Scientists have developed a strategy for editing and repairing a particular type of genetic mutation associated with microduplications using CRISPR/Cas9 and a seldom-used DNA repair pathway. Described in Nature, this approach to programmable gene editing overcomes prior inefficiencies in gene correction.
"It's like hitting the reset button," said the senior author. "We don't have to add any corrective genetic material, instead the cell stitches the DNA back together minus the duplication. It's a shortcut for gene correction with potential therapeutic appeal."
Microduplications are changes in chromosomes where small segments of DNA are copied or duplicated. In certain genes, these duplications can lead to what are called "frameshift mutations," when the number of added nucleotides is not divisible by three. This alters the translation of gene into protein, causing a loss of function. Frameshift mutations resulting from microduplications cause as many as 143 different diseases, including limb-girdle muscular dystrophy, Hermansky-Pudlak syndrome, and Tay-Sachs.
Most of the gene editing techniques require both generating a break of the DNA strands at the defective gene and the introduction of corrective genetic material. The new sequence is inserted into the break and repaired by an innate DNA repair mechanism found in cells known as the homology-directed repair pathway. Though therapeutically promising, this method of correcting genes can be inefficient and has other technical challenges.
The authors reasoned that if the microhomology-mediated end joining (MMEJ) pathway could be effectively harnessed, instead of the homology-directed repair pathway, it would remove the duplicated sequence and restore the gene's functional sequence. Less efficient and rarer than other cellular repair mechanisms, the MMEJ pathway often results in deletions on either side of the break and is responsible for performing a small percentage of DNA repairs - less than 10 percent according to some estimates.
The limb-girdle muscular dystrophy type 2G (LGMD2G) caused by a microduplication in the TCAP gene. The scientists treated pluripotent stem cells generated from a LGMD2G patient with a Strepetococcus pyogenesCas9 (SpCas9) nuclease to target a DNA break near the center of the microduplication in the TCAPgene. As they predicted, the MMEJ repair mechanism deleted one copy of the microduplication - effectively stitching the DNA back together again with remarkably high efficiency, leaving out the mutated genetic material and restoring the gene to enable normal TCAP protein to be produced.
"The simplicity and efficiency of microduplication gene editing of the TCAP gene was a very exciting discovery moment, and presented a unique opportunity to develop a therapy for LGMD 2G, which currently is untreatable, and this has become our immediate goal," the author said.
How many diseases are caused by microduplications that might be treated by MMEJ nuclease gene editing? The team demonstrated that microduplications in the HPS1gene associated with Hermanksy-Pudlak syndrome type 1 could be corrected in patient cells. The authors developed computational tools to search human genome databases and remarkably identified 143 diseases associated microduplications that would be treatable using their Cas9-MMEJ approach.
Gene duplications could be fixed with CRISPR/CAS9 and MMEJ repair mechanism
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