bioRxivDevelopmental BiologyPreprint
Human organoid modeling of congenital malformations caused by RFX6 mutations reveal an essential role for this transcription factor in establishing and maintaining duodenal identity upstream of PDX1
Jefferson G. Sanchez, Scott Rankin, Emily Paul, Heather A. McCauleyiD, Daniel O. KecheleiD, Jacob R. EnriqueziD, Nana‐Hawa Yayah JonesiD, Siri Atma W. GreeleyiD, Lisa Letourneau-Friedberg, Aaron M. ZorniD, Mansa KrishnamurthyiD, James M. WellsiD
Abstract
The gastrointestinal (GI) tract consists of highly specialized organs from the proximal esophagus to the distal colon, each with unique functions. Rare congenital malformations of the GI tract, including organ atresia, agenesis or mis-patterning are linked to gene mutations although the molecular basis of these malformations has been poorly studied due to lack of model systems to study human development. We identified a patient with compound heterozygous mutations in the transcription factor RFX6 with pancreatic agenesis as previously described. In addition, the patient had duodenal mal-rotation and atresia suggesting that establishment of the proximal small intestine was impaired in these patients. To identify the molecular basis of the intestinal malformation we generated induced pluripotent stem cell lines from this patient, and derived human intestinal organoid (HIOs) to identify how mutations in RFX6 impact intestinal patterning and function. We identified that the duodenal identity of HIOs and patient tissues had adopted a more distal small intestinal signature, including expression of SATB2, normally expressed in the ileum and colon. CRISPR-mediated correction of RFX6 restored duodenal identity, including expression of PDX1, which is required for duodenal development. Using transcriptomic approaches in HIOs and Xenopus embryos we identified that PDX1 is a downstream transcriptional target of RFX6 and that PDX1 expression in a RFX6 mutant background was sufficient to rescue duodenal identity. However, RFX6 had a PDX1-independent role in regulating expression of components of WNT, HH, and BMP signaling pathways that are critical for establishing early regional identity in the GI tract. In summary, we have identified that RFX6 is one of the most upstream regulators early intestinal patterning in vertebrates and that it acts by regulating key transcriptional and signaling pathways.
- organism: human
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: drug response / drug discovery
- approach: experimental assay
- Citations
- 2
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Deletion of RFX6, a Diabetes-Associated Gene, Impairs iPSC-Derived Islet Organoid Development and Survival, With No Impact on the Generation of PDX1+/NKX6.1+ Progenitors
Noura Aldous, Ahmed Kamel Elsayed, … Essam Mohamed Abdelalim·bioRxiv·Mar 6, 2024
- The Axenfeld-Rieger syndrome gene FOXC1 contributes to left-right patterning
Paul W. Chrystal, Curtis R. French, … Andrew Jan Waskiewicz·GenesPeer-reviewed·Jan 26, 2021
- Rfx6 promotes the differentiation of peptide-secreting enteroendocrine cells while repressing genetic programs controlling serotonin production
Julie Piccand, Constance Vagne, … Gérard Gradwohl·Molecular MetabolismPeer-reviewed·Aug 13, 2019
- Using Human Induced Pluripotent Stem Cell Derived Organoids to Identify New Pathologies in Patients with PDX1 Mutations
Mansa Krishnamurthy, Daniel O. Kechele, … James M. Wells·bioRxiv·Apr 25, 2021
- Development of rat organoids to study intestinal adaptations after Roux-en-Y Gastric Bypass
S. Benhaddou, L. Ribeiro-Parenti, … P. Larraufie·bioRxiv·Feb 24, 2024
- Engineered dual-gastruloid model for foregut-pharyngeal mesoderm co-development
Giada Mura, Michiel Tawdarous, … Shahragim Tajbakhsh·bioRxiv·Sep 28, 2026