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Three miRNAs cooperate with host genes involved in human cardiovascular disease

BACKGROUND: Understanding the roles of miRNAs in cardiovascular disease remains a challenge. Genomic linkage indicates a functional relationship between intronic miRNAs and their host genes. However, few studies have shown functional association between intronic miRNAs and their host coding genes th...

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Detalles Bibliográficos
Autores principales: Zhu, Yan, Xie, Jingjing, Sun, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714460/
https://www.ncbi.nlm.nih.gov/pubmed/31464655
http://dx.doi.org/10.1186/s40246-019-0232-4
Descripción
Sumario:BACKGROUND: Understanding the roles of miRNAs in cardiovascular disease remains a challenge. Genomic linkage indicates a functional relationship between intronic miRNAs and their host genes. However, few studies have shown functional association between intronic miRNAs and their host coding genes that are genetically associated with cardiovascular disease. METHODS: In this study, we investigated functional relationship between three protein-coding genes genetically associated with cardiovascular disease, i.e., CDH13, SLC12A3, and CKAP5, and their intronic miRNAs using a data-driven approach. RESULTS: We found that the three protein-coding genes functionally interact with targets of their intronic miRNAs, i.e., miR-3182, miR-6863, and miR-5582, in a tissue-specific pattern. The intronic miRNAs preferentially impact important genes for the three host genes in the network, indicating their roles in maintaining the integrity of the interactome where the host genes are involved. Targets of the intronic miRNAs display functional similarity to the host genes. We furthermore present sets of target genes for future investigation on the possible miRNA-target interactions that potentially contribute to cardiovascular diseases. CONCLUSIONS: Our work provides new insight into the regulatory network of the cardiovascular-associated pathways and opens the possibility for future experimental research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40246-019-0232-4) contains supplementary material, which is available to authorized users.