RNA-based networks: using RNA aptamers and ribozymes as synthetic genetic devices

Methods Mol Biol. 2012:813:157-68. doi: 10.1007/978-1-61779-412-4_9.

Abstract

Within the last few years, a set of synthetic riboswitches has been engineered, which expands the toolbox of genetic regulatory devices. Small molecule binding aptamers have been used for the design of such riboswitches by insertion into untranslated regions of mRNAs, exploiting the fact that upon ligand binding the RNA structure interferes either with translation initiation or pre-mRNA splicing in yeast. In combination with self-cleaving ribozymes, aptamers have been used to modulate RNA stability. In this chapter, we discuss the applicability of different aptamers, ways to identify novel genetic devices, the pros and cons of various insertion sites and the application of allosteric ribozymes. Our expertise help to apply synthetic riboswitches to engineer complex genetic circuits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allosteric Regulation
  • Aptamers, Nucleotide / genetics*
  • Aptamers, Nucleotide / metabolism
  • Base Sequence
  • Genes, Essential / genetics
  • Genes, Reporter / genetics
  • HeLa Cells
  • Humans
  • Protein Biosynthesis
  • RNA Splicing / genetics
  • RNA Stability
  • RNA, Catalytic / chemistry
  • RNA, Catalytic / genetics
  • RNA, Catalytic / metabolism*
  • Riboswitch / genetics
  • Saccharomyces cerevisiae / genetics
  • Synthetic Biology / methods*

Substances

  • Aptamers, Nucleotide
  • RNA, Catalytic
  • Riboswitch