Abstract
Pancreatic β cells are responsible for maintaining glucose homeostasis; their absence or malfunction results in diabetes mellitus. Although there is evidence that long noncoding RNAs (lncRNAs) play important roles in development and disease, none have been investigated in vivo in the context of pancreas development. In this study, we demonstrate that βlinc1 (β-cell long intergenic noncoding RNA 1), a conserved lncRNA, is necessary for the specification and function of insulin-producing β cells through the coordinated regulation of a number of islet-specific transcription factors located in the genomic vicinity of βlinc1. Furthermore, deletion of βlinc1 results in defective islet development and disruption of glucose homeostasis in adult mice.
| Original language | English |
|---|---|
| Pages (from-to) | 502-507 |
| Number of pages | 6 |
| Journal | Genes & Development |
| Volume | 30 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 1 Mar 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Animals
- Cell Line
- Endocrine System
- Gene Expression Regulation, Developmental
- Gene Knockout Techniques
- Glucose Intolerance
- Humans
- Insulin-Secreting Cells
- Mice
- Mice, Inbred C57BL
- RNA, Long Noncoding
- Transcription Factors
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't
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