Computational Integration of Structural and Functional Genomics Data across Species to Develop Information on the Porcine Inflammatory Gene Regulatory Pathway
Author(s) -
Christopher K. Tuggle,
Y.F. Wang,
Oliver Couture,
LiangHu Qu,
J.J. Uthe,
Daniel Kuhar,
Joan K. Lunney,
Dan Nettleton,
Jack C. M. Dekkers,
Shawn M. D. Bearson
Publication year - 2008
Publication title -
developments in biologicals
Language(s) - English
Resource type - Book series
eISSN - 1662-2960
pISSN - 1424-6074
DOI - 10.1159/000317150
Subject(s) - gene , biology , dna microarray , gene expression profiling , genetics , gene expression , promoter , computational biology , genome , fold change , transcriptome
We are investigating the porcine gut immune response to infection through gene expression profiling. Porcine Affymetrix GeneChip data was obtained from RNA prepared from mesenteric lymph node of swine infected with either Salmonella enterica serovar Typhimurium (ST) or S. Choleraesuis (SC) for 0, 8, 24, 48 or 504 hours post-inoculation (hpi). In total, 2365 genes with statistical evidence for differential expression (DE; p < 0.01, q < 0.26, fold-change > 2) between at least two time-points were identified. Comparative Gene Ontology analyses revealed that a high proportion of annotated DE genes in both infections are involved in immune and defence responses. Hierarchical clustering of expression patterns and annotations showed that 22 of the 83 genes upregulated from 8-24 hpi in the SC infection are known NF-kappaB targets. The promoter sequences of human genes orthologous to the DE genes were collected and TFM-Explorer was used to identify a set of 72 gene promoters with significant over-representation of NF-kappaB DNA-binding motifs. All 22 known NF-kappaB target genes are in this list; we hypothesize that the remaining 51 genes are un-recognized NF-kappaB targets. Integration of these results and verification of putative target genes will increase our understanding of the porcine response pathways responding to bacterial infection.
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