Research groups at Kinki University, Kitasato University, and Tokyo Institute of Technology have succeeded for the first time in the world in "writing" DNA methylation in fertilized mouse eggs using "epigenome editing technology."
All the cells that make up the human body have the same genetic information (genome) in the nucleus.Various tissues and cells are created from this same genetic information because the genes required for each cell are used and unnecessary genes are not used.
Epigenome is called acquired genetic information and is a general term for information other than DNA base sequences that are inherited even after mitosis.One of the epigenomes is DNA methylation, which is said to play an important role in normal ontogeny.In addition, epigenome editing is an application of "genome editing" technology used for genetic recombination.It is a technology that can manipulate the DNA methylation state of a specific gene region and change the marker required for reading genetic information.
In this research, we succeeded in writing DNA methylation information to fertilized mouse eggs using epigenome editing technology and enzyme genes derived from bacteria, and it is possible to efficiently introduce DNA methylation into fertilized eggs. showed that.
DNA methylation operations are expected to contribute to cancer research in the future.It has been reported that DNA demethylation of centromeres (chromosomal sequences essential for cell division) occurs on a large scale in mouse germ cells and multiple cancer cells. DNA methylation manipulation technology is said to enable the study of the causal relationship between genomic instability and DNA hypomethylation status in cancer cells.
Also, unlike genome editing used for gene recombination, epigenome editing can suppress gene expression without gene disruption.Therefore, it is expected to be applied to gene therapy that does not rewrite the genome, such as suppressing the expression of disease-causing genes without causing ethical problems.
Paper Information: [PLOS ONE] Targeted DNA Methylation in Pericentromeres with Genome Editing-Based Artificial DNA Methyltransferase.