gene occurred after the divergence of the plants and before the divergence of the fungi from the eukaryotic root, generating the two isoenzymes involved in either the synthesis of arginine or that of pyrimidines. The mutation rate was found to be five- to tenfold higher after the duplication than before, probably reflecting optimization of the enzymes for their newly acquired specialized function, We hypothesize that this duplication arose from a need for metabolic channeling for pyrimidine biosynthesis as it was accompanied by the tagging of the CPS gene with the genes for dihydroorotase and aspartate transcarbamoylase, and as the duplication occurred independently also in gram-positive bacteria. Analysis of the exon-intron organization of the two ''kinase'' subdomains in CPS I and II suggests that ancient exons may have comprised approx. 19 amino acids, in accordance with the prediction of the ''intron-early'' theory.
引用
收藏
页码:813 / 832
页数:20
相关论文
共 82 条
[71]   MAMMALIAN DIHYDROOROTASE - NUCLEOTIDE-SEQUENCE, PEPTIDE SEQUENCES, AND EVOLUTION OF THE DIHYDROOROTASE DOMAIN OF THE MULTIFUNCTIONAL PROTEIN CAD [J].
SIMMER, JP ;
KELLY, RE ;
RINKER, AG ;
ZIMMERMANN, BH ;
SCULLY, JL ;
KIM, H ;
EVANS, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :174-178
[72]   MAMMALIAN ASPARTATE-TRANSCARBAMYLASE (ATCASE) - SEQUENCE OF THE ATCASE DOMAIN AND INTERDOMAIN LINKER IN THE CAD MULTIFUNCTIONAL POLYPEPTIDE AND PROPERTIES OF THE ISOLATED DOMAIN [J].
SIMMER, JP ;
KELLY, RE ;
SCULLY, JL ;
GRAYSON, DR ;
RINKER, AG ;
BERGH, ST ;
EVANS, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4382-4386
[73]  
SMITH EM, 1990, J BIOL CHEM, V265, P10631
[74]   NUCLEOTIDE-SEQUENCE OF THE PYRIMIDINE SPECIFIC CARBAMOYL PHOSPHATE SYNTHETASE, A PART OF THE YEAST MULTIFUNCTIONAL PROTEIN ENCODED BY THE URA2 GENE [J].
SOUCIET, JL ;
POTIER, S ;
HUBERT, JC ;
LACROUTE, F .
MOLECULAR & GENERAL GENETICS, 1987, 207 (2-3) :314-319
[75]   ORGANIZATION OF THE YEAST URA2 GENE - IDENTIFICATION OF A DEFECTIVE DIHYDROOROTASE-LIKE DOMAIN IN THE MULTIFUNCTIONAL CARBAMOYLPHOSPHATE SYNTHETASE-ASPARTATE TRANSCARBAMYLASE COMPLEX [J].
SOUCIET, JL ;
NAGY, M ;
LEGOUAR, M ;
LACROUTE, F ;
POTIER, S .
GENE, 1989, 79 (01) :59-70
[76]   THE USTILAGO-MAYDIS PYR3 GENE - SEQUENCE AND TRANSCRIPTIONAL ANALYSIS [J].
SPANOS, A ;
KANUGA, N ;
HOLDEN, DW ;
BANKS, GR .
GENE, 1992, 117 (01) :73-79
[77]   TESTING THE EXON THEORY OF GENES - THE EVIDENCE FROM PROTEIN-STRUCTURE [J].
STOLTZFUS, A ;
SPENCER, DF ;
ZUKER, M ;
LOGSDON, JM ;
DOOLITTLE, WF .
SCIENCE, 1994, 265 (5169) :202-207
[79]  
TROTTA PP, 1974, J BIOL CHEM, V249, P492
[80]  
VANDENHOFF MJB, 1995, EUR J BIOCHEM, V228, P351