Strain-dependent differences in the efficiency of transgenic mouse production

被引:67
作者
Auerbach, AB
Norinsky, R
Ho, WL
Losos, K
Guo, QX
Chatterjee, S
Joyner, AL
机构
[1] NYU, Sch Med, Skirball Inst Biomol Med, Dev Genet Program, New York, NY 10016 USA
[2] NYU, Sch Med, Howard Hughes Med Inst, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
[4] NYU, Stern Sch Business, Management Educ Ctr, New York, NY 10012 USA
关键词
egg donor; mouse genetic backgrounds; mouse strains; pronuclear microinjection; transgenesis; transgenic mouse production;
D O I
10.1023/A:1022166921766
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transgenic mouse production via pronuclear microinjection is a complex process consisting of a number of sequential steps. Many different factors contribute to the effectiveness of each step and thus influence the overall efficiency of transgenic mouse production. The response of egg donor females to superovulation, the fertilization rate, egg survival after injection, ability of manipulated embryos to implant and develop to term, and concentration and purity of the injected DNA all contribute to transgenic production efficiency. We evaluated and compared the efficiency of transgenic mouse production using four different egg donor mouse strains: B6D2/F1 hybrids, Swiss Webster (SW) outbred, and inbred FVB/N and C57BL/6. The data included experiments involving similar to350 DNA transgene constructs performed by a high capacity core transgenic mouse facility. Significant influences of particular genetic backgrounds on the efficiency of different steps of the production process were found. Except for egg production, FVB/N mice consistently produced the highest efficiency of transgenic mouse production at each step of the process. B6D2/F2 hybrid eggs are also quite efficient, but lyze more frequently than FVB/N eggs after DNA microinjection. SW eggs on the other hand block at the 1-cell stage more often than eggs from the other strains. Finally, using C57BL/6 eggs the main limiting factor is that the fetuses derived from injected eggs do not develop to term as often as the other strains. Based on our studies, the procedure for transgenic mouse production can be modified for each egg donor strain in order to overcome any deficiencies, and thus to increase the overall efficiency of transgenic mouse production.
引用
收藏
页码:59 / 69
页数:11
相关论文
共 22 条
[1]   LOCALIZATION OF A RETROVIRAL ELEMENT WITHIN THE RD GENE CODING FOR THE BETA-SUBUNIT OF CGMP PHOSPHODIESTERASE [J].
BOWES, C ;
LI, TS ;
FRANKEL, WN ;
DANCIGER, M ;
COFFIN, JM ;
APPLEBURY, ML ;
FARBER, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2955-2959
[2]   FACTORS AFFECTING THE EFFICIENCY OF INTRODUCING FOREIGN DNA INTO MICE BY MICROINJECTING EGGS [J].
BRINSTER, RL ;
CHEN, HY ;
TRUMBAUER, ME ;
YAGLE, MK ;
PALMITER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (13) :4438-4442
[3]   GENE-TRANSFER EFFICIENCY DURING GESTATION AND THE INFLUENCE OF CO-TRANSFER OF NON-MANIPULATED EMBRYOS ON PRODUCTION OF TRANSGENIC MICE [J].
CANSECO, RS ;
SPARKS, AET ;
PAGE, RL ;
RUSSELL, CG ;
JOHNSON, JL ;
VELANDER, WH ;
PEARSON, RE ;
DROHAN, WN ;
GWAZDAUSKAS, FC .
TRANSGENIC RESEARCH, 1994, 3 (01) :20-25
[4]  
Croy BA, 2000, CAN VET J, V41, P201
[5]   DEVELOPMENT OF MOUSE EMBRYOS INVITRO IS AFFECTED BY STRAIN AND CULTURE-MEDIUM [J].
DANDEKAR, PV ;
GLASS, RH .
GAMETE RESEARCH, 1987, 17 (04) :279-285
[6]   A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation (Pdebrd1) in FVB/N-derived transgenic mice [J].
Giménez, E ;
Montoliu, L .
LABORATORY ANIMALS, 2001, 35 (02) :153-156
[7]  
HAMMES A, 2000, PRACT APPROACH SER, V217, P217
[8]  
Hogan B., 1986, MANIPULATING MOUSE E
[9]   AGE-RELATED CNS DISORDER AND EARLY DEATH IN TRANSGENIC FVB/N MICE OVEREXPRESSING ALZHEIMER AMYLOID PRECURSOR PROTEINS [J].
HSIAO, KK ;
BORCHELT, DR ;
OLSON, K ;
JOHANNSDOTTIR, R ;
KITT, C ;
YUNIS, W ;
XU, S ;
ECKMAN, C ;
YOUNKIN, S ;
PRICE, D ;
IADECOLA, C ;
CLARK, HB ;
CARLSON, G .
NEURON, 1995, 15 (05) :1203-1218
[10]  
MANN JR, 1993, METHOD ENZYMOL, V225, P771