BENGALURU: Furthering research in the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) gene-editing technology that bagged the Nobel Prize in 2020, Indian scientists have demonstrated for the first time that the associated Cas9 enzyme, which acts as molecular scissors to cut DNA at a location specified by a guide
, can bind to and cut the target DNA at very low temperatures.
In their work, scientists from Raman Research Institute (
), Bengaluru, an autonomous institute of the
Department of Science and Technology
), have shown that the highly efficient functioning of this platform at temperatures as low as 4o°C, making it possible to edit genes in temperature sensitive organisms, plants, or crop varieties.
“CRISPR are short DNA sequences found in the genome of prokaryotic organisms such as bacteria, which are reminders of previous bacteriophage (viruses) attacks that the bacteria successfully defended against. Cas9 enzyme (part of bacteria’s defence mechanism) uses these flags to precisely target and cut any foreign DNA, thus protecting the bacteria from future attacks by similar bacteriophages,” the DST explained.
It added that the unprecedented precision of targeting the DNA sequences and then efficiently cutting them is the basis for CRISPR-Cas9 technology, which has been recently demonstrated in editing genes in cells and organisms.
Pointing out that CRISPR-Cas9 technology has been successfully used for many purposes, including basic studies of gene function, agriculture, and medicine to increase our knowledge of disease processes and their potential future therapies, DST said, so far, most binding trials were typically performed at 37 °C.
“As a further step to advance this platform into the forefront of biomedical and analytical biotechnology, RRI scientists have explored temperature-dependent binding and release of cleaved products by the Cas9 enzyme,” DST said.
The research, published in the Scientific Reports journal of the Nature Portfolio, RRI scientists
Serene Rose David
, Divya Shet and
Mahesh B Lakshminarayana
, under the guidance of Gautam V Soni, have demonstrated that the Cas9 enzymes strongly bind to the target at very low temperatures and remains bound to the cleaved DNA products even after the enzyme has done its job.
“...Subsequently, the bound products were released in a controlled fashion using high temperature or chemical denaturant (that make proteins and DNA lose their 3-dimensional structure and become non-functional). The research expands possible application of the Cas9-based genetic toolbox to a previously unexplored temperature range that would be compatible with long-term storage of biological samples,” DST added.
Their observations on high efficiency of Cas9 binding to target at very low temperatures also provide opportunities to edit genomes of the less explored organisms called cryophiles with an optimal growth temperature of 15°C, according to DST.
“The results on Cas9-DNA binding and release mechanics will provide valuable insights for developing temperature-dependent applications of the CRISPR-Cas9 technology. It also builds a quantitative understanding of the product release mechanism of this enzyme system,” DST said.