Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene

被引:12
|
作者
Das, Debojyoti [1 ,2 ]
Das, Aniruddha [1 ,2 ]
Sahu, Mousumi [1 ]
Mishra, Smruti Sambhav [1 ]
Khan, Shaheerah [1 ]
Bejugam, Pruthvi R. [1 ]
Rout, Pranita K. [1 ]
Das, Arundhati [1 ,2 ]
Bano, Shehnaz [3 ]
Mishra, Gyan Prakash [1 ]
Raghav, Sunil K. [1 ]
Dixit, Anshuman [1 ]
Panda, Amaresh C. [1 ]
机构
[1] Inst Life Sci ILS, Nalco Sq, Bhubaneswar 751023, Odisha, India
[2] KIIT Univ, Sch Biotechnol, Bhubaneswar 751024, Odisha, India
[3] Natl Ctr Cell Sci NCCS, Pune 411007, Maharashtra, India
基金
英国惠康基金;
关键词
pancreatic beta-cells; lariat-derived circRNA; insulin splicing; translation; diabetes; BETA-CELL; EXPRESSION; BIOGENESIS; TRANSCRIPTION; INHIBITION; PALMITATE; LANDSCAPE;
D O I
10.3390/ijms21124302
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circular RNAs (circRNAs) are a large family of noncoding RNAs that have emerged as novel regulators of gene expression. However, little is known about the function of circRNAs in pancreatic beta-cells. Here, transcriptomic analysis of mice pancreatic islet RNA-sequencing data identified 77 differentially expressed circRNAs between mice fed with a normal diet and a high-fat diet. Surprisingly, multiple circRNAs were derived from the intron 2 of the preproinsulin 2 (Ins2) gene and are termed as circular intronic (ci)-Ins2. The expression ofci-Ins2transcripts in mouse pancreatic islets, and beta TC6 cells were confirmed by reverse transcription PCR, DNA sequencing, and RNase R treatment experiments. The level ofci-Ins2was altered in beta TC6 cells upon exposure to elevated levels of palmitate and glucose. Computational analysis predicted the interaction of several RNA-binding proteins withci-Ins2and their flanking region, suggesting their role in theci-Ins2function or biogenesis. Additionally, bioinformatics analysis predicted the association of several microRNAs withci-Ins2. Gene ontology and pathway analysis of genes targeted by miRNAs associated withci-Ins2suggested the regulation of several key biological processes. Together, our findings indicate that differential expression of circRNAs, especiallyci-Ins2transcripts, may regulate beta-cell function and may play a critical role in the development of diabetes.
引用
收藏
页码:1 / 17
页数:17
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