01:52pm Wednesday 23 August 2017

CSHL team perfects non-lethal way of switching off essential genes in mice

In a study published on April 12 in the journal Proceedings of the National Academy of Sciences, the scientists demonstrated the feasibility of this approach by turning off a gene necessary for DNA replication in mice until the animals lost weight and were at the brink of death, and then successfully reversing these symptoms and rescuing the mice by turning the gene back on.

The ability to regulate gene activity this way in animals “will not only help in pinpointing timeframes during whichSTILLOWEIn contrast to intestinal cells in normal mice (top), cells in mice in which the RPA3 gene has been shut down by an shRNA fail to proliferate, causing the tissue to atrophy (bottom). essential genes are important during development, but will also be tremendously useful in cancer or other disease-related research,” says CSHL Professor and HHMI investigator Scott Lowe, Ph.D., who co-led the team along with Professor Bruce Stillman, Ph.D., CSHL’s president. “We could, for example, first allow tumors to grow in mice, then shut off a gene that we think might be a good therapeutic target to test whether it saves the animals,” Lowe explains.

To suppress gene activity with RNAi, scientists have been using short hairpin-shaped RNA (shRNA) molecules that attach to matching pieces of the target gene’s RNA and trigger its destruction, thereby shutting down the production of protein from that gene. Having refined and optimized the process of using these shRNA to knock down gene activity in mice over the last few years, Lowe and collaborators including CSHL Professor and HHMI investigator Gregory Hannon, Ph.D., came up with a technology platform, recently published in the journal Cell, that allows them to create genetically modified, or transgenic, mice within 4 months, which is three times faster than standard approaches.

The current study was designed to test whether this new optimized system was robust enough to allow efficient targeting of essential genes. To find the right gene to target, the team first screened an RNAi “library,” or a large collection of shRNAs, to select only molecules that block cell proliferation by shutting off a particular gene. This screening experiment yielded shRNAs against one part—subunit 3—of replication protein A (RPA3), a protein complex discovered in Stillman’s lab in the late 1980s that promotes DNA replication by stabilizing unwinding DNA strands and recruiting other necessary proteins.

The shRNAs that targeted RPA3 were linked to a fluorescent tag. These were then used to generate transgenic mice in such a way that the team could trigger RNAi and shut off the RPA3 gene when the animals were fed a drug like tetracycline but not when the drug was withdrawn. The fluorescent tag allowed the scientists to easily monitor the tissues in which the target RPA3 gene had been switched off.

When the scientists induced RPA3 suppression in adult mice, the animals’ intestinal tissues rapidly atrophied and the mice lost weight and died within 8-11 days. But if the researchers withdrew the drug when the mice were almost at the point of death, both atrophy and weight loss were fully reversed and the mice survived. While the authors plan to further study these mice to understand mechanisms of tissue maintenance and regeneration, they are also excited by the broader implications of their new approach.

“This ability to toggle gene activity at any stage is a major advance over other gene knockdown techniques that are not reversible,” says Stillman. “This approach in animal models is the closest genetic equivalent to treating human patients with a single dose of a small molecule-based therapy targeted at a particular gene. So this system will be invaluable for testing novel therapeutic targets and evaluating their efficacy and side-effects.”


This work was supported by generous gifts from the Don Monti Memorial Research Foundation and a program project grant from the National Institutes of Health.


“Reversible suppression of an essential gene in adult mice using transgenic RNA interference,” appears in online early edition issue of the Proceedings of the National Academy of Sciences in the week of April 11. The full citation is: Katherine McJunkin, Anthony Mazurek, Prem K. Premsrirut, Johannes Zuber, Lukas E. Dow, Janelle Simon, Bruce Stillman, and Scott W. Lowe. The paper can be downloaded at http://www.pnas.org/content/early/2011/04/08/1104097108.full.pdf+html.


About Cold Spring Harbor Laboratory:

Founded in 1890, Cold Spring Harbor Laboratory (CSHL) has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. CSHL is ranked number one in the world by Thomson Reuters for impact of its research in molecular biology and genetics. The Laboratory has been home to eight Nobel Prize winners. Today, CSHL’s multidisciplinary scientific community is more than 400 scientists strong and its Meetings & Courses program hosts more than 8,000 scientists from around the world each year. Tens of thousands more benefit from the research, reviews, and ideas published in journals and books distributed internationally by CSHL Press. The Laboratory’s education arm also includes a graduate school and programs for undergraduates as well as middle and high school students and teachers. CSHL is a private, not-for-profit institution on the north shore of Long Island.

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