Liao Guochun, Wang Jianmei, Guo Jingshu, Allard John, Cheng Janet, Ng Anh, Shafer Steve, Puech Anne, McPherson John D, Foernzler Dorothee, Peltz Gary, Usuka Jonathan
Department of Genetics and Genomics, Roche Palo Alto, 3431 Hillview Avenue, Palo Alto, CA 94304-1397, USA.
Science. 2004 Oct 22;306(5696):690-5. doi: 10.1126/science.1100636.
Computational tools can markedly accelerate the rate at which murine genetic models can be analyzed. We developed a computational method for mapping phenotypic traits that vary among inbred strains onto haplotypic blocks. This method correctly predicted the genetic basis for strain-specific differences in several biologically important traits. It was also used to identify an allele-specific functional genomic element regulating H2-Ealpha gene expression. This functional element, which contained the binding sites for YY1 and a second transcription factor that is probably serum response factor, is located within the first intron of the H2-Ealpha gene. This computational method will greatly improve our ability to identify the genetic basis for a variety of phenotypic traits, ranging from qualitative trait information to quantitative gene expression data, which vary among inbred mouse strains.
计算工具能够显著加快对小鼠遗传模型的分析速度。我们开发了一种计算方法,用于将近交系之间存在差异的表型性状映射到单倍型块上。该方法正确预测了几种生物学重要性状中品系特异性差异的遗传基础。它还被用于识别一个调节H2-Ealpha基因表达的等位基因特异性功能基因组元件。这个功能元件包含YY1和另一个可能是血清反应因子的转录因子的结合位点,位于H2-Ealpha基因的第一个内含子内。这种计算方法将极大地提高我们识别各种表型性状遗传基础的能力,这些性状从定性性状信息到定量基因表达数据不等,在近交小鼠品系之间存在差异。