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相关概念视频

Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

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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:
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Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
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Mismatch Repair01:36

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RNA Splicing01:32

RNA Splicing

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Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
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Nucleotide Excision Repair01:08

Nucleotide Excision Repair

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Base Excision Repair01:54

Base Excision Repair

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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...
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相关实验视频

Updated: Jun 26, 2025

Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
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(G) 在癌症中修复错误拼接.

Maciej Cieśla1, Cristian Bellodi2

  • 1IMol Polish Academy of Sciences, Warsaw, Poland.

Trends in biochemical sciences
|May 18, 2024
PubMed
概括

G补丁基因蛋白GPATCH8对于剪接因子SF3B1.1.的致癌突变至关重要. 向GPATCH8为SF3B1突变癌症和拼接相关疾病提供了新的治疗策略.

科学领域:

  • 分子生物学分子生物学
  • 癌症遗传学 癌症遗传学
  • 在RNA分离过程中.

背景情况:

  • 剪接因子SF3B1的突变在各种癌症中很常见.
  • 异常RNA拼接有助于癌症的发展和进展.

研究的目的:

  • 研究GPATCH8在SF3B1突变癌症中的作用.
  • 探索GPATCH8作为一个潜在的治疗目标.

主要方法:

  • 利用分子生物学技术研究蛋白质相互作用.
  • 在具有SF3B1突变的癌症细胞系中分析了拼接模式.

主要成果:

  • GPATCH8与突变型SF3B1合作,导致异常拼接.
  • 在SF3B1-突变癌症中,GPATCH8对于错误拼接表型至关重要.

结论:

  • 在SF3B1突变癌症的发病过程中,GPATCH8发挥着至关重要的作用.
  • 针对GPATCH8为这些癌症和其他与拼接相关的疾病提供了一个有希望的治疗途径.
关键词:
DHX15 DHX15 的时间.G-补丁域名域名在GPATCH8中使用.在SF3B1中.在 SUGP1 中,拼接 拼接 拼接 拼接

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