In silico genetics:: Identification of a functional element regulating H2-Eα gene expression

被引:99
作者
Liao, GC
Wang, JM
Guo, JS
Allard, J
Cheng, J
Ng, A
Shafer, S
Puech, A
McPherson, JD
Foernzler, D
Peltz, G
Usuka, J
机构
[1] Roche Palo Alto, Dept Genet & Genom, Palo Alto, CA 94304 USA
[2] Stanford Univ, Med Ctr, Dept Anesthesia, Stanford, CA 94305 USA
[3] Ctr Natl Genotypage, F-91057 Evry, France
[4] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63108 USA
[5] Washington Univ, Sch Med, Genome Sequencing Ctr, St Louis, MO 63108 USA
[6] Roche Ctr Med Genom F Hoffmann La Roche, CH-4070 Basel, Switzerland
关键词
D O I
10.1126/science.1100636
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:690 / 695
页数:6
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