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Role of circular RNAs in pancreatic β-cell physiology



           Amaresh Panda

           Institute of Life Sciences, Bhubaneswar, Odisha, India



           Diabetes      is   characterized       by    increased      blood     glucose     levels     due    to
                                                                                                         β-cells
           synthesize and secrete insulin to maintain glucose homeostasis in the body.
                               regulation

           of gene expression at transcriptional and posttranscriptional levels. Recently,
           another      class     of    ncRNAs,        called     circular     RNAs       (circRNAs)       have
           emerged as critical regulators of gene expression. Unlike linear RNAs,
           circRNA      detection     requires     detecting      the    backsplice      junction    sequence
           of circRNAs using RNA-seq or microarray or RT-PCR. Here, we aim to
           identify    circRNAs       expressed        in    the    pancreatic      islets    of    a    mouse
                             physiology  Here,
           we used published RNA-seq data of the mouse pancreatic islets with
           type 2 diabetes to identify the expression pattern of circRNAs. This
                       identi  o   m   t
           circRNAs in pancreatic islets. The expression of several circRNAs was altered

           in the islets of mice fed a high-fat diet compared to those fed a normal diet.
           Interestingly,     several     circRNAs       were     found     to    be    derived      from     the
           preproinsulin 2 (Ins2) gene. Furthermore, we validated the expression of ci-Ins2 and
           other circRNAs in mouse pancreatic islets and βTC6 cells. The computational
           analysis suggested  that these circRNAs might sponge several microRNAs, regulating
           crucial   genes   involved in various biological processes.
           T ogether,

             gene        physiology    a  u  t  a
             signifi  o  t  c  i  i  p  a  s

                                 po-
           tential to identify the critical modulators of β-cell failure and could pave the way for
           novel therapeutic strategies in diabetes.
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