Transgenic swine for biomedicine and agriculture

被引:156
作者
Prather, RS
Hawley, RJ
Carter, DB
Lai, L
Greenstein, JL
机构
[1] Univ Missouri, Dept Anim Sci, Columbia, MO 65211 USA
[2] Immerge BioTherapeut, Charlestown, MA 02129 USA
[3] Univ Missouri, Dept Vet Pathobiol, Columbia, MO 65211 USA
关键词
transgenic; nuclear transfer; cloning; xenotransplantation;
D O I
10.1016/S0093-691X(02)01263-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Initial technologies for creating transgenic swine only permitted random integration of the construct. However, by combining the technology for homologous recombination in fetal somatic cells with that of nuclear transfer (NT), it is now possible to create specific modifications to the swine genome. The first such example is that of knocking out a gene that is responsible for hyperacute rejection (HAR) when organs from swine are transferred to primates. Because swine are widely used as models of human diseases, there are opportunities for genetic modification to alter these models or to create additional models of human disease. Unfortunately, some of the offspring resulting from NT have abnormal phenotypes. However, it appears that these abnormal phenotypes are a result of epigenetic modifications and, thus, are not transmitted to the offspring of the clones. Although the technique of producing animals with specific genetic modifications by NT has been achieved, improvements to the NT technique as well as improvements in the culture conditions for somatic cells and the techniques for genetic modification are still needed. (C) 2002 Published by Elsevier Science Inc.
引用
收藏
页码:115 / 123
页数:9
相关论文
共 50 条
[1]   In vitro production of embryos in swine [J].
Abeydeera, LR .
THERIOGENOLOGY, 2002, 57 (01) :257-273
[2]   Xenogeneic transplantation [J].
Auchincloss, H ;
Sachs, DH .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :433-470
[3]  
Bleck GT, 1998, J ANIM SCI, V76, P3072
[4]   Cloned pigs generated from cultured skin fibroblasts derived from a H-transferase transgenic boar [J].
Bondioli, K ;
Ramsoondar, J ;
Williams, B ;
Costa, C ;
Fodor, W .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2001, 60 (02) :189-195
[5]   Production of cloned pigs from cultured fetal fibroblast cells [J].
Boquest, AC ;
Grupen, CG ;
Harrison, SJ ;
McIlfatrick, SM ;
Ashman, RJ ;
d'Apice, AJF ;
Nottle, MB .
BIOLOGY OF REPRODUCTION, 2002, 66 (05) :1283-1287
[6]   Transgenic pigs produced using in vitro matured oocytes infected with a retroviral vector [J].
Cabot, RA ;
Kühholzer, B ;
Chan, AWS ;
Lai, L ;
Park, KW ;
Chong, KY ;
Schatten, G ;
Murphy, CN ;
Abeydeera, LR ;
Day, BN ;
Prather, RS .
ANIMAL BIOTECHNOLOGY, 2001, 12 (02) :205-+
[7]  
Carter D. Bart, 2002, Cloning and Stem Cells, V4, P131, DOI 10.1089/153623002320253319
[8]   Engineering passive immunity in transgenic mice secreting virus-neutralizing antibodies in milk [J].
Castilla, J ;
Pintado, B ;
Sola, I ;
Sánchez-Morgado, JM ;
Enjuanes, L .
NATURE BIOTECHNOLOGY, 1998, 16 (04) :349-354
[9]   Transgenic cattle produced by reverse-transcribed gene transfer in oocytes [J].
Chan, AWS ;
Homan, EJ ;
Ballou, LU ;
Burns, JC ;
Bremel, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) :14028-14033
[10]   DEFECTIVE INTRACELLULAR-TRANSPORT AND PROCESSING OF CFTR IS THE MOLECULAR-BASIS OF MOST CYSTIC-FIBROSIS [J].
CHENG, SH ;
GREGORY, RJ ;
MARSHALL, J ;
PAUL, S ;
SOUZA, DW ;
WHITE, GA ;
ORIORDAN, CR ;
SMITH, AE .
CELL, 1990, 63 (04) :827-834