Mouse phenogenomics, toolbox for functional annotation of human genome

被引:15
作者
Kim, Il Yong [1 ]
Shin, Jae Hoon [2 ]
Seong, Je Kyung [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Inst Vet Sci, Coll Vet Med, Lab Dev Biol & Genom,Program Vet Sci BK21, Seoul 151742, South Korea
[2] Seoul Natl Univ, Interdisciplinary Program Bioinformat, Seoul 151742, South Korea
[3] Seoul Natl Univ, Program Canc Biol, Seoul 151742, South Korea
关键词
Functional genomics; Genetically engineered mouse; Phenogenomics; Phenotype analysis; RIKEN BIORESOURCE CENTER; MUTAGENESIS PROGRAM; GENE-EXPRESSION; TRANSGENIC MICE; HUMAN-DISEASE; PHENOTYPING RESOURCE; LABORATORY MOUSE; DRUG DEVELOPMENT; MODELS; STRAINS;
D O I
10.5483/BMBRep.2010.43.2.079
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
Mouse models are crucial for the functional annotation of human genome. Gene modification techniques including gene targeting and gene trap in mouse have provided powerful tools in the form of genetically engineered mice (GEM) for understanding the molecular pathogenesis of human diseases. Several international consortium and programs are under way to deliver mutations in every gene in mouse genome. The information from studying these GEM can be shared through international collaboration. However, there are many limitations in utility because not all human genes are knocked out in mouse and they are not yet phenotypically characterized by standardized ways which is required for sharing and evaluating data from GEM. The recent improvement in mouse genetics has now moved the bottleneck in mouse functional genomics from the production of GEM to the systematic mouse phenotype analysis of GEM. Enhanced, reproducible and comprehensive mouse phenotype analysis has thus emerged as a prerequisite for effectively engaging the phenotyping bottleneck. In this review, cur-rent information on systematic mouse phenotype analysis and an issue-oriented perspective will be provided. [BMB reports 2010; 43(2): 79-90]
引用
收藏
页码:79 / 90
页数:12
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