Marker-assisted congenic screening (MACS):: A database tool for the efficient production and characterization of congenic lines

被引:18
作者
Collins, SC [1 ]
Wallis, RH [1 ]
Wallace, K [1 ]
Bihoreau, MT [1 ]
Gauguier, D [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
关键词
D O I
10.1007/s00335-002-3058-6
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
Over the past decades, genetic studies in rodent models of human multifactorial disorders have led to the detection of numerous chromosomal regions associated with disease phenotypes. Owing to the complex control of these phenotypes and the size of the disease loci, identifying the underlying genes requires further analyses in new original models, including chromosome substitution (consomic) and congenic lines, derived to evaluate the phenotypic effects of disease susceptibility loci and fine-map the disease genes. We have developed a relational database (MACS) specifically designed for the genetic marker-assisted production of large series of rodent consomic and congenic lines ("speed congenics"), the organization of their genetic and phenotypic characterizations, and the acquisition and archiving of both genetic and phenotypic data. This database, originally optimized for the production of rat congenics, can also be applied to mouse mapping projects. MACS represents an essential system for significantly improving efficiency and accuracy in investigations of multiple consomic and congenic lines simultaneously derived for different disease loci, and ultimately cloning genes underlying complex phenotypes.
引用
收藏
页码:350 / 356
页数:7
相关论文
共 15 条
  • [1] A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps
    Bihoreau, MT
    Sebag-Montefiore, L
    Godfrey, RF
    Wallis, RH
    Brown, JH
    Danoy, PA
    Collins, SC
    Rouard, M
    Kaisaki, PJ
    Lathrop, M
    Gauguier, D
    [J]. GENOMICS, 2001, 75 (1-3) : 57 - 69
  • [2] GRBASE, A NEW GENE-REGULATION DATA-BASE AVAILABLE BY ANONYMOUS FTP
    COLLIER, B
    DANIELSEN, M
    [J]. NUCLEIC ACIDS RESEARCH, 1994, 22 (17) : 3625 - 3625
  • [3] Finding the molecular basis of quantitative traits: Successes and pitfalls
    Flint, J
    Mott, R
    [J]. NATURE REVIEWS GENETICS, 2001, 2 (06) : 437 - 445
  • [4] Gottlieb B, 1999, HUM MUTAT, V14, P103, DOI 10.1002/(SICI)1098-1004(1999)14:2<103::AID-HUMU2>3.3.CO
  • [5] 2-1
  • [6] HOECK WG, 1994, COMPUT APPL BIOSCI, V10, P323
  • [7] Rat genetics: Attaching physiology and pharmacology to the genome
    Jacob, HJ
    Kwitek, AE
    [J]. NATURE REVIEWS GENETICS, 2002, 3 (01) : 33 - 42
  • [8] Applicability of a "speed" congenic strategy to dissect blood pressure quantitative trait loci on rat chromosome 2
    Jeffs, B
    Negrin, CD
    Graham, D
    Clark, JS
    Anderson, NH
    Gauguier, D
    Dominiczak, AF
    [J]. HYPERTENSION, 2000, 35 (01) : 179 - 187
  • [9] Database of mutations that alter the large tumor antigen of simian virus 40
    Kierstead, TD
    Pipas, JM
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (01) : 125 - 126
  • [10] Theoretical and empirical issues for marker-assisted breeding of congenic mouse strains
    Markel, P
    Shu, P
    Ebeling, C
    Carlson, GA
    Nagle, DL
    Smutko, JS
    Moore, KJ
    [J]. NATURE GENETICS, 1997, 17 (03) : 280 - 284