Abstract
The transcription factor hepatocyte nuclear factor 1β (HNF-1β) is essential for normal development of the kidney and other epithelial organs. In the developing mouse kidney, HNF-1β is required for the differentiation and patterning of immature nephrons and branching morphogenesis of the ureteric bud (UB). Here, we used ChIP-sequencing (ChIP-seq) and RNA sequencing (RNA-seq) to identify genes that are regulated by HNF-1β in embryonic mouse kidneys. ChIP-seq revealed that HNF-1β binds to 8284 sites in chromatin from E14.5 mouse kidneys. Comparison with previous ATAC-seq and histone modification studies showed that HNF-1β binding peaks colocalized with open chromatin and epigenetic marks of transcriptional activation (H3K27 acetylation, H3K4 trimethylation, H3K4 monomethylation), indicating that the binding sites were functional. To investigate the relationship between HNF-1β binding and HNF-1β-dependent gene regulation, RNA-seq was performed on UB cells purified from wild-type and HNF-1β mutant embryonic kidneys. A total of 1632 genes showed reduced expression in HNF-1β-deficient UB cells, and 485 genes contained nearby HNF-1β binding sites indicating that they were directly activated by HNF-1β. Conversely, HNF-1β directly repressed the expression of 526 genes in the UB. Comparison with snATAC-seq analysis of UB-derived cells showed that both HNF-1β-dependent activation and repression correlated with chromatin accessibility. Pathway analysis revealed that HNF-1β binds near 68 axon guidance genes in the developing kidney. RNA-seq analysis showed that Nrp1, Sema3c, Sema3d, Sema6a, and Slit2 were activated by HNF-1β, whereas Efna1, Epha3, Epha4, Epha7, Ntn4, Plxna2, Sema3a, Sema4b, Slit3, Srgap1, Unc5c and Unc5d were repressed by HNF-1β. RNAscope in situ hybridization showed that Nrp1, Sema3c, Sema3d, Sema6a, and Slit2 were expressed in wild-type UB and were dysregulated in HNF-1β mutant UB. These studies show that HNF-1β directly regulates the expression of multiple axon guidance genes in the developing mouse kidney. Dysregulation of axon guidance genes may underlie kidney defects in HNF-1β mutant mice.
| Original language | English (US) |
|---|---|
| Article number | 17586 |
| Journal | Scientific reports |
| Volume | 12 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 2022 |
Bibliographical note
Funding Information:We thank Marco Pontoglio (Institut Cochin) for providing the HNF-1β flox mice. We thank Svetlana Avdulov and Alan Mickelson for technical assistance; Karam Aboudehen and Mark Murphy for advice; Colleen Forster for histology support (Bionet, Clinical and Translational Science Institute, University of Minnesota); Rashi Arora, Therese Martin, and Nisha Shah for flow cytometry support (Flow Cytometry Resource, University of Minnesota); Aaron Becker and Elyse Froehling for next generation sequencing support (University of Minnesota Genomics Center); Juan Abrahante for assistance with RNA-seq mapping and quality analysis (University of Minnesota Informatics Institute). This work was support by National Institutes of Health grant R01DK042921.
Funding Information:
We thank Marco Pontoglio (Institut Cochin) for providing the HNF-1β flox mice. We thank Svetlana Avdulov and Alan Mickelson for technical assistance; Karam Aboudehen and Mark Murphy for advice; Colleen Forster for histology support (Bionet, Clinical and Translational Science Institute, University of Minnesota); Rashi Arora, Therese Martin, and Nisha Shah for flow cytometry support (Flow Cytometry Resource, University of Minnesota); Aaron Becker and Elyse Froehling for next generation sequencing support (University of Minnesota Genomics Center); Juan Abrahante for assistance with RNA-seq mapping and quality analysis (University of Minnesota Informatics Institute). This work was support by National Institutes of Health grant R01DK042921.
Publisher Copyright:
© 2022, The Author(s).
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