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Effects of the timing of electroporation during maturation on triple gene editing in porcine embryos using CRISPR/Cas9 system. | LitMetric

AI Article Synopsis

  • The study investigates the impact of the timing of electroporation on gene editing efficiency in pig oocytes, hypothesizing that earlier electroporation could enhance mutation rates due to increased permeability.
  • Results showed that electroporation at 40 h and 42 h during maturation reduced blastocyst formation rates without improving mutation rates, while treatment at 44 h yielded similar results to control zygotes electroporated after fertilization.
  • The findings suggest that electroporating mature oocytes does not significantly enhance multiple gene editing efficiency compared to zygotes, highlighting that fully matured oocytes may offer similar gene editing potential as zygotes.

Article Abstract

Mosaicism, including alleles comprising both wild-type and mutant, is a serious problem for gene modification by gene editing using electroporation. One-step generation of F0 pigs with completely desired gene modifications saves cost and time, but the major obstacles have been mosaic mutations. We hypothesized that the timing of electroporation prior to fertilization (IVF) can increase the rates of biallelic mutation for multiple gene knockout as the permeability of mature oocytes is greater than that of zygotes. Hence, we determined whether the timing of electroporation during maturation (IVM) culture enhances triple gene editing in the resulting blastocysts. Three gRNAs targeting , and were simultaneously introduced into the oocytes that had been incubated for 40, 42, and 44 h from the start of the IVM culture. Electroporation with three gRNAs at 40 h and 42 h during IVM culture decreased the blastocyst formation rates and did not improve the mutation rates and target number of biallelic mutations in the resulting blastocysts. The blastocyst formation rate, mutation rates, and target numbers in the resulting blastocysts from oocytes treated by electroporation at 44 h of IVM culture were similar to those of control zygotes electroporated at 13 h after the initiation of IVF. In conclusion, multiple gene editing efficiency in the resulting blastocysts was comparable between oocytes electroporated before and after the fertilization, indicating that oocytes with completed maturation time may allow better functioning of materials accepting gene editing application.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899406PMC
http://dx.doi.org/10.1016/j.vas.2022.100241DOI Listing

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