Pigs taking wing with transposons and recombinases

被引:28
作者
Clark, Karl J. [1 ,2 ,3 ]
Carlson, Daniel F. [1 ,2 ]
Fahrenkrug, Scott C. [1 ,2 ,3 ]
机构
[1] Univ Minnesota, Dept Anim Sci, St Paul, MN 55108 USA
[2] Univ Minnesota, Arnold & Mabel Beckman Ctr Transposon Res, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Anim Biotechnol Ctr, St Paul, MN 55108 USA
来源
GENOME BIOLOGY | 2007年 / 8卷
关键词
D O I
10.1186/gb-2007-8-S1-S13
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Swine production has been an important part of our lives since the late Mesolithic or early Neolithic periods, and ranks number one in world meat production. Pig production also contributes to high-value-added medical markets in the form of pharmaceuticals, heart valves, and surgical materials. Genetic engineering, including the addition of exogenous genetic material or manipulation of the endogenous genome, holds great promise for changing pig phenotypes for agricultural and medical applications. Although the first transgenic pigs were described in 1985, poor survival of manipulated embryos; inefficiencies in the integration, transmission, and expression of transgenes; and expensive husbandry costs have impeded the widespread application of pig genetic engineering. Sequencing of the pig genome and advances in reproductive technologies have rejuvenated efforts to apply transgenesis to swine. Pigs provide a compelling new resource for the directed production of pharmaceutical proteins and the provision of cells, vascular grafts, and organs for xenotransplantation. Additionally, given remarkable similarities in the physiology and size of people and pigs, swine will increasingly provide large animal models of human disease where rodent models are insufficient. We review the challenges facing pig transgenesis and discuss the utility of transposases and recombinases for enhancing the success and sophistication of pig genetic engineering. 'The paradise of my fancy is one where pigs have wings.' (GK Chesterton).
引用
收藏
页数:16
相关论文
共 201 条
[1]  
Abuin A, 1996, MOL CELL BIOL, V16, P1851
[2]  
Anderson ED, 1996, MOL MAR BIOL BIOTECH, V5, P114
[3]   Protonged expression of a tysosomat enzyme in mouse tiver after Sleeping Beauty transposon-mediated gene detivery:: imptications for non-virat gene therapy of mucopotysaccharidoses [J].
Aronovich, Elena L. ;
Bell, Jason B. ;
Belur, Lalitha R. ;
Gunther, Roland ;
Koniar, Brenda ;
Erickson, David C. C. ;
Schachem, Patricia A. ;
Matise, Ilze ;
McIvor, R. Scott ;
Whitley, Chester B. ;
Hackett, Perry B. .
JOURNAL OF GENE MEDICINE, 2007, 9 (05) :403-415
[4]   Enhancer trapping in zebrafish using the Sleeping Beauty transposon -: art. no. 62 [J].
Balciunas, D ;
Davidson, AE ;
Sivasubbu, S ;
Hermanson, SB ;
Welle, Z ;
Ekker, SC .
BMC GENOMICS, 2004, 5 (1)
[5]   Evidence and consequence of porcine endogenous retrovirus recombination [J].
Bartosch, B ;
Stefanidis, D ;
Myers, R ;
Weiss, R ;
Patience, C ;
Takeuchi, Y .
JOURNAL OF VIROLOGY, 2004, 78 (24) :13880-13890
[6]   Hyperactive transposase mutants of the Sleeping Beauty transposon [J].
Baus, J ;
Liu, L ;
Heggestad, AD ;
Sanz, S ;
Fletcher, BS .
MOLECULAR THERAPY, 2005, 12 (06) :1148-1156
[7]   Gene insertion and long-term expression in lung mediated by the Sleeping Beauty transposon system [J].
Belur, LR ;
Frandsen, JL ;
Dupuy, AJ ;
Ingbar, DH ;
Largaespada, DA ;
Hackett, PB ;
McIvor, RS .
MOLECULAR THERAPY, 2003, 8 (03) :501-507
[8]  
BISHOP JO, 1989, MOL BIOL MED, V6, P283
[9]  
BISHOP JO, 1997, TRANSGENIC ANIMALS G, P219
[10]   Infection of nonhuman primate cells by pig endogenous retrovirus [J].
Blusch, JH ;
Patience, C ;
Takeuchi, Y ;
Templin, C ;
Roos, C ;
Von der Helm, K ;
Steinhoff, G ;
Martin, U .
JOURNAL OF VIROLOGY, 2000, 74 (16) :7687-7690