Crispr-based gene repression is a powerful tool used in molecular biology to selectively inhibit gene expression. This technique utilizes a modified version of the CRISPR-Cas9 system, where the Cas9 protein is deactivated (often referred to as dCas9) and fused with a repressor domain. When targeted to specific DNA sequences by a guide RNA, dCas9 binds to the DNA but does not cut it, effectively blocking the transcription machinery from accessing the gene. This process can lead to efficient silencing of unwanted genes, which is particularly useful in research, therapeutic applications, and biotechnology. The versatility of this system allows for the simultaneous repression of multiple genes, enabling complex genetic studies and potential treatments for diseases caused by gene overexpression.
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