Constructing GFP-Based Reporter to Study Back Splicing and Translation of Circular RNA

Methods Mol Biol. 2018:1724:107-118. doi: 10.1007/978-1-4939-7562-4_9.

Abstract

Human transcriptome contains a large number of circular RNAs (circRNAs) that are mainly produced by back splicing of pre-mRNA. Here we describe a minigene reporter system containing a single exon encoding split GFP in reverse order, which can be efficiently back spliced to produce a circRNA encoding intact GFP gene. This simple reporter system can be adopted to study how different cis-elements and trans-factors affect circRNA production, and also can serve as a reliable system to measure the activity of IRES-mediated translation. Therefore this system can serve as a platform for mechanistic studies on the circRNA biogenesis and its function.

Keywords: Back-splicing; Cap-independent translation; Circular RNA; Internal ribosomal entry sites; Splicing reporter.

MeSH terms

  • Alternative Splicing*
  • Gene Expression Regulation*
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism*
  • Humans
  • Internal Ribosome Entry Sites
  • Protein Biosynthesis*
  • RNA / genetics
  • RNA / metabolism*
  • RNA, Circular
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Regulatory Elements, Transcriptional*

Substances

  • Internal Ribosome Entry Sites
  • RNA, Circular
  • RNA, Messenger
  • Green Fluorescent Proteins
  • RNA