Cell Type-Selective Expression of Circular RNAs in Human Pancreatic Islets.
Simranjeet KaurAashiq H MirzaFlemming PociotPublished in: Non-coding RNA (2018)
Understanding distinct cell-type specific gene expression in human pancreatic islets is important for developing islet regeneration strategies and therapies to improve β-cell function in type 1 diabetes (T1D). While numerous transcriptome-wide studies on human islet cell-types have focused on protein-coding genes, the non-coding repertoire, such as long non-coding RNA, including circular RNAs, remains mostly unexplored. Here, we explored transcriptional landscape of human α-, β-, and exocrine cells from published total RNA sequencing (RNA-seq) datasets to identify circular RNAs (circRNAs). Our analysis revealed that circRNAs are highly abundant in both α- and β-cells. We identified 10,830 high-confidence circRNAs expressed in human α-, β-, and exocrine cells. The most highly expressed candidates were MAN1A2, RMST, and HIPK3 across the three cell-types. Alternate circular isoforms were observed for circRNAs in the three cell-types, indicative of potential distinct functions. Highly selective α- and β-cell circRNAs were identified, which is suggestive of their potential role in regulating β-cell function.
Keyphrases
- single cell
- rna seq
- endothelial cells
- gene expression
- long non coding rna
- type diabetes
- poor prognosis
- induced pluripotent stem cells
- pluripotent stem cells
- cell therapy
- stem cells
- randomized controlled trial
- genome wide
- dna methylation
- metabolic syndrome
- oxidative stress
- signaling pathway
- bone marrow
- insulin resistance
- weight loss
- adipose tissue
- binding protein
- glycemic control
- human health