ceRNA
ceRNA constructs competing endogenous RNA (ceRNA) networks from paired RNA-seq data to reveal lncRNA–miRNA–mRNA interactions that regulate gene expression.
Key Features:
- ceRNA network construction: Builds ceRNA networks from RNA-seq data by selecting biologically meaningful ceRNA crosstalks.
- Candidate identification: Identifies candidate ceRNA crosstalks based on a competition regulation mechanism between lncRNAs and mRNAs for miRNA binding.
- Competition scoring (PMI): Integrates a competition rule with pointwise mutual information (PMI) to calculate a competition score that quantifies association strength between RNA pairs.
- Significance-based selection: Selects ceRNA crosstalks with significant competition scores to form the final network.
- Biological mechanism: Explicitly models lncRNAs acting as molecular sponges that compete with mRNAs for miRNA binding.
- Total RNA expression consideration: Addresses total RNA expression characteristics when constructing ceRNA interactions from paired RNA-seq data.
Scientific Applications:
- Breast cancer analysis: Applied to paired RNA-seq data to capture regulatory mechanisms relevant to breast cancer.
- Disease mechanism discovery: Reveals ceRNA-mediated regulatory interactions that inform gene regulation in disease contexts.
- Therapeutic target identification: Identifies candidate regulatory axes (lncRNA–miRNA–mRNA) that may suggest potential therapeutic targets.
- General RNA-seq studies: Applicable to other RNA-seq datasets to investigate ceRNA interactions across diseases and biological conditions.
Methodology:
Identify candidate ceRNA crosstalks using a competition regulation mechanism; compute competition scores by integrating a competition rule with pointwise mutual information (PMI); and select crosstalks with significant competition scores to construct the final ceRNA network from paired RNA-seq data.
Topics
Details
- Programming Languages:
- Python
- Added:
- 1/14/2020
- Last Updated:
- 1/9/2021
Operations
Publications
Lan C, Peng H, Hutvagner G, Li J. Construction of competing endogenous RNA networks from paired RNA-seq data sets by pointwise mutual information. BMC Genomics. 2019;20(S9). doi:10.1186/s12864-019-6321-x. PMID:31874629. PMCID:PMC6929403.