AUTHOR=Ferraz Rafaella Sousa , Santos Lucas Cauê Bezerra , da-Silva-Cruz Rebecca Lais , Braga-da-Silva Cintia Helena , Magalhães Leandro , Ribeiro-dos-Santos Arthur , Vidal Amanda , Vinasco-Sandoval Tatiana , Reis-das-Mercês Laís , Sena-dos-Santos Camille , Pereira Adenilson Leão , Silva Lilian Souza D’Albuquerque , Melo Franciane T. Cunha de , Souza Ana Carolina C. Braga de , Leal Valéria S. Galvão , Figueiredo Priscila B. Barbosa de , Neto João F. Abrahão , Moraes Lorena Vilhena de , Lemos Gabriela Nascimento de , Queiroz Natércia Neves Marques de , Felício Karem Miléo , Cavalcante Giovanna C. , Ribeiro-dos-Santos Ândrea , Felício João Soares TITLE=Global miRNA expression reveals novel nuclear and mitochondrial interactions in Type 1 diabetes mellitus JOURNAL=Frontiers in Endocrinology VOLUME=13 YEAR=2022 URL=https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2022.1033809 DOI=10.3389/fendo.2022.1033809 ISSN=1664-2392 ABSTRACT=Background

Considering the potential role of miRNAs as biomarkers and their interaction with both nuclear and mitochondrial genes, we investigated the miRNA expression profile in type 1 diabetes (T1DM) patients, including the pathways in which they are involved considering both nuclear and mitochondrial functions.

Methods

We analyzed samples of T1DM patients and control individuals (normal glucose tolerance) by high throughput miRNA sequencing (miRNome). Next, five miRNAs – hsa-miR-26b-5p, hsa-let-7i-5p, hsa-miR-143-3p, hsa-miR-501-3p and hsa-miR-100-5p – were validated by RT-qPCR. The identification of target genes was extracted from miRTarBase and mitoXplorer database. We also performed receiver operating characteristic (ROC) curves and miRNAs that had an AUC > 0.85 were considered potential biomarkers.

Results

Overall, 41 miRNAs were differentially expressed in T1DM patients compared to control. Hsa-miR-21-5p had the highest number of predicted target genes and was associated with several pathways, including insulin signaling and apoptosis. 34.1% (14/41) of the differentially expressed miRNAs also targeted mitochondrial genes, and 80.5% (33/41) of them targeted nuclear genes involved in the mitochondrial metabolism. All five validated miRNAs were upregulated in T1DM. Among them, hsa-miR-26b-5p showed AUC>0.85, being suggested as potential biomarker to T1DM.

Conclusion

Our results demonstrated 41 DE miRNAs that had a great accuracy in discriminating T1DM and control group. Furthermore, we demonstrate the influence of these miRNAs on numerous metabolic pathways, including mitochondrial metabolism. Hsa-miR-26b-5p and hsa-miR-21-5p were highlighted in our results, possibly acting on nuclear and mitochondrial dysfunction and, subsequently, T1DM dysregulation.