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Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia

Autosomal dominant polycystic kidney disease (ADPKD) affects more than 12 million people worldwide. Mutations in PKD1 and PKD2 cause cyst formation through unknown mechanisms. To unravel the pathogenic mechanisms in ADPKD, multiple studies have investigated transcriptional mis-regulation in cystic k...

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Autores principales: Friedrich, Sebastian, Müller, Hannah, Riesterer, Caroline, Schüller, Hannah, Friedrich, Katja, Wörner, Carlotta Leonie, Busch, Tilman, Viau, Amandine, Kuehn, E. Wolfgang, Köttgen, Michael, Hofherr, Alexis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302622/
https://www.ncbi.nlm.nih.gov/pubmed/34301992
http://dx.doi.org/10.1038/s41598-021-94442-8
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author Friedrich, Sebastian
Müller, Hannah
Riesterer, Caroline
Schüller, Hannah
Friedrich, Katja
Wörner, Carlotta Leonie
Busch, Tilman
Viau, Amandine
Kuehn, E. Wolfgang
Köttgen, Michael
Hofherr, Alexis
author_facet Friedrich, Sebastian
Müller, Hannah
Riesterer, Caroline
Schüller, Hannah
Friedrich, Katja
Wörner, Carlotta Leonie
Busch, Tilman
Viau, Amandine
Kuehn, E. Wolfgang
Köttgen, Michael
Hofherr, Alexis
author_sort Friedrich, Sebastian
collection PubMed
description Autosomal dominant polycystic kidney disease (ADPKD) affects more than 12 million people worldwide. Mutations in PKD1 and PKD2 cause cyst formation through unknown mechanisms. To unravel the pathogenic mechanisms in ADPKD, multiple studies have investigated transcriptional mis-regulation in cystic kidneys from patients and mouse models, and numerous dysregulated genes and pathways have been described. Yet, the concordance between studies has been rather limited. Furthermore, the cellular and genetic diversity in cystic kidneys has hampered the identification of mis-expressed genes in kidney epithelial cells with homozygous PKD mutations, which are critical to identify polycystin-dependent pathways. Here we performed transcriptomic analyses of Pkd1- and Pkd2-deficient mIMCD3 kidney epithelial cells followed by a meta-analysis to integrate all published ADPKD transcriptomic data sets. Based on the hypothesis that Pkd1 and Pkd2 operate in a common pathway, we first determined transcripts that are differentially regulated by both genes. RNA sequencing of genome-edited ADPKD kidney epithelial cells identified 178 genes that are concordantly regulated by Pkd1 and Pkd2. Subsequent integration of existing transcriptomic studies confirmed 31 previously described genes and identified 61 novel genes regulated by Pkd1 and Pkd2. Cluster analyses then linked Pkd1 and Pkd2 to mRNA splicing, specific factors of epithelial mesenchymal transition, post-translational protein modification and epithelial cell differentiation, including CD34, CDH2, CSF2RA, DLX5, HOXC9, PIK3R1, PLCB1 and TLR6. Taken together, this model-based integrative analysis of transcriptomic alterations in ADPKD annotated a conserved core transcriptomic profile and identified novel candidate genes for further experimental studies.
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spelling pubmed-83026222021-07-27 Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia Friedrich, Sebastian Müller, Hannah Riesterer, Caroline Schüller, Hannah Friedrich, Katja Wörner, Carlotta Leonie Busch, Tilman Viau, Amandine Kuehn, E. Wolfgang Köttgen, Michael Hofherr, Alexis Sci Rep Article Autosomal dominant polycystic kidney disease (ADPKD) affects more than 12 million people worldwide. Mutations in PKD1 and PKD2 cause cyst formation through unknown mechanisms. To unravel the pathogenic mechanisms in ADPKD, multiple studies have investigated transcriptional mis-regulation in cystic kidneys from patients and mouse models, and numerous dysregulated genes and pathways have been described. Yet, the concordance between studies has been rather limited. Furthermore, the cellular and genetic diversity in cystic kidneys has hampered the identification of mis-expressed genes in kidney epithelial cells with homozygous PKD mutations, which are critical to identify polycystin-dependent pathways. Here we performed transcriptomic analyses of Pkd1- and Pkd2-deficient mIMCD3 kidney epithelial cells followed by a meta-analysis to integrate all published ADPKD transcriptomic data sets. Based on the hypothesis that Pkd1 and Pkd2 operate in a common pathway, we first determined transcripts that are differentially regulated by both genes. RNA sequencing of genome-edited ADPKD kidney epithelial cells identified 178 genes that are concordantly regulated by Pkd1 and Pkd2. Subsequent integration of existing transcriptomic studies confirmed 31 previously described genes and identified 61 novel genes regulated by Pkd1 and Pkd2. Cluster analyses then linked Pkd1 and Pkd2 to mRNA splicing, specific factors of epithelial mesenchymal transition, post-translational protein modification and epithelial cell differentiation, including CD34, CDH2, CSF2RA, DLX5, HOXC9, PIK3R1, PLCB1 and TLR6. Taken together, this model-based integrative analysis of transcriptomic alterations in ADPKD annotated a conserved core transcriptomic profile and identified novel candidate genes for further experimental studies. Nature Publishing Group UK 2021-07-23 /pmc/articles/PMC8302622/ /pubmed/34301992 http://dx.doi.org/10.1038/s41598-021-94442-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Friedrich, Sebastian
Müller, Hannah
Riesterer, Caroline
Schüller, Hannah
Friedrich, Katja
Wörner, Carlotta Leonie
Busch, Tilman
Viau, Amandine
Kuehn, E. Wolfgang
Köttgen, Michael
Hofherr, Alexis
Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
title Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
title_full Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
title_fullStr Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
title_full_unstemmed Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
title_short Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
title_sort identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302622/
https://www.ncbi.nlm.nih.gov/pubmed/34301992
http://dx.doi.org/10.1038/s41598-021-94442-8
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