Correction of a Factor VIII genomic inversion with designer-recombinases

Nat Commun. 2022 Jan 20;13(1):422. doi: 10.1038/s41467-022-28080-7.

Abstract

Despite advances in nuclease-based genome editing technologies, correcting human disease-causing genomic inversions remains a challenge. Here, we describe the potential use of a recombinase-based system to correct the 140 kb inversion of the F8 gene frequently found in patients diagnosed with severe Hemophilia A. Employing substrate-linked directed molecular evolution, we develop a coupled heterodimeric recombinase system (RecF8) achieving 30% inversion of the target sequence in human tissue culture cells. Transient RecF8 treatment of endothelial cells, differentiated from patient-derived induced pluripotent stem cells (iPSCs) of a hemophilic donor, results in 12% correction of the inversion and restores Factor VIII mRNA expression. In this work, we present designer-recombinases as an efficient and specific means towards treatment of monogenic diseases caused by large gene inversions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cell Differentiation
  • Chromosome Inversion / genetics*
  • Clone Cells
  • Directed Molecular Evolution
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism
  • Exons / genetics
  • Factor VIII / genetics*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Inverted Repeat Sequences / genetics
  • Recombinases / metabolism*
  • Recombination, Genetic / genetics
  • Substrate Specificity
  • Whole Genome Sequencing

Substances

  • Recombinases
  • Factor VIII