Efficient dual sgRNA-directed large gene deletion in rabbit with CRISPR/Cas9 system.

Cell Mol Life Sci

Jilin Provincial Key Laboratory of Animal Embryo Engineering, Jilin University, Changchun, 130062, China.

Published: August 2016

AI Article Synopsis

  • The CRISPR/Cas9 gene-editing system is commonly used to modify genes in various organisms, but previous methods often resulted in multiple mutations within targeted genes.
  • In this study, researchers created a significant 105 kb deletion in the TYR gene of rabbits using a dual sgRNA approach, which led to albino rabbits with reduced TYR expression.
  • The deletion caused by this method was successfully passed on to the next generation without causing unintended mutations, indicating that it is a reliable approach for large genetic modifications.

Article Abstract

The CRISPR RNA-guided Cas9 nuclease gene-targeting system has been extensively used to edit the genome of several organisms. However, most mutations reported to date have been are indels, resulting in multiple mutations and numerous alleles in targeted genes. In the present study, a large deletion of 105 kb in the TYR (tyrosinase) gene was generated in rabbit via a dual sgRNA-directed CRISPR/Cas9 system. The typical symptoms of albinism accompanied significantly decreased expression of TYR in the TYR knockout rabbits. Furthermore, the same genotype and albinism phenotype were found in the F1 generation, suggesting that large-fragment deletions can be efficiently transmitted to the germline and stably inherited in offspring. Taken together, our data demonstrate that mono and biallelic large deletions can be achieved using the dual sgRNA-directed CRISPR/Cas9 system. This system produces no mosaic mutations or off-target effects, making it an efficient tool for large-fragment deletions in rabbit and other organisms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11108552PMC
http://dx.doi.org/10.1007/s00018-016-2143-zDOI Listing

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