Evolution of the contact phase of vertebrate blood coagulation

被引:106
作者
Ponczek, M. B. [1 ]
Gailani, D. [2 ,3 ]
Doolittle, R. F. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Vanderbilt Univ, Dept Pathol, Nashville, TN USA
[3] Vanderbilt Univ, Dept Med, Nashville, TN USA
关键词
chicken; factor XI; factor XII; opossum; platypus; prekallikrein;
D O I
10.1111/j.1538-7836.2008.03143.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Previous reports have noted that factor (F) XI and FXII and prekallikrein (the contact phase proteases) are absent in fish. Objectives: A broad survey of recently completed genomes was undertaken to find where during the course of vertebrate evolution these coagulation factors appeared. Methods: BLAST searches were conducted for the various factors on genomes of lamprey, puffer fish, zebra fish, frog, chicken, platypus, and opossum. Results: It was confirmed that FXII is absent from fish; it is present in frog, platypus, and opossum, but is absent in chicken, an apparent example of gene loss. A single gene corresponding to the evolutionary predecessor of FXI and prekallikrein occurs in frog, chicken, and platypus. The opossum (a marsupial) has both prekallikrein and FXI, completing the full complement of these genes that occurs in eutherian mammals. Conclusions: The step-by-step accrual of genes for these factors by a series of timely gene duplications has been confirmed by phylogenetic analysis and other considerations.
引用
收藏
页码:1876 / 1883
页数:8
相关论文
共 36 条
[1]  
ALTSHUL SF, 1997, NUCLEIC ACIDS RES, V25, P402
[2]   Lineage-specific loss and divergence of functionally linked genes in eukaryotes [J].
Aravind, L ;
Watanabe, H ;
Lipman, DJ ;
Koonin, EV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (21) :11319-11324
[3]   A new Eocene archaeocete (Mammalia, Cetacea) from India and the time of origin of whales [J].
Bajpai, S ;
Gingerich, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15464-15468
[4]   An overview of ensembl [J].
Birney, E ;
Andrews, TD ;
Bevan, P ;
Caccamo, M ;
Chen, Y ;
Clarke, L ;
Coates, G ;
Cuff, J ;
Curwen, V ;
Cutts, T ;
Down, T ;
Eyras, E ;
Fernandez-Suarez, XM ;
Gane, P ;
Gibbins, B ;
Gilbert, J ;
Hammond, M ;
Hotz, HR ;
Iyer, V ;
Jekosch, K ;
Kahari, A ;
Kasprzyk, A ;
Keefe, D ;
Keenan, S ;
Lehvaslaiho, H ;
McVicker, G ;
Melsopp, C ;
Meidl, P ;
Mongin, E ;
Pettett, R ;
Potter, S ;
Proctor, G ;
Rae, M ;
Searle, S ;
Slater, G ;
Smedley, D ;
Smith, J ;
Spooner, W ;
Stabenau, A ;
Stalker, J ;
Storey, R ;
Ureta-Vidal, A ;
Woodwark, KC ;
Cameron, G ;
Durbin, R ;
Cox, A ;
Hubbard, T ;
Clamp, M .
GENOME RESEARCH, 2004, 14 (05) :925-928
[5]  
BOUMA BN, 1977, J BIOL CHEM, V252, P6432
[6]   Prediction of complete gene structures in human genomic DNA [J].
Burge, C ;
Karlin, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :78-94
[7]   450 million years of hemostasis [J].
Davidson, CJ ;
Tuddenham, EG ;
McVey, JH .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (07) :1487-1494
[8]   Molecular evolution of the vertebrate blood coagulation network [J].
Davidson, CJ ;
Hirt, RP ;
Lal, K ;
Snell, P ;
Elgar, G ;
Tuddenham, EGD ;
McVey, JH .
THROMBOSIS AND HAEMOSTASIS, 2003, 89 (03) :420-428
[9]  
DELEZENNE C, 1897, ARCH PHYSL NORM PATH, V29, P333
[10]  
DIDISHEIM P, 1959, J LAB CLIN MED, V53, P866