Evolution of the trappin multigene family in the Suidae

被引:23
作者
Furutani, Y
Kato, A
Yasue, H
Alexander, LJ
Beattie, CW
Hirose, S
机构
[1] Tokyo Inst Technol, Dept Biol Sci, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Natl Inst Anim Ind, Anim Genome Res Grp, Tsukuba, Ibaraki 3050902, Japan
[3] US Meat Anim Res Ctr, Clay Ctr, NE 68933 USA
关键词
evolution; exon shuffling; multigene family; protease inhibitor; SINE;
D O I
10.1093/oxfordjournals.jbchem.a022140
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
Trappins are a group of secretory proteins containing a WAP motif with an anchoring domain, Previous studies showed that their genes, especially those of pig, have undergone rapid evolution, which produced trappins with a broad spectrum of actions. To understand the evolution of such a rapidly evolving multigene family, we isolated trappin genes of the Artiodactyla, including pig, wart hog, collared peccary, hippopotamus, and cow, by means of polymerase chain reaction (PCR), Two genes newly isolated from wart hog are orthologs of trappin-1 (SPAI) and trappin-2 (elafin), the others are novel members of the trappin family and named trappins-6 to 11, The divergence of the sequences is greatest in the region that encodes the reactive site, and intron sequences appear to be more highly conserved than the protein-coding sequences, especially among the pig paralogs, Phylogenetic analysis showed that the trappin multigene family members of pig were generated through gene duplication after the divergence of the Suidae (pig and wart hog) and Tayassuidae (collared peccary), Similarities in the gene structure with seminal vesicle clotting proteins (REST) and WAP motif-containing proteins suggest that trappins are naturally occurring fusion proteins created through exon shuffling between ancestral REST and WAP motif-coding genes.
引用
收藏
页码:491 / 502
页数:12
相关论文
共 47 条
[1]   NOVEL PEPTIDE INHIBITOR (SPAI) OF NA+, K+-ATPASE FROM PORCINE INTESTINE [J].
ARAKI, K ;
KUROKI, J ;
ITO, O ;
KUWADA, M ;
TACHIBANA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 164 (01) :496-502
[2]   Secretory leukoprotease inhibitor: Partnering alpha(1)-proteinase inhibitor to combat pulmonary inflammation [J].
Bingle, L ;
Tetley, TD .
THORAX, 1996, 51 (12) :1273-1274
[3]  
CORONEL CE, 1990, J BIOL CHEM, V265, P6854
[4]   PHYLOGENIES FROM MOLECULAR SEQUENCES - INFERENCE AND RELIABILITY [J].
FELSENSTEIN, J .
ANNUAL REVIEW OF GENETICS, 1988, 22 :521-565
[5]  
FRITZ H, 1988, BIOL CHEM H-S, V369, P79
[6]   Cryptic origin of SPAI, a plasma protein with a transglutaminase substrate domain and the WAP motif, revealed by in situ hybridization and immunohistochemistry [J].
Furukawa, M ;
Suzuki, Y ;
Ghoneim, MA ;
Tachibana, S ;
Hirose, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) :29517-29520
[7]   SYSTEMATIC SCREENING OF YEAST ARTIFICIAL-CHROMOSOME LIBRARIES BY USE OF THE POLYMERASE CHAIN-REACTION [J].
GREEN, ED ;
OLSON, MV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (03) :1213-1217
[8]   THE 2.5 A X-RAY CRYSTAL-STRUCTURE OF THE ACID-STABLE PROTEINASE-INHIBITOR FROM HUMAN MUCOUS SECRETIONS ANALYZED IN ITS COMPLEX WITH BOVINE ALPHA-CHYMOTRYPSIN [J].
GRUTTER, MG ;
FENDRICH, G ;
HUBER, R ;
BODE, W .
EMBO JOURNAL, 1988, 7 (02) :345-351
[9]   Exons lost and found - Unusual evolution of a seminal vesicle transglutaminase substrate [J].
Hagstrom, JE ;
Fautsch, MP ;
Perdok, M ;
Vrabel, A ;
Wieben, ED .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (35) :21114-21119
[10]  
HARRIS SE, 1990, J BIOL CHEM, V265, P9896