Ammodytoxin C gene helps to elucidate the irregular structure of Crotalinae group II phospholipase A(2) genes

被引:37
作者
Kordis, D
Gubensek, F
机构
[1] Department of Biochemistry and Molecular Biology, Jožef Stefan Institute, 61111 Ljubljana
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1996年 / 240卷 / 01期
关键词
neurotoxic phospholipase A2; gene structure; intron retention; ART-2; retroposon; Vipera ammodytes;
D O I
10.1111/j.1432-1033.1996.0083h.x
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
Ammodytoxin C is a presynaptically neurotoxic phospholipase A(2) (PLA(2)) expressed in the venom glands of Vipera ammodytes (subfamily Viperinae). The gene spans more than 4 kb and consists of five exons and four introns characteristic of group II phospholipase A(2) genes. The first exon encodes the 5' untranslated region, the second exon encodes most of the signal peptide, while exons 3-5 encode three parts of the mature protein. Comparison of the Crotalinae and Viperinae PLA(2) genes has shown that Crotalinae PLA(2) retain the first intron in their mRNAs. The apparent cause of this retention is a deletion of 40 bp in the first exon of PLA(2) genes of the subfamily Crotalinae, which prevents splicing of the first intron. Analysis of the secondary structure of the pre-mRNA of the ammodytoxin C gene has shown that the first exon is able to form an intra-exon hairpin which is absent in Crotalinae PLA(2) pre-mRNAs. Our results indicate that this intra-exon hairpin structure is essential for the splicing of the retained first intron. Contrary to the predictions of the neutral theory of molecular evolution, the introns of all known snake venom PLA(2) genes are conserved up to 90%, that is considerably more than the exons. Consequently it is proposed that highly conserved introns, in multigene families, which evolve under positive Darwinian selection, may have an important role in enabling homologous recombination.
引用
收藏
页码:83 / 90
页数:8
相关论文
共 48 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   PREMESSENGER RNA SECONDARY STRUCTURE AND THE REGULATION OF SPLICING [J].
BALVAY, L ;
LIBRI, D ;
FISZMAN, MY .
BIOESSAYS, 1993, 15 (03) :165-169
[3]   EXON RECOGNITION IN VERTEBRATE SPLICING [J].
BERGET, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (06) :2411-2414
[4]   GENERAL METHOD FOR ISOLATION OF HIGH MOLECULAR-WEIGHT DNA FROM EUKARYOTES [J].
BLIN, N ;
STAFFORD, DW .
NUCLEIC ACIDS RESEARCH, 1976, 3 (09) :2303-2308
[5]   ANALYSIS OF CDNAS ENCODING THE 2 SUBUNITS OF CROTOXIN, A PHOSPHOLIPASE-A2 NEUROTOXIN FROM RATTLESNAKE VENOM - THE ACIDIC NON ENZYMATIC SUBUNIT DERIVES FROM A PHOSPHOLIPASE-A2-LIKE PRECURSOR [J].
BOUCHIER, C ;
BOULAIN, JC ;
BON, C ;
MENEZ, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1088 (03) :401-408
[6]  
COOPER TA, 1992, J BIOL CHEM, V267, P5330
[7]   EVOLUTIONARY RELATIONSHIPS AND IMPLICATIONS FOR THE REGULATION OF PHOSPHOLIPASE-A2 FROM SNAKE-VENOM TO HUMAN SECRETED FORMS [J].
DAVIDSON, FF ;
DENNIS, EA .
JOURNAL OF MOLECULAR EVOLUTION, 1990, 31 (03) :228-238
[8]  
DENNIS EA, 1992, ADV EXP MED BIOL, V318, P35
[9]  
DESILVA AMM, 1995, J MOL EVOL, V41, P174
[10]   STRUCTURE AND EVOLUTIONARY IMPLICATIONS OF A CYSTEINE-RICH CAMPOLETIS-SONORENSIS POLYDNAVIRUS GENE FAMILY [J].
DIBHAJJ, SD ;
WEBB, BA ;
SUMMERS, MD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3765-3769