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Published on: January 7, 2019
Identifying functional miRNA-mRNA regulatory modules with correspondence latent dirichlet allocation
Bing Liu1, Lin Liu, Anna Tsykin
1School of Computer and Information Science, University of South Australia, Mawson Lakes, SA, Australia. bing.liu@unisa.edu.au
Bioinformatics (Oxford, England)
|October 20, 2010
Summary
This study introduces a new model to find microRNA (miRNA) regulatory networks. The model effectively identifies miRNA and mRNA modules involved in biological processes using expression data.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression, controlling mRNA degradation and translation.
- Despite their importance in development and homeostasis, many miRNA functions and regulatory mechanisms remain unclear.
- Integrating miRNA and mRNA expression profiles offers a powerful approach to uncover miRNA regulatory networks.
Purpose of the Study:
- To develop a probabilistic graphical model for discovering functional miRNA regulatory modules.
- To integrate heterogeneous datasets, including miRNA and mRNA expression profiles, with or without prior target information.
- To identify miRNA-mRNA networks involved in specific biological processes.
Main Methods:
- Developed a probabilistic graphical model for module discovery.
- Integrated miRNA and mRNA expression profiles.
- Applied the model to a mouse mammary gland dataset.
Main Results:
- Successfully captured several biological process-specific miRNA regulatory modules.
- Demonstrated that expression profiles are crucial for identifying miRNA targets and regulatory modules.
- Modules identified without prior target information showed significant overlap with predicted miRNA-target relationships.
Conclusions:
- The developed model effectively discovers functional miRNA regulatory modules.
- Expression profiles are vital for understanding miRNA functions and regulatory networks.
- This approach aids in elucidating complex biological processes regulated by miRNAs.
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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...
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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...
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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...
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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA (lncRNA)...
