Research Resource: RNA-Seq Reveals Unique Features of the Pancreatic β-Cell Transcriptome
Author(s) -
Gregory Ku,
Hail Kim,
Ian W. Vaughn,
Matthew J. Hangauer,
ChangMyung Oh,
Michael S. German,
Michael T. McManus
Publication year - 2012
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/me.2012-1176
Subject(s) - biology , transcriptome , rna , non coding rna , intergenic region , computational biology , cell , gene , cell type , genetics , gene expression , genome
The pancreatic β-cell is critical for the maintenance of glycemic control. Knowing the compendium of genes expressed in β-cells will further our understanding of this critical cell type and may allow the identification of future antidiabetes drug targets. Here, we report the use of next-generation sequencing to obtain nearly 1 billion reads from the polyadenylated RNA of islets and purified β-cells from mice. These data reveal novel examples of β-cell-specific splicing events, promoter usage, and over 1000 long intergenic noncoding RNA expressed in mouse β-cells. Many of these long intergenic noncoding RNA are β-cell specific, and we hypothesize that this large set of novel RNA may play important roles in β-cell function. Our data demonstrate unique features of the β-cell transcriptome.
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