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Independent component and pathway-based analysis of miRNA-regulated gene expression in a model of type 1 diabetes.

Bang-Berthelsen CH, Pedersen L, Fløyel T, Hagedorn PH, Gylvin T, Pociot F - BMC Genomics (2011)

Bottom Line: Applying ICA on the mRNA profiling data revealed five significant independent components (ICs) correlating to the experimental conditions.By using ICA, seven of the eight miRNAs showed significant enrichment of sequence predicted targets, compared to only four miRNAs when using simple negative correlation.The results suggest that ICA is better at identifying miRNA targets than negative correlation.

View Article: PubMed Central - HTML - PubMed

Affiliation: Glostrup Research Institute, Glostrup University Hospital, DK-2600 Glostrup, Denmark.

ABSTRACT

Background: Several approaches have been developed for miRNA target prediction, including methods that incorporate expression profiling. However the methods are still in need of improvements due to a high false discovery rate. So far, none of the methods have used independent component analysis (ICA). Here, we developed a novel target prediction method based on ICA that incorporates both seed matching and expression profiling of miRNA and mRNA expressions. The method was applied on a cellular model of type 1 diabetes.

Results: Microarray profiling identified eight miRNAs (miR-124/128/192/194/204/375/672/708) with differential expression. Applying ICA on the mRNA profiling data revealed five significant independent components (ICs) correlating to the experimental conditions. The five ICs also captured the miRNA expressions by explaining > 97% of their variance. By using ICA, seven of the eight miRNAs showed significant enrichment of sequence predicted targets, compared to only four miRNAs when using simple negative correlation. The ICs were enriched for miRNA targets that function in diabetes-relevant pathways e.g. type 1 and type 2 diabetes and maturity onset diabetes of the young (MODY).

Conclusions: In this study, ICA was applied as an attempt to separate the various factors that influence the mRNA expression in order to identify miRNA targets. The results suggest that ICA is better at identifying miRNA targets than negative correlation. Additionally, combining ICA and pathway analysis constitutes a means for prioritizing between the predicted miRNA targets. Applying the method on a model of type 1 diabetes resulted in identification of eight miRNAs that appear to affect pathways of relevance to disease mechanisms in diabetes.

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Related in: MedlinePlus

Pdx-1 induction in the INSrαβ cell line. Fold changes (mean and standard deviations) in Pdx-1 protein and mRNA after treatment with doxycycline (dox) for 24 h. The gels to the right represent Pdx-1 and β-actin induction with and without dox stimulation for 24 h.
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Figure 1: Pdx-1 induction in the INSrαβ cell line. Fold changes (mean and standard deviations) in Pdx-1 protein and mRNA after treatment with doxycycline (dox) for 24 h. The gels to the right represent Pdx-1 and β-actin induction with and without dox stimulation for 24 h.

Mentions: The dox-induced Pdx-1 expression was examined using qPCR and western blotting with mouse-specific primers and antibody, respectively. We found that dox treatment for 24 hours resulted in increased expression of both Pdx-1 mRNA (33 fold, p < 0.05) and protein (6 fold, p < 0.05) (Figure 1).


Independent component and pathway-based analysis of miRNA-regulated gene expression in a model of type 1 diabetes.

Bang-Berthelsen CH, Pedersen L, Fløyel T, Hagedorn PH, Gylvin T, Pociot F - BMC Genomics (2011)

Pdx-1 induction in the INSrαβ cell line. Fold changes (mean and standard deviations) in Pdx-1 protein and mRNA after treatment with doxycycline (dox) for 24 h. The gels to the right represent Pdx-1 and β-actin induction with and without dox stimulation for 24 h.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3040732&req=5

Figure 1: Pdx-1 induction in the INSrαβ cell line. Fold changes (mean and standard deviations) in Pdx-1 protein and mRNA after treatment with doxycycline (dox) for 24 h. The gels to the right represent Pdx-1 and β-actin induction with and without dox stimulation for 24 h.
Mentions: The dox-induced Pdx-1 expression was examined using qPCR and western blotting with mouse-specific primers and antibody, respectively. We found that dox treatment for 24 hours resulted in increased expression of both Pdx-1 mRNA (33 fold, p < 0.05) and protein (6 fold, p < 0.05) (Figure 1).

Bottom Line: Applying ICA on the mRNA profiling data revealed five significant independent components (ICs) correlating to the experimental conditions.By using ICA, seven of the eight miRNAs showed significant enrichment of sequence predicted targets, compared to only four miRNAs when using simple negative correlation.The results suggest that ICA is better at identifying miRNA targets than negative correlation.

View Article: PubMed Central - HTML - PubMed

Affiliation: Glostrup Research Institute, Glostrup University Hospital, DK-2600 Glostrup, Denmark.

ABSTRACT

Background: Several approaches have been developed for miRNA target prediction, including methods that incorporate expression profiling. However the methods are still in need of improvements due to a high false discovery rate. So far, none of the methods have used independent component analysis (ICA). Here, we developed a novel target prediction method based on ICA that incorporates both seed matching and expression profiling of miRNA and mRNA expressions. The method was applied on a cellular model of type 1 diabetes.

Results: Microarray profiling identified eight miRNAs (miR-124/128/192/194/204/375/672/708) with differential expression. Applying ICA on the mRNA profiling data revealed five significant independent components (ICs) correlating to the experimental conditions. The five ICs also captured the miRNA expressions by explaining > 97% of their variance. By using ICA, seven of the eight miRNAs showed significant enrichment of sequence predicted targets, compared to only four miRNAs when using simple negative correlation. The ICs were enriched for miRNA targets that function in diabetes-relevant pathways e.g. type 1 and type 2 diabetes and maturity onset diabetes of the young (MODY).

Conclusions: In this study, ICA was applied as an attempt to separate the various factors that influence the mRNA expression in order to identify miRNA targets. The results suggest that ICA is better at identifying miRNA targets than negative correlation. Additionally, combining ICA and pathway analysis constitutes a means for prioritizing between the predicted miRNA targets. Applying the method on a model of type 1 diabetes resulted in identification of eight miRNAs that appear to affect pathways of relevance to disease mechanisms in diabetes.

Show MeSH
Related in: MedlinePlus