“This technique allows us to avoid bombarding cells with various growth factors and gene activators and repressors to get them to differentiate,” Levy said. They were also able to show they could transdifferentiate induced pluripotent stem cells to placental progenitor cells by simply turning on two genes. In the new paper, Levy and her colleagues show that by using this technique, they were able to block PRC2 and selectively turn on four different genes. The guide RNA is like a passenger, telling the UBER where to go.” “dCas9 is like UBER,” says Levy, “It will take you anywhere on the genome you want to go. The AI-designed blocking protein was the cargo of the dCas9-RNA construct. As a result, it’s called dCas9, for “dead.” However, the Cas9 function as a “vehicle” to deliver cargo to a specific location remains active. In this experiment, however, the cutting function of the Cas9 protein is disabled so the genomic DNA sequence is unaltered. The system allows scientists, by synthesizing a specific “address-tag” RNA, to bring Cas9 to a precise location in genome and therefore cut and splice genes at specific sites. Cas9 binds and uses RNA as an address-tag. Ruohola-Baker and Levy then fused this designed protein with a disabled version of a protein called Cas9.Ĭas9 is the protein used in the gene editing process called CRISPR. To do this, David Baker and his colleagues use AI to create a protein that would bind to PRC2 and block a protein the PRC2 uses to modify the histones. The goal of the UW researchers was to find a way to block PRC2 so that only one gene at a time would be affected. PRC2 is active throughout development but plays a particularly important role during the first days of life when embryonic cells differentiate into the variouscell types that will form the tissues and organs of the growing embryo. PRC2 can be blocked with chemicals, but they are imprecise, affecting PRC2 function throughout the genome. These methyl groups must be refreshed so if PRC2 is blocked the genes it has silenced. In their work, Levy and her colleagues focused on a complex of proteins called PRC2 that silences genes by attaching a small molecule, called a methyl group, to a protein that packages genes called histones. Scientists are particularly interested in epigenetic modifications because not only do they affect gene activity in normal cell function, epigenetic markers accumulate with time, contribute to aging, and can affect of the health of future generations as we can pass them on to our children. The chemical modifications that regulate gene activity are called epigenetic markers. Because these modifications occur not in, but on top of genes, they are called epigenetic, from the Greek epi “over” or “above” the genes. The new technique controls gene activity without altering the DNA sequence of the genome by targeting chemical modifications that help package genes in our chromosomes and regulate their activity. The AI-designed protein was developed at the UW Medicine Institute for Protein Design (IPD) under the leadership of David Baker, also a professor of biochemistry and head of the IPD. The project was led by Hannele Ruohola-Baker, professor of biochemistry and associate director of ISCRM. “The beauty of this approach is we can safely upregulate specific genes to affect cell activity without permanently changing the genome and cause unintended mistakes,” Levy said. The approach will allow researchers to understand the role individual genes play in normal cell growth and development, in aging, and in such diseases as cancer, said Shiri Levy, a postdoctoral fellow in UW Institute for Stem Cell and Regenerative Medicine (ISCRM) and the lead author of the paper. Researchers from the University of Washington School of Medicine in Seattle describe this finding in the journal Cell Reports. By combining CRISPR technology with a protein designed with artificial intelligence, it is possible to awaken individual dormant genes by disabling the chemical “off switches” that silence them.
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