DREAM tool for gene therapies uses ‘locally sourced’ components | Rice News | News and Media Relations
Sourcing some materials closer to home may be a good practice not only in the produce aisle but also the synthetic biology lab.
Seeking to minimize the use of components derived from viral sources, Rice University bioengineers developed a tool that activates silent or insufficiently expressed genes using human-derived proteins known as mechanosensitive transcription factors that naturally enable our cells to turn on specific genes in response to mechanical cues.
Dubbed CRISPR-DREAM (for CRISPR-dCas9 recruited enhanced activation module or DREAM for short), the tool is smaller, more effective and less toxic to medically useful cell types than other state-of-the-art technologies used to control gene expression, according to a study published in Nature Methods.
The DREAM tool could enable better and safer gene and cell therapies and more accurate disease models to address haploinsufficiency disorders, which cause a number of hard-to-treat conditions such as epilepsy and some forms of cancer, immunodeficiency and Alzheimer’s disease.
“Many human diseases are driven by problems with too little of a gene being produced,” said Isaac Hilton, assistant professor of bioengineering and biosciences at Rice. “You encounter these health issues where people don’t make enough of a certain protein or gene product, and in those cases, unfortunately there are often few therapeutic options.”
To address this issue, in recent years researchers have used CRISPR-based targeting systems to develop cutting-edge synthetic transcription factors. Most of these tools are built with materials of nonhuman origin, which may come with unwanted side effects.
“One challenge with some of the current technologies is that they are built using viral proteins that have evolved to reprogram how our cells work, and they do so in ways that are of course not necessarily beneficial,” Hilton said. “And even though virally derived elements can be engineered to work for the host cell’s benefit, we and others have observed in our research that they can still cause some toxicity in human cells.”
Instead of relying on virally derived proteins, Barun Mahata, a postdoctoral researcher in Hilton’s lab, sought to employ transcription factors that human cells already make and use. Mahata fused the specific parts of these proteins responsible for activating genes to CRISPR-based programmable delivery platforms using a method intended to enhance their transcriptional powers.
“We harnessed the natural ability of human-derived transcription factors, or proteins responsible for gene synthesis in the cells of our body,” said Mahata, who is the lead author on the study. “The transcription activation units we built function in a very precise way. They induce gene activity where we target them and can activate very rapid and robust transcription.”
They also help tackle another disadvantage of current synthetic gene-activation platforms, which are often too large for efficient delivery to human cells.
“What we did was look for small segments of human proteins that we could leverage to apply these technologies in human cells more effectively,” said Hilton, the corresponding author on the study and a Cancer Prevention and Research Institute of Texas (CPRIT) scholar. “When we started this project of building synthetic transcription factors with human-derived proteins, we wanted to identify the ideal source material with compactness being one key factor.”
Human mechanosensitive transcription factors ⎯ proteins that our cells and organs use to respond to mechanical forces ⎯ met the researchers’ criteria: In addition to being relatively small, they are quick-acting and widely used by nearly all human cell types.
Moreover, the team was able to activate up to 16 different locations on the genome simultaneously ⎯ a record number for synthetic transcription factors.
“The reason why that capability is particularly important is because when our cells perform a function, it’s not just that they turn on a single gene,” Hilton said. “Instead, they typically turn on whole constellations or networks of genes in concert. And we can now use these synthetic transcription factors to mimic and engineer what our cells do naturally.”
The researchers showed that the DREAM tool could be used to convert skin cells to induced pluripotent stem cells (iPSCs) in a dish as a proof of concept exercise ⎯ a feat that Hilton says carries “tremendous biomedical utility” in the long run.
The research was supported by the Cancer Prevention and Research Institute of Texas (RR170030), the National Institutes of Health (R35GM143532, R21EB030772, R56HG012206), the American Heart Association (917025), the Fulbright Program, the National Council of Science and Technology of Mexico and the National Science Foundation.
- Peer-reviewed research:
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“Compact engineered human mechanosensitive transactivation modules enable potent and versatile synthetic transcriptional control” | Nature Methods | DOI: 10.1038/s41592-023-02036-1
Authors: Barun Mahata, Alan Cabrera, Daniel Brenner, Rosa Selenia Guerra-Resendez, Jing Li, Jacob Goell, Kaiyuan Wang, Yannie Guo, Mario Escobar, Abinand Krishna Parthasarathy, Hailey Szadowski, Guy Bedford, Daniel Reed, Sunghwan Kim and Isaac B. Hilton
- Image downloads:
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CAPTION: Isaac Hilton (right) is an assistant professor of bioengineering and biosciences and CPRIT scholar; Barun Mahata (left) is a postdoctoral researcher in Hilton’s lab at Rice University. (Photo courtesy of Hilton lab/Amaury F. Bittar Yepes)
CAPTION: The CRISPR-DREAM platform enables new opportunities for synthetic biology and gene and cell therapies such as 1) reprogramming specialized cells (e.g., skin cells) into induced pluripotent stem cells; 2) streamlining gene therapy vectors to activate genes in clinical contexts; 3) activating insufficiently expressed genes to help treat different diseases; and 4) restoring the immunoprotective function of malfunctioning T-cells. (Image courtesy of the Hilton lab/Rice University)
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- Links:
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Hilton lab:
Cancer Prevention and Research Institute of Texas: https://www.cprit.state.tx.us/
Department of Bioengineering:
George R. Brown School of Engineering:
- About Rice:
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Located on a 300-acre forested campus in Houston, Rice University is consistently ranked among the nation’s top 20 universities by U.S. News & World Report. Rice has highly respected schools of Architecture, Business, Continuing Studies, Engineering, Humanities, Music, Natural Sciences and Social Sciences and is home to the Baker Institute for Public Policy. With 4,552 undergraduates and 3,998 graduate students, Rice’s undergraduate student-to-faculty ratio is just under 6-to-1. Its residential college system builds close-knit communities and lifelong friendships, just one reason why Rice is ranked No. 1 for lots of race/class interaction and No. 4 for quality of life by the Princeton Review. Rice is also rated as a best value among private universities by Kiplinger’s Personal Finance.
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