Illuminating the Inner Workings of Gene Editing
News Jan 25, 2017 | Original story from University of Wisconsin–Madison
Krishanu Saha, right, is working to bring the promise of gene editing technology CRISPR-Cas9 to clinical treatments by watching the editing tool at working inside cells. Photo Courtesy Stephanie Precourt/UW-Madison College of Engineering
University of Wisconsin–Madison engineers have developed methods to observe gene editing in action, and they’re putting those capabilities to work to improve genetic engineering techniques.
“Ultimately, the knowledge we gain from this project has the potential to set the foundation for new preclinical platforms in precision medicine,” says Krishanu Saha, an assistant professor of biomedical engineering at UW–Madison and the principal investigator on the project.
A new technique called CRISPR-Cas9 gives researchers the ability to make changes to the DNA of, theoretically, any living organism that has DNA.
“CRISPR-Cas9 lets researchers rewrite the genome in a very precise manner,” says Saha.
That precision is particularly meaningful for treatment of diseases caused by well-known faults in genes — otherwise incurable diseases such as sickle cell anemia, the fatal lung disorder cystic fibrosis, and the blindness-causing Leber congenital amaurosis. CRISPR-Cas9 could be a way to prevent or reverse those disorders.
But one of the hurdles between CRISPR-Cas9 research and the clinic is that much of what actually happens inside cells while the tool makes its edits has been mysterious.
“There’s been a gap in understanding how several components of CRISPR-Cas9 achieve gene modification in human cells,” says Saha. “Until we understand why some strategies fail and why some succeed, the use of genome surgery tools will be limited.”
With support from a $1.8 million grant from the National Institutes of Health (NIH), Saha could bridge that gap and help pave the way for personalized treatment for genetic diseases.
His lab has already found one method to illuminate the inner workings of gene editing, developing a way to label parts of cells and CRISPR-Cas9 in such a manner that they may observe important changes occurring while genome-editing happens in real time. The researchers will use those techniques to monitor CRISPR-Cas9 as it works inside cells in petri dishes that mimic tissues from real patients. Drawing on their expertise with stem cells to make model organs in which to test different genome-editing strategies, Saha and collaborators will investigate multiple approaches to correcting the problems for several genetic diseases in numerous different types of tissues.
“This project is different from the status quo,” says Saha. “Systematically changing multiple components of CRISPR-Cas9 at a time to test in patient-derived cells will lead to greater understanding of the biological processes important for genome surgery.”
Saha’s work is supported by a relatively new type of grant from NIH, the Maximizing Investigators’ Research Award, that aims to boost scientific productivity and innovation by providing both greater stability in funding and more freedom to pursue revolutionary research. Saha is one of 93 promising young investigators nationwide identified for the transformative potential of his work.
This article has been republished from materials provided by University of Wisconsin–Madison. Note: material may have been edited for length and content. For further information, please contact the cited source.
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