Controlling Gene Expression in Stem Cells
News Mar 14, 2016
The development offers a major technological advance in creating cell models of genetic diseases.
The researchers used a modified version of CRISPR called CRISPR interference (CRISPRi) to inactivate genes in iPSCs and heart cells created from iPSCs. The method, first reported in 2013by Stanley Qi, PhD, a co-author on the current paper, significantly improves the original CRISPR-Cas9 system by allowing genes to be silenced—or turned off—more precisely and efficiently. CRISPRi also offers the flexibility of reversing and carefully controlling the amount of gene suppression.
The standard CRISPR system uses the protein Cas9 to delete a precise part of the genome by making small cuts in a cell’s DNA. CRISPRi builds on this technology by using a special deactivated version of the Cas9 protein and an additional inhibitor protein, KRAB. Together, these proteins sit at the target spot on the genome and suppress gene expression without cutting the DNA. To the scientists’ surprise, temporarily silencing gene expression in this way was much more consistent than permanently cleaving the genome.
“We were amazed by the dramatic difference in performance between the two systems,” said senior author Bruce Conklin, MD, a senior investigator in the Gladstone Institute of Cardiovascular Disease and Roddenberry Stem Cell Center at Gladstone. “We thought that permanently cutting the genome would be the more effective way to silence a gene, but in fact, CRISPRi is so precise and binds so tightly to the genome that it is actually a better way to silence a gene.”
In the study, the researchers compared how well CRISPRi and CRISPR-Cas9 silenced a particular gene that controls iPSC pluripotency—the capability of iPSCs to turn into multiple cell types. They discovered that CRISPRi was much more efficient than CRISPR-Cas9: in more than 95% of the cells created using CRISPRi, the target gene was silenced, compared with only 60-70% of cells grown from CRISPR-Cas9. CRISPRi also did not cause any off-target changes in gene expression, like undesired insertions or deletions to the cell’s genome, which is a concern with CRISPR-Cas9.
CRISPRi also acted like a toggle switch, enabling the scientists to reverse gene suppression by simply removing the chemical that turns on the gene inhibitor. In addition, the researchers were able to tune how much they silenced a gene by changing the amount of the chemicals they added. Both of these results support much more versatile investigations into the role of certain genes that affect development and disease.
The researchers demonstrated the enhanced capabilities of CRISPRi in iPSCs, T cells, and heart cells made from stem cells. For example, they created a model of heart disease using genome editing to suppress a gene essential for heart function.
“CRISPRi holds a major advantage in making disease-relevant cell types,” said first author Mohammad Mandegar, DPhil, a research scientist at Gladstone. “Using this technology, we can mimic disease in a homogenous population of heart cells created from iPSCs. This development allows us to study genetic diseases more easily and potentially identify new therapeutic targets.”
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