Genetic eraser: Newly developed technology precisely and rapidly degrades targeted proteins

Genetic eraser: Newly developed technology precisely and rapidly degrades targeted proteins
A degron-fused protein of interest is recognized for rapid degradation by a TIR1 mutant only in the presence of an auxin analog, which initiates the degradation process. The target protein is typically depleted in less than a few hours after treatment. Credit: Masato Kanemaki

Researchers can now more accurately and precisely target specific proteins in yeast, mammalian cells and mice to study how knocking down specific protein traits can influence physical manifestation in a cell or organism.

The Japan-based team published their results on November 11th in Nature Communications.

"Conditional gene knockout and small interfering RNA (siRNA), which is used to silence proteins without knocking them out completely, has been employed in many studies," said Masato T. Kanemaki, professor at the National Institute of Genetics in the Research Organization of Information and Systems (ROIS). "However, these technologies are not ideal for studying highly dynamic processes, such as , differentiation or , because of the slow rate of depletion of the of interest."

Kanemaki and his team had previously developed an approach called the AID system, which uses a small protein tag, known as a degron, fused to proteins to induce . To initiate the degradation process, the researchers administered auxin, a plant hormone that helps regulate plant growth. In previous conditional gene knockout and siRNA studies, according to Kanemaki, it typically takes two or three days for a target protein to deplete. The AID system allows for a general, more efficient approach by which the can be depleted in less than a few hours.

"The original AID system has two major drawbacks: leaky degradation and the requirement for a high dose of auxin," Kanemaki said. "These make it difficult to control precisely the expression level of a protein of interest in living and apply this method to mice."

The ability to knock out genes in mice is a critical step in genetic research and therapeutics. According to Kanemaki, an approach may work well in cultured cells, but it must work in a whole model system, such as a mouse. The "leaky degradation" of the AID system meant that a targeted protein would only degraded weakly without auxin, but the level of auxin required to induce full degradation appeared to have long-term negative effects on cell growth.

"In this paper, we describe the AID2 system, which overcomes all the drawbacks of the original AID system," Kanemaki said, noting that they did not detect leaky degradation with the system, the degradation was quicker, and the required dose of auxin was much lower.

To establish the AID2 system, the researchers employed what is known as a "bump-and-hole" strategy to create an empty space in a mutant version of a plant protein (called TIR1) that recognizes and induces the degradation of degron-fused proteins. An auxin analog can bind directly to the TIR1 mutant and initiate the . Since the approach is very efficient, less auxin analog is needed. The researchers found that depletion could be induced at a concentration about 670 times lower than in the original system.

"With the AID 2 system, it is possible to rapidly deplete a protein of interest in cultured cells and mice," Kanemaki said. "Next, we plan to use the system to find something new in chromosome biology, and to apply the AID2 system to other model organisms."


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More information: Aisha Yesbolatova et al. The auxin-inducible degron 2 technology provides sharp degradation control in yeast, mammalian cells, and mice, Nature Communications (2020). DOI: 10.1038/s41467-020-19532-z
Journal information: Nature Communications

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Citation: Genetic eraser: Newly developed technology precisely and rapidly degrades targeted proteins (2020, November 11) retrieved 27 July 2021 from https://phys.org/news/2020-11-genetic-eraser-newly-technology-precisely.html
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