Long non-coding RNAs (lncRNAs) are emerging as crucial regulators of beta cell function. Here, we show that an lncRNA-transcribed antisense to Pax6, annotated as Pax6os1/PAX6-AS1, was upregulated by high glucose concentrations in human as well as murine beta cell lines and islets. Elevated expression was also observed in islets from mice on a high-fat diet and patients with type 2 diabetes. Silencing Pax6os1/PAX6-AS1 in MIN6 or EndoC-βH1 cells increased several beta cell signature genes’ expression. Pax6os1/PAX6-AS1 was shown to bind to EIF3D, indicating a role in translation of specific mRNAs, as well as histones H3 and H4, suggesting a role in histone modifications. Important interspecies differences were found, with a stronger phenotype in humans. Only female Pax6os1 null mice fed a high-fat diet showed slightly enhanced glucose clearance. In contrast, silencing PAX6-AS1 in human islets enhanced glucose-stimulated insulin secretion and increased calcium dynamics, whereas overexpression of the lncRNA resulted in the opposite phenotype.
Roles for the long non-coding RNA Pax6os1/PAX6-AS1 in pancreatic beta cell function / Lopez-Noriega, L.; Callingham, R.; Martinez-Sanchez, A.; Nawaz, S.; Pizza, G.; Haberman, N.; Cvetesic, N.; Nguyen-Tu, M. -S.; Lenhard, B.; Marchetti, P.; Piemonti, L.; de Koning, E.; Shapiro, A. M. J.; Johnson, P. R.; Leclerc, I.; Hastoy, B.; Gauthier, B. R.; Pullen, T. J.; Rutter, G. A.. - In: ISCIENCE. - ISSN 2589-0042. - 28:1(2025). [10.1016/j.isci.2024.111518]
Roles for the long non-coding RNA Pax6os1/PAX6-AS1 in pancreatic beta cell function
Piemonti L.;
2025-01-01
Abstract
Long non-coding RNAs (lncRNAs) are emerging as crucial regulators of beta cell function. Here, we show that an lncRNA-transcribed antisense to Pax6, annotated as Pax6os1/PAX6-AS1, was upregulated by high glucose concentrations in human as well as murine beta cell lines and islets. Elevated expression was also observed in islets from mice on a high-fat diet and patients with type 2 diabetes. Silencing Pax6os1/PAX6-AS1 in MIN6 or EndoC-βH1 cells increased several beta cell signature genes’ expression. Pax6os1/PAX6-AS1 was shown to bind to EIF3D, indicating a role in translation of specific mRNAs, as well as histones H3 and H4, suggesting a role in histone modifications. Important interspecies differences were found, with a stronger phenotype in humans. Only female Pax6os1 null mice fed a high-fat diet showed slightly enhanced glucose clearance. In contrast, silencing PAX6-AS1 in human islets enhanced glucose-stimulated insulin secretion and increased calcium dynamics, whereas overexpression of the lncRNA resulted in the opposite phenotype.File | Dimensione | Formato | |
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