Title | In silico genetics: identification of a functional element regulating H2-Ealpha gene expression. |
Publication Type | Journal Article |
Year of Publication | 2004 |
Authors | Liao, G, Wang, J, Guo, J, Allard, J, Cheng, J, Ng, A, Shafer, S, Puech, A, McPherson, JD, Foernzler, D, Peltz, G, Usuka, J |
Journal | Science |
Volume | 306 |
Issue | 5696 |
Pagination | 690-5 |
Date Published | 2004 Oct 22 |
ISSN | 1095-9203 |
Keywords | Alleles, Animals, Binding Sites, Computational Biology, Electrophoretic Mobility Shift Assay, Gene Expression Profiling, Gene Expression Regulation, Genes, MHC Class II, Genetic Variation, H-2 Antigens, Haplotypes, Hydrocarbons, Aromatic, Introns, Liver, Lung, Major Histocompatibility Complex, Mice, Mice, Inbred Strains, Oligodeoxyribonucleotides, Oligonucleotide Array Sequence Analysis, Phenotype, Polymorphism, Single Nucleotide, Receptors, Aryl Hydrocarbon, Regulatory Sequences, Nucleic Acid, Serum Response Factor, Transcription Factors |
Abstract | 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.
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DOI | 10.1126/science.1100636 |
Alternate Journal | Science |
PubMed ID | 15499019 |
Grant List | 1 R01 HG02322-01 / HG / NHGRI NIH HHS / United States |