Project Details
Projekt
Clonal evolution of somatic mosaicism during acute-to-chronic kidney disease progression
Applicants
Dr. Ashley Sanders; Professor Dr. Kai Schmidt-Ott
Subject Area
Nephrology
Cell Biology
Cell Biology
Term
since 2023
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 400728090
Acute kidney injury is commonly observed in critically ill individuals and results in a greatly increased risk of progressive chronic kidney disease or death. Acute kidney injury is initiated by complex pathophysiological processes that include inflammation, ischemia, hypoxia, and/or toxin exposure. Acute kidney injury results in widespread cell death of the cells of the renal tubule. Surviving cells then proliferate clonally and repair the injured kidney tubule. The repeated cycles of cellular stress, injury, proliferation, and recovery may predispose kidney cells to disease-promoting somatic mutations. Somatic mutations in renal cells can generate genetically distinct cell populations (i.e., subclones) that result in tissue-specific ‘somatic mosaicism’. When these mutations disrupt key epigenetic and transcriptional programs, they can give rise to pathogenic subclones with distinct disease phenotypes and mechanisms. This hypothesis is supported by evidence of increased genomic instability in kidney disease and by the propensity of patients with acute kidney injury or chronic kidney disease to develop renal tumors. However, the role of acquired somatic mosaicism in kidney tissue and its potential pathophysiological implications are incompletely understood. Here, we propose to combine single-cell and strand-specific DNA sequencing (i.e., Strand-seq) with assay for transposase-accessible chromatin (ATAC) and single-nucleus RNA sequencing from kidney cells and tissues to investigate the development and consequences of somatic mosaicism at the single-cell level. We will identify the types and frequency of acquired somatic structural variants such as deletions, insertions, inversions, and other genomic rearrangements and correlate them with changes in genome-wide nucleosome occupancy, chromatin accessibility, and gene expression in kidney cells. We will compare experimental conditions (in vivo ischemia-reperfusion injury in mouse kidneys and in vitro simulated hypoxia of kidney cells) and clinical samples of kidney cells excreted in urine from patients with acute or chronic kidney disease. The putative effects of somatic structural variants on renal cell proliferation, cell death, and gene expression will be validated by experimental modeling of variant-associated molecular perturbations in kidney cells. The study has the potential to uncover novel molecular links between acquired somatic genomic alterations in kidney cells and disease-promoting dysregulation of gene expression control.
DFG Programme
Research Units
