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Regulation of the Pancreatic Exocrine Differentiation Program and Morphogenesis by Onecut 1/Hnf6

dc.contributor.authorKropp, Peter A.
dc.contributor.authorZhu, Xiaodong
dc.contributor.authorGannon, Maureen
dc.identifier.citationKropp, P. A., Zhu, X., & Gannon, M. (2019). Regulation of the Pancreatic Exocrine Differentiation Program and Morphogenesis by Onecut 1/Hnf6. Cellular and molecular gastroenterology and hepatology, 7(4), 841–856.
dc.description.abstractBACKGROUND & AIMS: The Onecut 1 transcription factor (Oc1, a.k.a. HNF6) promotes differentiation of endocrine and duct cells of the pancreas; however, it has no known role in acinar cell differentiation. We sought to better understand the role of Oc1 in exocrine pancreas development and to identify its direct transcriptional targets. METHODS: Pancreata from Oc1(Delta panc) (Oc1(fl/fl); Pdx1-Cre) mouse embryos and neonates were analyzed morphologically. High-throughput RNA-sequencing was performed on control and Oc1-deficient pancreas; chromatin immunoprecipitation sequencing was performed on wild-type embryonic mouse pancreata to identify direct Oc1 transcriptional targets. Immunofluorescence labeling was used to confirm the RNA-sequencing/chromatin immuno precipitation sequencing results and to further investigate the effects of Oc1 loss on acinar cells. RESULTS: Loss of Oc1 from the developing pancreatic epithelium resulted in disrupted duct and acinar cell development. RNA-sequencing revealed decreased expression of acinar cell regulatory factors (Nr5a2, Ptf1a, Gata4, Mist1) and functional genes (Amylase, Cpa1, Prss1, Spink1) at embryonic day (e) 18.5 in Oc1(Delta panc) samples. Approximately 1000 of the altered genes were also identified as direct Oc1 targets by chromatin immunoprecipitation sequencing, including most of the previously noted genes. By immunolabeling, we confirmed that Amylase, Mist1, and GATA4 protein levels are significantly decreased by P2, and Spink1 protein levels were significantly reduced and mislocalized. The pancreatic duct regulatory factors Hnf1 beta and FoxA2 were also identified as direct Oc1 targets. CONCLUSIONS: These findings confirm that Oc1 is an important regulator of both duct and acinar cell development in the embryonic pancreas. Novel transcriptional targets of Oc1 have now been identified and provide clarity into the mechanisms of Oc1 transcriptional regulation in the developing exocrine pancreas. Oc1 can now be included in the gene-regulatory network of acinar cell regulatory genes. Oc1 regulates other acinar cell regulatory factors and acinar cell functional genes directly, and it can also regulate some acinar cell regulatory factors (eg, Mist1) indirectly. Oc1 therefore plays an important role in acinar cell development.en_US
dc.description.sponsorshipSupported in part by the Vanderbilt University Training Program in Stem Cell and Regenerative Developmental Biology (T32 HD05702, P.A.K.), National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Diseases R01 (DK105689, X.Z., M.G.), and by a VA Merit award (1 I01 BX003744-01, M.G.).en_US
dc.publisherCellular and Molecular Gastroenterology and Hepatologyen_US
dc.rightsCopyright © 2019 The Authors This is an open access article under the CC BY-NC-ND license (
dc.subjectPancreas Developmenten_US
dc.titleRegulation of the Pancreatic Exocrine Differentiation Program and Morphogenesis by Onecut 1/Hnf6en_US

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