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  Altered microRNA and target gene expression related to Tetralogy of Fallot

Grunert, M., Appelt, S., Dunkel, I., Berger, F., & Sperling, S. R. (2019). Altered microRNA and target gene expression related to Tetralogy of Fallot. Scientific Reports, 9: 19063 (2019). doi:10.1038/s41598-019-55570-4.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0005-7E71-F Version Permalink: http://hdl.handle.net/21.11116/0000-0005-7E72-E
Genre: Journal Article

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 Creators:
Grunert, Marcel, Author
Appelt, Sandra1, Author              
Dunkel, Ilona2, Author              
Berger, Felix, Author
Sperling, Silke R., Author
Affiliations:
1Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              
2Regulatory Networks in Stem Cells (Edda G. Schulz), Independent Junior Research Groups (OWL), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_2117286              

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 Abstract: MicroRnAs (miRnAs) play an important role in guiding development and maintaining function of the human heart. Dysregulation of miRnAs has been linked to various congenital heart diseases including Tetralogy of Fallot (TOF), which represents the most common cyanotic heart malformation in humans. Several studies have identified dysregulated miRNAs in right ventricular (RV) tissues of TOF patients. In this study, we profiled genome-wide the whole transcriptome and analyzed the relationship of miRNAs and mRNAs of RV tissues of a homogeneous group of 22 non-syndromic TOF patients. Observed profiles were compared to profiles obtained from right and left ventricular tissue of normal hearts. To reduce the commonly observed large list of predicted target genes of dysregulated miRNAs, we applied a stringent target prediction pipeline integrating probabilities for miRNA-mRNA interaction. The final list of disease-related miRNA-mRNA pairs comprises novel as well as known miRNAs including miR-1 and miR-133, which are essential to cardiac development and function by regulating KCNJ2, FBN2, SLC38A3and TNNI1. Overall, our study provides additional insights into post-transcriptional gene regulation of malformed hearts of tof patients.

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Language(s): eng - English
 Dates: 2019-11-292019-12-13
 Publication Status: Published online
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 Identifiers: DOI: 10.1038/s41598-019-55570-4
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Title: Scientific Reports
  Abbreviation : Sci. Rep.
Source Genre: Journal
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Publ. Info: London, UK : Nature Publishing Group
Pages: - Volume / Issue: 9 Sequence Number: 19063 (2019) Start / End Page: - Identifier: ISSN: 2045-2322
CoNE: https://pure.mpg.de/cone/journals/resource/2045-2322