相关实验视频
Updated: Jun 29, 2025

08:50
A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
2.6K
核酸脱胺酶:基编辑工具包中的关键参与者
Jiangchao Xiang1, Wenchao Xu1, Jing Wu1
1Gene Editing Center, School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Biophysics reports
|March 25, 2024
概括
核酸脱氨酶通过催化特定基因变化,使精确的基因编辑成为可能. 工程和发现新的deaminases提高基础编辑器的效率和特异性,用于更广泛的应用.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
- 基因编辑技术的技术
背景情况:
- 基数编辑器使用核酸脱氨酶进行针对性的单基数修改.
- 氨酸和氨酸脱氨酶分别调解氨酸到氨酸 (A-to-I) 和氨酸到尿素 (C-to-U) 的转化.
- 这些酶对于精确的遗传改变至关重要.
研究的目的:
- 审查当前关于在基础编辑中使用的除氨酶的知识.
- 为了突出酶工程和发现的进步.
- 讨论对基础编辑器应用程序和特异性的影响.
主要方法:
- 在基础编辑中对核酸脱氨酶的现有文献的审查.
- 对结构特征和催化机制的分析.
- 检查酶优化和进化策略的研究.
主要成果:
- 工程和新型核酸脱氨酶显著改善了基数编辑.
- 增强的酶提供更广泛的应用范围和更高的编辑特异性.
- 了解酶结构和机制是优化关键.
结论:
- 核酸脱氨酶对于基编辑的精度和效率至关重要.
- 在酶工程和发现领域的持续研究继续扩大基编辑技术的潜力.
- 未来的方向涉及进一步优化,以提高特异性和更广泛的治疗应用.
相关概念视频
RNA Editing
9.0K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.0K
Base Excision Repair
22.3K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
The first step of...
22.3K
Proofreading
54.1K
Overview
54.1K
DNA Base Pairing
27.4K
Erwin Chargaff’s rules on DNA equivalence paved the way for the discovery of base pairing in DNA. Chargaff’s rules state that in a double-stranded DNA molecule,
27.4K
Long-patch Base Excision Repair
7.0K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
7.0K
Mismatch Repair
4.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
4.8K

