DNA低甲基化导致突变率升高
R Z Chen1, U Pettersson, C Beard
1Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA.
Nature
|September 17, 1998
概括
全球DNA低甲基化,癌症的标志,与基因组不稳定性有关. 在小鼠中,DNA甲基转移酶 (Dnmt1) 基因的丢失极大地增加了突变率,突显了DNA甲基化在基因组稳定中的作用.
科学领域:
- 遗传学 是一个遗传学.
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 癌症生物学 癌症生物学
背景情况:
- 全球DNA低甲基化在瘤细胞中观察到,并与基因组不稳定性有关.
- DNA甲基化缺陷可能导致结直肠瘤细胞系不稳定.
- 低甲基化与ICF综合征中的染色体异常以及去甲基化剂有关.
研究的目的:
- 研究DNA甲基化在维持基因组稳定中的作用.
- 为了确定缺乏主要DNA甲基转移酶 (Dnmt1) 的细胞中的突变率.
主要方法:
- 生成的小鼠胚胎干细胞对Dnmt1基因无效.
- 评估了内源性低氨酸基转移酶 (Hprt) 基因和病毒性胺激酶 (tk) 转基因的突变率.
- 分析了突变的类型,包括基因删除,线粒重组和染色体损失.
主要成果:
- 缺少Dnmt1的小鼠胚胎干细胞在Hprt和tk位点都显示出显著增加的突变率.
- 基因缺失是观察到的主要突变类型.
- 线粒体重组或染色体损失与重复是 tk 缺失的主要原因.
结论:
- 哺乳动物DNA甲基化,特别是通过Dnmt1,在维持基因组稳定性方面发挥着至关重要的作用.
- 丢失DNA甲基化可以导致突变率增加和染色体不稳定.
- 这些发现支持了全基因组脱甲基化有助于致癌的假设.
相关概念视频
Mismatch Repair
Overview
Epigenetic Regulation
Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
Overview of DNA Repair
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Chemically...
Epigenetic Regulation
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
X-chromosome...
Mismatch Repair
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...
Spontaneous and Induced Mutations
Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).


