Finding pathway-modulating genes from a novel Ontology Fingerprint-derived gene network

被引:12
|
作者
Qin, Tingting [1 ]
Matmati, Nabil [2 ,3 ]
Tsoi, Lam C. [4 ]
Mohanty, Bidyut K. [5 ]
Gao, Nan [6 ]
Tang, Jijun [6 ,7 ]
Lawson, Andrew B. [8 ]
Hannun, Yusuf A. [2 ,3 ]
Zheng, W. Jim [9 ]
机构
[1] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[2] SUNY Stony Brook, Ctr Canc, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Med, Stony Brook, NY 11794 USA
[4] Univ Michigan, Ctr Stat Genet, Dept Biostat, Ann Arbor, MI 48109 USA
[5] Med Univ S Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[6] Univ S Carolina, Dept Comp Sci & Engn, Columbia, SC 29208 USA
[7] Tianjin Univ, Tianjin Key Lab Cognit Comp & Applicat, Tianjin 300072, Peoples R China
[8] Med Univ S Carolina, Dept Publ Hlth Sci, Charleston, SC 29425 USA
[9] Univ Texas Hlth Sci Ctr Houston, Sch Biomed Informat, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
SACCHAROMYCES-CEREVISIAE GENE; SEMANTIC SIMILARITY; HEAT-STRESS; PROTEINS; YEAST;
D O I
10.1093/nar/gku678
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To enhance our knowledge regarding biological pathway regulation, we took an integrated approach, using the biomedical literature, ontologies, network analyses and experimental investigation to infer novel genes that could modulate biological pathways. We first constructed a novel gene network via a pairwise comparison of all yeast genes' Ontology Fingerprints-a set of Gene Ontology terms overrepresented in the PubMed abstracts linked to a gene along with those terms' corresponding enrichment P-values. The network was further refined using a Bayesian hierarchical model to identify novel genes that could potentially influence the pathway activities. We applied this method to the sphingolipid pathway in yeast and found that many top-ranked genes indeed displayed altered sphingolipid pathway functions, initially measured by their sensitivity to myriocin, an inhibitor of de novo sphingolipid biosynthesis. Further experiments confirmed the modulation of the sphingolipid pathway by one of these genes, PFA4, encoding a palmitoyl transferase. Comparative analysis showed that few of these novel genes could be discovered by other existing methods. Our novel gene network provides a unique and comprehensive resource to study pathway modulations and systems biology in general.
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页数:9
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