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Verfasst von:Stojanović, Stevan Dušan [VerfasserIn]   i
 Fuchs, Maximilian [VerfasserIn]   i
 Liang, Chunguang [VerfasserIn]   i
 Schmidt, Kevin [VerfasserIn]   i
 Xiao, Ke [VerfasserIn]   i
 Just, Annette [VerfasserIn]   i
 Pfanne, Angelika [VerfasserIn]   i
 Pich, Andreas [VerfasserIn]   i
 Warnecke, Gregor [VerfasserIn]   i
 Braubach, Peter [VerfasserIn]   i
 Petzold, Christina [VerfasserIn]   i
 Jonigk, Danny [VerfasserIn]   i
 Distler, Jörg Hans Wilhelm [VerfasserIn]   i
 Fiedler, Jan [VerfasserIn]   i
 Thum, Thomas [VerfasserIn]   i
 Kunz, Meik [VerfasserIn]   i
Titel:Reconstruction of the miR-506-Quaking axis in Idiopathic Pulmonary Fibrosis using integrative multi-source bioinformatics
Verf.angabe:Stevan D. Stojanović, Maximilian Fuchs, Chunguang Liang, Kevin Schmidt, Ke Xiao, Annette Just, Angelika Pfanne, Andreas Pich, Gregor Warnecke, Peter Braubach, Christina Petzold, Danny Jonigk, Jörg H. W. Distler, Jan Fiedler, Thomas Thum, Meik Kunz
E-Jahr:2021
Jahr:Jun 14 2021
Umfang:9 S.
Fussnoten:Gesehen am 03.03.2022
Titel Quelle:Enthalten in: Scientific reports
Ort Quelle:[London] : Macmillan Publishers Limited, part of Springer Nature, 2011
Jahr Quelle:2021
Band/Heft Quelle:11(2021), Artikel-ID 12456, Seite 1-9
ISSN Quelle:2045-2322
Abstract:Abstract:The family of RNA-binding proteins (RBP) functions as a crucial regulator of multiple biological processes and diseases. However, RBP function in the clinical setting of idiopathic pulmonary fibrosis (IPF) is still unknown. We developed a practical in silico screening approach for the characterization of RBPs using multi-sources data information and comparative molecular network bioinformatics followed by wet-lab validation studies. Data mining of bulk RNA-Sequencing data of tissues of patients with IPF identified Quaking (QKI) as a significant downregulated RBP. Cell-type specific expression was confirmed by single-cell RNA-Sequencing analysis of IPF patient data. We systematically analyzed the molecular interaction network around QKI and its functional interplay with microRNAs (miRs) in human lung fibroblasts and discovered a novel regulatory miR-506-QKI axis contributing to the pathogenesis of IPF. The in silico results were validated by in-house experiments applying model systems of miR and lung biology. This study supports an understanding of the intrinsic molecular mechanisms of IPF regulated by the miR-506-QKI axis. Initially applied to human lung disease, the herein presented integrative in silico data mining approach can be adapted to other disease entities, underlining its practical relevance in RBP research.
DOI:doi:10.1038/s41598-021-89531-7
URL:Bibliographic entry. University members only receive access to full-texts for open access or licensed publications.

Volltext ; Verlag: https://doi.org/10.1038/s41598-021-89531-7
 Volltext: http://www.nature.com/articles/s41598-021-89531-7
 DOI: https://doi.org/10.1038/s41598-021-89531-7
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1794615881
Verknüpfungen:→ Journal

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