Aligning ontologies and integrating textual evidence for pathway analysis of microarray data

Gopalan, Banu ; Posse, Christian ; Sanfilippo, Antonio P. ; Stenzel-Poore, Mary ; Stevens, S.L. ; Castano, Jose ; Beagley, Nathaniel ; Riensche, Roderick M. ; Baddeley, Bob ; Simon, R.P. ; Pustejovsky, James

Pacific Northwest National Laboratory (U.S.)

关键词: Gopubmed;    Gene Ontology;    Genes;    Biology;    Pathways;   

DOI  :  10.2172/948766
RP-ID  :  PNNL-16211
RP-ID  :  AC05-76RL01830
RP-ID  :  948766

美国|英语

来源: UNT Digital Library

【 摘 要 】

Expression arrays are introducing a paradigmatic change in biology by shifting experimental approaches from single gene studies to genome-level analysis, monitoring the ex-pression levels of several thousands of genes in parallel. The massive amounts of data obtained from the microarray data needs to be integrated and interpreted to infer biological meaning within the context of information-rich pathways. In this paper, we present a methodology that integrates textual information with annotations from cross-referenced ontolo-gies to map genes to pathways in a semi-automated way. We illustrate this approach and compare it favorably to other tools by analyzing the gene expression changes underlying the biological phenomena related to stroke. Stroke is the third leading cause of death and a major disabler in the United States. Through years of study, researchers have amassed a significant knowledge base about stroke, and this knowledge, coupled with new technologies, is providing a wealth of new scientific opportunities. The potential for neu-roprotective stroke therapy is enormous. However, the roles of neurogenesis, angiogenesis, and other proliferative re-sponses in the recovery process following ischemia and the molecular mechanisms that lead to these processes still need to be uncovered. Improved annotation of genomic and pro-teomic data, including annotation of pathways in which genes and proteins are involved, is required to facilitate their interpretation and clinical application. While our approach is not aimed at replacing existing curated pathway databases, it reveals multiple hidden relationships that are not evident with the way these databases analyze functional groupings of genes from the Gene Ontology.