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MicroRNA Expression Profiles of Human iPS Cells, Retinal Pigment Epithelium Derived From iPS, and Fetal Retinal Pigment Epithelium
Published on: June 24, 2014
Identification of differentially expressed microRNAs across the developing human brain
11] National Institute of Child Health and Human Development, NIH, Bethesda, MD, USA [2] NIH-University of Cambridge Biomedical Scholars Program, Cambridge, UK [3] Baylor College of Medicine MSTP, Houston, TX, USA.
Molecular Psychiatry
|August 7, 2013
Summary
This study maps microRNA (miRNA) expression in the developing human brain. Key miRNAs were linked to neurodevelopmental disorders like autism and schizophrenia.
Area of Science:
- Neuroscience
- Genetics
- Developmental Biology
Background:
- MicroRNAs (miRNAs) are crucial regulators of gene expression.
- Understanding miRNA dynamics during human brain development is vital for insights into neurodevelopmental disorders.
Purpose of the Study:
- To perform a spatio-temporal analysis of miRNA expression in the developing human brain.
- To identify miRNAs and their target genes involved in early brain development and sex-specific patterns.
- To investigate the association of miRNA targets with neurodevelopmental and psychiatric disorders.
Main Methods:
- RNA sequencing (RNA-seq) was used to analyze miRNA expression.
- The study included 18 human donor brains from infancy to adolescence, focusing on the prefrontal cortex, hippocampus, and cerebellum.
- Bioinformatic analyses identified differentially expressed miRNAs, their target genes, and functional enrichments.
Main Results:
- Significant spatio-temporal patterns and sex differences in miRNA expression were observed in the prefrontal cortex.
- Identified miRNA targets were enriched for functions in transcription regulation and synaptogenesis.
- miRNA targets showed strong enrichment for gene sets associated with autism, schizophrenia, bipolar disorder, and depression.
Conclusions:
- The study highlights the critical role of specific miRNAs in the transcriptional networks of the developing human brain.
- These findings suggest that dysregulated miRNAs may contribute to the etiology of neurodevelopmental disorders.
- The identified miRNAs and their targets provide potential biomarkers and therapeutic targets for psychiatric conditions.
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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
MicroRNAs
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...

