Abstract:
The CRISPR-Cas9 genome editing system is a molecular tool that can be used to introduce precise changes into the genomes of model and
non-model species alike. This technology can be used for a variety of genome editing approaches, from gene knockouts and knockins to more
specific changes like the introduction of a few nucleotides at a targeted location. Genome editing can be used for a multitude of applications,
including the partial functional characterization of genes, the production of transgenic organisms and the development of diagnostic tools.
Compared to previously available gene editing strategies, the CRISPR-Cas9 system has been shown to be easy to establish in new species and
boasts high efficiency and specificity. The primary reason for this is that the editing tool uses an RNA molecule to target the gene or sequence of
interest, making target molecule design straightforward, given that standard base pairing rules can be exploited. Similar to other genome editing
systems, CRISPR-Cas9-based methods also require efficient and effective transformation protocols as well as access to good quality sequence
data for the design of the targeting RNA and DNA molecules. Since the introduction of this system in 2013, it has been used to genetically
engineer a variety of model species, including Saccharomyces cerevisiae, Arabidopsis thaliana, Drosophila melanogaster and Mus musculus.
Subsequently, researchers working on non-model species have taken advantage of the system and used it for the study of genes involved in
processes as diverse as secondary metabolism in fungi, nematode growth and disease resistance in plants, among many others. This protocol
detailed below describes the use of the CRISPR-Cas9 genome editing protocol for the truncation of a gene involved in the sexual cycle of
Huntiella omanensis, a filamentous ascomycete fungus belonging to the Ceratocystidaceae family.
