Positive Darwinian selection in Vipera palaestinae phospholipase A2 genes is unexpectedly limited to the third exon

被引:31
作者
Kordis, D [1 ]
Bdolah, A
Gubensek, F
机构
[1] Jozef Stefan Inst, Dept Biochem & Mol Biol, Ljubljana, Slovenia
[2] Tel Aviv Univ, Dept Zool, IL-69978 Tel Aviv, Israel
[3] Univ Ljubljana, Fac Chem & Chem Technol, Dept Chem & Biochem, Ljubljana, Slovenia
关键词
D O I
10.1006/bbrc.1998.9528
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
The venom of Vipera palaestinae contains a two-component toxin, consisting of an acidic phospholipase A(2) (PLA(2)) and a basic protein. Here we report the cloning and sequence analysis of the complete V. palaestinae PLA(2) genes. Since in all Viperidae PLA(2) multigene families the 5' and 3' flanking regions are highly conserved, we designed oligonucleotide primers that allow amplification of the whole PLA(2) multigene family in a single step. The structural organization of both genes is the same as in the Vipera ammodytes PLA(2) multigene family, there being five exons separated by four introns. Comparison of V. palaestinae PLA(2) genes with other Viperidae PLA(2) genes has shown that the structural organization of the genes and the nucleotide sequence of all introns and flanking regions are highly conserved, whereas the third exon clearly shows a higher number of amino acid replacements, an indication of positive Darwinian selection, The positive Darwinian selection is surprisingly limited to the third exon, in contrast to other Viperidae PLA(2) genes, where it is present in all mature protein coding exons. (C) 1998 Academic Press.
引用
收藏
页码:613 / 619
页数:7
相关论文
共 30 条
[1]   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
[2]  
[Anonymous], 1997, VENOM PHOSPHOLIPASE
[3]  
[Anonymous], 1997, Venom phospholipase A2 enzymes: structure, function and mechanism
[4]  
Bon C, 1997, VENOM PHOSPHOLIPASE, P269
[5]  
DENNIS EA, 1994, J BIOL CHEM, V269, P13057
[6]   ACCELERATED EVOLUTION IN THE REACTIVE CENTER REGIONS OF SERINE PROTEASE INHIBITORS [J].
HILL, RE ;
HASTIE, ND .
NATURE, 1987, 326 (6108) :96-99
[7]   PATTERN OF NUCLEOTIDE SUBSTITUTION AT MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I LOCI REVEALS OVERDOMINANT SELECTION [J].
HUGHES, AL ;
NEI, M .
NATURE, 1988, 335 (6186) :167-170
[8]   A phospholipase A(2)-like pseudogene retaining the highly conserved introns of mojave toxin and other snake venom group II PLA(2)s, but having different exons [J].
John, TR ;
Smith, JJ ;
Kaiser, IJ .
DNA AND CELL BIOLOGY, 1996, 15 (08) :661-668
[9]   GENOMIC SEQUENCES ENCODING THE ACIDIC AND BASIC SUBUNITS OF MOJAVE TOXIN - UNUSUALLY HIGH SEQUENCE IDENTITY OF NONCODING REGIONS [J].
JOHN, TR ;
SMITH, LA ;
KAISER, II .
GENE, 1994, 139 (02) :229-234
[10]   A MODEL TO EXPLAIN THE PHARMACOLOGICAL EFFECTS OF SNAKE-VENOM PHOSPHOLIPASES-A2 [J].
KINI, RM ;
EVANS, HJ .
TOXICON, 1989, 27 (06) :613-635