突变
遗传学
生物
正向遗传学
基因
表型
基因组
基因敲除
基因组编辑
功能(生物学)
基因靶向
反向遗传学
突变体
计算生物学
突变
作者
Abraham Acevedo-Arozena,Sara Wells,Paul K. Potter,M. S. Kelly,Roger D. Cox,Steve Brown
出处
期刊:Annual Review of Genomics and Human Genetics
[Annual Reviews]
日期:2008-09-01
卷期号:9 (1): 49-69
被引量:146
标识
DOI:10.1146/annurev.genom.9.081307.164224
摘要
Arguably, the main challenge for contemporary genetics is to understand the function of every gene in a mammalian genome. The mouse has emerged as a model for this task because its genome can be manipulated in a number of ways to study gene function or mimic disease states. Two complementary genetic approaches can be used to generate mouse models. A reverse genetics or gene-driven approach (gene to phenotype) starts from a known gene and manipulates the genome to create genetically modified mice, such as knockouts. Alternatively, a forward genetics or phenotype-driven approach (phenotype to gene) involves screening mice for mutant phenotypes without previous knowledge of the genetic basis of the mutation. N-ethyl-N-nitrosourea (ENU) mutagenesis has been widely used for both approaches to generate mouse mutants. Here we review progress in ENU mutagenesis screening, with an emphasis on creating mouse models for human disorders.
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