Correlation Engine 2.0
Clear Search sequence regions


  • 3 utr (1)
  • dnase (3)
  • elements (1)
  • gene circuits (2)
  • genes (1)
  • mrna (3)
  • pre- mrna (1)
  • rna (3)
  • target gene (1)
  • Sizes of these terms reflect their relevance to your search.

    We describe a new way to trigger mRNA degradation in Saccharomyces cerevisiae synthetic gene circuits. Our method demands to modify either the 5'- or the 3'-UTR that flanks a target gene with elements from the pre-crRNA of type V Cas12a proteins and expresses a DNase-deficient Cas12a (dCas12a). dCas12a recognizes and cleaves the pre-crRNA motifs on mRNA sequences. Our tool does not require complex engineering operations and permits an efficient control of protein expression via mRNA degradation. © 2024. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

    Citation

    Lifang Yu, Mario Andrea Marchisio. dCas12a:Pre-crRNA: A New Tool to Induce mRNA Degradation in Saccharomyces cerevisiae Synthetic Gene Circuits. Methods in molecular biology (Clifton, N.J.). 2024;2760:95-114

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 38468084

    View Full Text