最近在基于CRISPR的功能基因组学方面取得的进展,用于研究与疾病相关的遗传变异
Heon Seok Kim1,2,3, Jiyeon Kweon4, Yongsub Kim5,6
1Department of Life Science, College of Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Experimental & molecular medicine
|March 31, 2024
概括
通过精确编辑DNA,CRISPR-Cas系统和测序工具可以实现功能性基因组学. 这种方法有助于理解基因突变,将不确定的数据转化为精准医学的可操作的见解.
科学领域:
- 基因组学就是基因组学.
- 分子生物学分子生物学
- 生物技术是生物技术.
背景情况:
- 基因组数据的生成已经激增,但解释含义不明的遗传变异 (VUSs) 是精准医学中的一个挑战.
- 了解基因突变的功能影响对于推进个性化医疗保健至关重要.
研究的目的:
- 审查CRISPR-Cas系统和功能基因组学测序工具组合.
- 要突出它们在特征点突变和VUSs中的应用.
主要方法:
- CRISPR-Cas系统用于精确的基因组工程和VUS整合.
- 整合CRISPR-Cas技术与测序,用于高通量突变评估.
主要成果:
- 克里斯普尔-Cas使得功能研究的基因变异能够有针对性地引入.
- 结合方法促进对突变影响的高通量分析.
- 允许对点突变后果进行全面研究.
结论:
- CRISPR-Cas和测序工具正在改变功能基因组学.
- 这些技术将不确定的遗传数据转化为精准医学的可操作见解.
- 有助于更深入地了解遗传突变效应.
相关概念视频
CRISPR
50.8K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
50.8K
Genome-wide Association Studies-GWAS
13.4K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
13.4K
Homologous Recombination
50.5K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.5K
Single Nucleotide Polymorphisms-SNPs
15.0K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.0K
CRISPR and crRNAs
17.0K
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
17.0K
What is Genetic Engineering?
74.1K
Overview
74.1K


