Mind the gap: analysis of marker-assisted breeding strategies for inbred mouse strains

被引:27
作者
Armstrong, NJ [1 ]
Brodnicki, TC
Speed, TP
机构
[1] Netherlands Canc Inst, Div Mol Biol, NL-1066 CX Amsterdam, Netherlands
[2] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[3] Univ Calif Berkeley, Dept Stat, Berkeley, CA 94720 USA
关键词
D O I
10.1007/s00335-005-0123-y
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
The development of congenic mouse strains is the principal approach for confirming and fine mapping quantitative trait loci, as well as for comparing the phenotypic effect of a transgene or gene-targeted disruption between different inbred mouse strains. The traditional breeding scheme calls for at least nine consecutive backcrosses before establishing a congenic mouse strain. Recent availability of genome sequence and high-throughput genotyping now permit the use of polymorphic DNA markers to reduce this number of backcrosses, and empirical data suggest that marker-assisted breeding may require as few as four backcrosses. We used simulation studies to investigate the efficiency of different marker-assisted breeding schemes by examining the trade-off between the number of backcrosses, the number of mice produced per generation, and the number of genotypes per mouse required to achieve a quality congenic mouse strain. An established model of crossover interference was also incorporated into these simulations. The quality of the strain produced was assessed by the probability of an undetected region of heterozygosity (i.e., '' gaps '') in the recipient genetic background, while maintaining the desired donor-derived interval. Somewhat surprisingly, we found that there is a relatively high probability for undetected gaps in potential breeders for establishing a congenic mouse strain. Marker-assisted breeding may decrease the number of backcross generations required to generate a congenic strain, but only additional backcrossing will guarantee a reduction in the number and length of undetected gaps harboring contaminating donor alleles.
引用
收藏
页码:273 / 287
页数:15
相关论文
共 54 条
[1]   Genealogies of mouse inbred strains [J].
Beck, JA ;
Lloyd, S ;
Hafezparast, M ;
Lennon-Pierce, M ;
Eppig, JT ;
Festing, MFW ;
Fisher, EMC .
NATURE GENETICS, 2000, 24 (01) :23-+
[2]  
Bennett B, 1998, MAMM GENOME, V9, P969
[3]   Congenic strains developed for alcohol- and drug-related phenotypes [J].
Bennett, B .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 67 (04) :671-681
[4]   Diabetes protection and restoration of thymocyte apoptosis in NOD Idd6 congenic strains [J].
Bergman, ML ;
Duarte, N ;
Campino, S ;
Lundholm, M ;
Motta, V ;
Lejon, K ;
Penha-Gonçalves, C ;
Holmberg, D .
DIABETES, 2003, 52 (07) :1677-1682
[5]  
BLANK RD, 1988, GENETICS, V120, P1073
[6]   Using mouse models to dissect the genetics of obesity [J].
Brockmann, GA ;
Bevova, MR .
TRENDS IN GENETICS, 2002, 18 (07) :367-376
[7]   A susceptibility allele from a non-diabetes-prone mouse strain accelerates diabetes in NOD congenic mice [J].
Brodnicki, TC ;
Quirk, F ;
Morahan, G .
DIABETES, 2003, 52 (01) :218-222
[8]   Localization of Idd11 using NOD congenic mouse strains:: elimination of Slc9a1 as a candidate gene [J].
Brodnicki, TC ;
McClive, P ;
Couper, S ;
Morahan, G .
IMMUNOGENETICS, 2000, 51 (01) :37-41
[9]  
Broman KW, 2002, GENETICS, V160, P1123
[10]   Mice that are congenic for the char2 locus are susceptible to malaria [J].
Burt, RA ;
Marshall, VM ;
Wagglen, J ;
Rodda, FR ;
Senyschen, D ;
Baldwin, TM ;
Buckingham, LA ;
Foote, SJ .
INFECTION AND IMMUNITY, 2002, 70 (08) :4750-4753