Phosphoglucose isomerases of hagfish, zebrafish, gray mullet, toad, and snake, with reference to the evolution of the genes in vertebrates

被引:17
作者
Kao, HW [1 ]
Lee, SC [1 ]
机构
[1] Acad Sinica, Inst Zool, Taipei 115, Taiwan
关键词
gene duplication; nonsynonymous substitution; purifying selection; radical amino acid change; synonymous substitution;
D O I
10.1093/oxfordjournals.molbev.a004092
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
Phosphoglucose isomerase (PGI) is a protein with multiple functions. To infer its structure changes and evolution in vertebrates, we cloned cDNAs encoding PGI genes from hagfish (Paramyxine yangi), gray mullet (Mugil cephalus), zebrafish (Danio rerio), toad (Bufo melanosticus), and snake (Boiga kraepelini). Only one PGI gene was cloned in each of hagfish, toad, and snake, but two PGI genes were found in zebrafish and gray mullet, respectively. The PGI of hagfish encodes 554 amino acids, in contrast to the PGIs of bonyfishes, toad, and snake which encode 553 amino acids and the PGIs of mammals which encode 558 amino acids. Among 558 aligned amino acid sites, there are 314 sites (56.27%) totally conserved. To see if diversifying selection acts on PGI amino acids of vertebrates, we calculated the pairwise ratio of nonsynonymous versus synonymous substitution per site (Ka/Ks) and the ratio of radical amino acid chances versus conservative amino acid changes per sites (dR/dC between PGI sequences. The average pairwise ratio between nonsynonymous substitutions per nucleotide (Ka) and synonymous substitutions per nucleotide (Ks) among vertebrate PGI sequences equals 0.047 +/- 0.019. The average pairwise ratio between radical amino acid changes and conservative amino acid changes (dR/dC) among the vertebrate PGIs equal 0.938 +/- 0.158 for charge changes, 0.558 +/- 0.085 for polarity changes, and 0.465 +/- 0.0714 when both polarity and volume are considered. There is no amino acid within the vertebrate PGIs under diversifying selection as analyzed by the method of Yang et al. (2000b). The results suggest that the present vertebrate PGIs are at evolutionary stasis and are being subjected to intense purifying selection. The purifying selection is to maintain polarity and volume of the protein but not the charge groups of amino acids. Phylogenetic analysis reveals that vertebrate PGIs can be classified into three major groups: the mammalian, amphibian-reptilian, and teleostean PGIs. The gene tree suggests that the gene duplication event of PGI in bonyfishes occurred before diversification of Acanthopterygii, but after the split of bonyfishes and tetrapods. The evolution of multiple functions of PGI is discussed.
引用
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页码:367 / 374
页数:8
相关论文
共 40 条
[1]  
[Anonymous], 1991, The Causes of Molecular Evolution
[2]   The PROSITE database, its status in 1995 [J].
Bairoch, A ;
Bucher, P ;
Hofmann, K .
NUCLEIC ACIDS RESEARCH, 1996, 24 (01) :189-196
[3]   Purification of a novel serine proteinase inhibitor from the skeletal muscle of white croaker (Argyrosomus argentatus) [J].
Cao, MJ ;
Osatomi, K ;
Matsuda, R ;
Ohkubo, M ;
Hara, K ;
Ishihara, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 272 (02) :485-489
[4]   THE NEUROTROPHIC FACTOR NEUROLEUKIN IS 90-PERCENT HOMOLOGOUS WITH PHOSPHOHEXOSE ISOMERASE [J].
CHAPUT, M ;
CLAES, V ;
PORTETELLE, D ;
CLUDTS, I ;
CRAVADOR, A ;
BURNY, A ;
GRAS, H ;
TARTAR, A .
NATURE, 1988, 332 (6163) :454-455
[5]   The crystal structure of phosphoglucose isomerase/autocrine motility factor/neuroleukin complexed with its carbohydrate phosphate inhibitors suggests its substrate/receptor recognition [J].
Chou, CC ;
Sun, YJ ;
Meng, MS ;
Hsiao, CD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (30) :23154-23160
[6]   DUPLICATION OF THE GLUCOSEPHOSPHATE ISOMERASE LOCUS IN VERTEBRATES [J].
DANDO, PR .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1980, 66 (03) :373-378
[7]  
*DNASTAR, 1994, LAS
[8]   MOUSE GLUCOSE-6-PHOSPHATE ISOMERASE AND NEUROLEUKIN HAVE IDENTICAL 3' SEQUENCES [J].
FAIK, P ;
WALKER, JIH ;
REDMILL, AAM ;
MORGAN, MJ .
NATURE, 1988, 332 (6163) :455-456
[9]  
FELSENSTEIN J, 1993, PHYLIP PHYL INF PACK
[10]  
FISHER SE, 1980, GENETICA, V52-3, P73