Cargando…
Integrated Analysis of miRNA-mRNA Interaction in Pediatric Dilated Cardiomyopathy
BACKGROUND: microRNAs (miRNAs) are short single stranded nucleotides that can regulate gene expression. Although we previously evaluated expression of miRNAs in pediatric dilated cardiomyopathy (DCM) by miRNA array, pathway prediction based on changes in mRNA expression has not been previous analyze...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602449/ https://www.ncbi.nlm.nih.gov/pubmed/34012027 http://dx.doi.org/10.1038/s41390-021-01548-w |
Sumario: | BACKGROUND: microRNAs (miRNAs) are short single stranded nucleotides that can regulate gene expression. Although we previously evaluated expression of miRNAs in pediatric dilated cardiomyopathy (DCM) by miRNA array, pathway prediction based on changes in mRNA expression has not been previous analyzed in this population. The current study aimed to determine regulation of miRNA expression by miRNA-Seq and, through mRNA-Seq, analyze their putative target genes and altered pathways in pediatric DCM hearts. METHODS: miRNA expression was determined by miRNA-Seq [n=10 non-failing (NF), n=20 DCM]. Expression of a subset of miRNAs was evaluated in adult DCM patients (n=11 NF, n=13 DCM). miRNA-mRNA prediction analysis was performed using mRNA-Seq data (n=7 NF, n=7 DCM) from matched samples. RESULTS: Expression of 393 miRNAs was significantly different (p<0.05) in pediatric DCM patients compared to NF controls. TargetScan-based miRNA-mRNA analysis revealed 808 significantly inversely expressed genes. Functional analysis suggests up-regulated pathways related regulation of stem cell differentiation and cardiac muscle contraction, and down-regulated pathways related to regulation of protein phosphorylation, signal transduction and cell communication. CONCLUSION: Our results demonstrated a unique age-dependent regulation of miRNAs and their putative target genes which may contribute to distinctive phenotypic characteristics of DCM in children. |
---|