m6A Methylated Long Noncoding RNA LOC339803 Regulates Intestinal Inflammatory Response

Author:

Olazagoitia‐Garmendia Ane123,Rojas‐Márquez Henar23,Sebastian‐delaCruz Maialen23,Agirre‐Lizaso Aloña4,Ochoa Anne3,Mendoza‐Gomez Luis Manuel12,Perugorria Maria J456,Bujanda Luis456,Madrigal Alain Huerta278,Santin Izortze129,Castellanos‐Rubio Ainara23910ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology University of the Basque Country UPV/EHU Leioa 48940 Spain

2. Biobizkaia Health Research Institute Barakaldo 48903 Spain

3. Department of Genetics Physical Anthropology and Animal Physiology University of the Basque Country UPV/EHU Leioa 48940 Spain

4. Department of Liver and Gastrointestinal Diseases Biogipuzkoa Health Research Institute Donostia University Hospital Donostia‐San Sebastian 20014 Spain

5. Department of Medicine Faculty of Medicine and Nursing University of the Basque Country UPV/EHU Donostia‐San Sebastián 20014 Spain

6. CIBERehd Instituto de Salud Carlos III (ISCIII) Madrid 28029 Spain

7. Department of Medicine Medicine Faculty University of the Basque Country UPV/EHU Leioa 48940 Spain

8. Gastroenterology Department Hospital Universitario de Galdakao Galdakao 48960 Spain

9. Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas CIBERDEM Instituto de Salud Carlos III Madrid 28029 Spain

10. Ikerbasque Basque Foundation for Science Bilbao 48011 Spain

Abstract

AbstractCytokine mediated sustained inflammation increases the risk to develop different complex chronic inflammatory diseases, but the implicated mechanisms remain unclear. Increasing evidence shows that long noncoding RNAs (lncRNAs) play key roles in the pathogenesis of inflammatory disorders, while inflammation associated variants are described to affect their function or essential RNA modifications as N6‐methyladenosine (m6A) methylation, increasing predisposition to inflammatory diseases. Here, the functional implication of the intestinal inflammation associated lncRNA LOC339803 in the production of cytokines by intestinal epithelial cells is described. Allele‐specific m6A methylation is found to affect YTHDC1 mediated protein binding affinity. LOC339803‐YTHDC1 interaction dictates chromatin localization of LOC339803 ultimately inducing the expression of NFκB mediated proinflammatory cytokines and contributing to the development of intestinal inflammation. These findings are confirmed using human intestinal biopsy samples from different intestinal inflammatory conditions and controls. Additionally, it is demonstrated that LOC339803 targeting can be a useful strategy for the amelioration of intestinal inflammation in vitro and ex vivo. Overall, the results support the importance of the methylated LOC339803 lncRNA as a mediator of intestinal inflammation, explaining genetic susceptibility and presenting this lncRNA as a potential novel therapeutic target for the treatment of inflammatory intestinal disorders.

Funder

European Foundation for the Study of Diabetes

Euskal Herriko Unibertsitatea

Eusko Jaurlaritza

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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