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

  • Tingting Qin
  • , Nabil Matmati
  • , Lam C. Tsoi
  • , Bidyut K. Mohanty
  • , Nan Gao
  • , Jijun Tang
  • , Andrew B. Lawson
  • , Yusuf A. Hannun
  • , W. Jim Zheng
  • University of Michigan, Ann Arbor
  • Stony Brook University
  • Medical University of South Carolina
  • University of South Carolina
  • Tianjin University
  • University of Texas Health Science Center at Houston

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

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.

Original languageEnglish
Article numbere138
JournalNucleic Acids Research
Volume42
Issue number18
DOIs
StatePublished - Oct 13 2014

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