Nature: CRISPR single base editing is accurate

Researchers from the Korea Institute of Basic Science, IBS, published an article entitled "Genome-wide target specificities of CRISPR RNA-guided programmable deaminases", confirming the accuracy of recently developed genetic editing methods. The research was published in the April 10 issue of Nature Biotechnology.

The author of the article is KIM Jin-Soo, a big man in the field of genetic editing. His research group has published many articles in top journals such as Nature, and put forward many innovative ideas in the field of CRISPR technology. For example, they have designed the smallest ones. CRISPR-Cas9, which is delivered to the eyes of muscle cells and mice by adeno-associated virus (AAV) to edit the genes that cause blindness.

Nature:CRISPR单碱基编辑准确

For the latest study, Kim said, "This is the first time that the accuracy of this base editing has been verified at the entire genome level."

The rapid development of gene editing tools has made the whole biological research field crazy. The main character of the third generation DNA scissors is CRISPR, which is a faster and cheaper tool than its predecessor. CRISPR-Cas9 and CRISPR-Cpf1 silence or reduce the expression of erroneous genes by excising small DNA sequences. However, last year's new method of base editing: instead of causing random DNA deletions and insertions, it replaced a DNA gene and attracted the attention of biologists.

This method of genetic correction is critical because some diseases are caused by errors in one of the four basic components of DNA (adenine (A), cytosine (C), guanine (G), and thymine (T)). . Single nucleotide errors in DNA are called point mutations, and diseases caused by point mutations include cystic fibrosis, sickle cell anemia, and color blindness.

Unlike the existing third-generation DNA scissors, the single-base editing method consists of a variant of CRISPR-Cas9 (nCas9, nickase) and another called cytosine deaminase, replaced by T. C, directing the correct DNA position by targeting RNA. But so far, it is not known whether this base editor works only in the wrong gene region, or can be replaced (off-target) in other regions.

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