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 이성욱 ( 2017-07-02 11:24:33 , Hit : 1127
 CRISPR Platform Scans DNA to Predict Off-Target Effects

http://www.genengnews.com/gen-news-highlights/crispr-platform-scans-dna-to-predict-off-target-effects/81254601?utm_medium=newsletter&utm_source=GEN+Daily+News+Highlights&utm_content=01&utm_campaign=GEN+Daily+News+Highlights_20170630


GEN News Highlights
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June 30, 2017

  
The heart of the new technique for detecting interactions between CRISPR and off-target DNA segments is a standard next-generation gene-sequencing slide (also known as flow cell), produced by Illumina. [Wikimedia user Bainscou, via Creative Commons Attribution 3.0 license]


If you’re reworking a genome, you might want to heed the old saying, “Measure twice, cut once.” Otherwise, your attempts to right the genome or modify it for special purposes could end in genomic wrongs—off-target effects. For example, the popular gene-editing tool known as CRISPR could go astray, altering genes other than the ones it was meant to alter. If only CRISPR’s potential slips could be foreseen! Then, perhaps, they could be avoided, and CRISPR would realize its potential not only in research, but also in medicine.

Scientists from The University of Texas at Austin took an important step toward safer gene-editing cures for life-threatening disorders, from cancer to HIV to Huntington's disease, by developing CHAMP, which stands for chip-hybridized association-mapping platform. It repurposes next-generation sequencing chips to enable the massively parallel profiling of protein–nucleic acid interactions.

The scientists used CHAMP to provide the first comprehensive survey of DNA recognition by a type I-E CRISPR-Cas (Cascade) complex and Cas3 nuclease. CHAMP, the scientists showed, was able to simultaneously measure the interactions between proteins and ∼107 unique DNA sequences.

Additional details appeared June 29 in the journal Cell, in an article entitled, “Massively Parallel Biophysical Analysis of CRISPR-Cas Complexes on Next Generation Sequencing Chips.” These details suggest that CHAMP provides a framework for high-throughput, quantitative analysis of protein–DNA interactions on synthetic and genomic DNA.

“Analysis of mutated target sequences and human genomic DNA reveal that Cascade recognizes an extended protospacer adjacent motif (PAM),” the article’s authors wrote. “Cascade recognizes DNA with a surprising 3-nt [nucleotide] periodicity. The identity of the PAM and the PAM-proximal nucleotides control Cas3 recruitment by releasing the Cse1 subunit.”

Essentially, these findings led to a model for the biophysical constraints governing off-target DNA binding. This model, for example, suggests that Cascade pays less attention to every third letter in a DNA sequence than to the others.

"So, if it were looking for the word 'shirt' and instead found the word 'short,' it might be fine with that," explained Stephen Jones, Ph.D., a postdoctoral researcher at UT Austin and one of three co-lead authors of the Cell paper.

Knowing such rules could lead to better computer models for predicting which DNA segments a specific CRISPR molecule is likely to interact with. And that can save time and money in developing personalized gene therapies.

"You and I differ in about 1 million spots in our genetic code," said Ilya Finkelstein, Ph.D., an assistant professor in the department of molecular biosciences at UT Austin and the project's principal investigator. "Because of this genetic diversity, human gene editing will always be a custom-tailored therapy."

The researchers took a DIY approach to developing the equipment and software for their technique, using existing laboratory technology. The heart of the test is a standard next-generation genome sequencing chip already widely used in research and medicine. Two other key elements—designs for a 3D printed mount that holds the chip under a microscope and software the team developed for analyzing the results—are open source. As a result, other researchers can easily replicate the technique in experiments involving CRISPR.

"Next-generation genome sequencing was invented to read genomes, but here we've turned the technology on its head to allow us to characterize how CRISPR interacts with genomes," noted Andy Ellington, Ph.D., a professor in the department of molecular biosciences, vp for research of the Applied Research Laboratories at UT Austin, and a co-author of the paper.

"If we're going to use CRISPR to improve peoples' health, we need to make sure we minimize collateral damage,” commented Dr. Jones. “And this work shows a way to do that."







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