微核中的DNA和染色质的细胞内和细胞外命运决定了它们的致病性
Micheline Kirsch-Volders1, Michael Fenech2, Miroslav Mišík3
1Laboratory for Cell Genetics, Department Biology, Faculty of Sciences and Bio-engineering Sciences, Vrije Universiteit Brussel, Pleinlaan 2, Brussels 1050, Belgium.
Mutation research. Reviews in mutation research
|September 3, 2025
概括
微核 (MN) 和它们的DNA是基因组不稳定性和炎症的关键因素. 在循环无细胞DNA (cfDNA) 中的MN衍生DNA可能为疾病诊断和监测提供新的见解.
科学领域:
- 基因组学
- 分子生物学
- 生物标志物发现
背景情况:
- 循环无细胞DNA (cfDNA) 是一种重要的非侵入性生物标志物,用于疾病管理.
- 细胞质DNA有助于基因不稳定和炎症,
- 细胞内和细胞外DNA的复杂性带来了分析挑战.
研究的目的:
- 审查微核 (MN) 和它们的DNA的起源,组成和命运.
- 突出MN在基因组不稳定性和免疫激活中的作用.
- 探索MN衍生DNA对cfDNA生物标志物的影响.
主要方法:
- 综合了目前的MN生物学证据.
- 检查MN形成,细胞内结果和膜破裂.
- 探索MN挤出机制及其对cfDNA的影响.
主要成果:
- 微核 (MN) 是由染色体片段或整个染色体形成的.
- MN破裂可能导致染色体和cGAS-STING介导的炎症.
- 可以挤出MN或它们的DNA,从而影响cfDNA的组成和检测.
结论:
- 源自MN的DNA和染色体与基因组不稳定性和疾病进展有关.
- MN生物学提供了关于cfDNA组成和生物标志物潜力的见解.
- 需要对MN清除,组织来源和血检测性进行进一步的研究.
相关概念视频
Chromatin Position Affects Gene Expression
23.7K
Chromatin is the massive complex of DNA and proteins packaged inside the nucleus. The complexity of chromatin folding and how it is packaged inside the nucleus greatly influences access to genetic information. Generally, the nucleus' periphery is considered transcriptionally repressive, while the cell's interior is considered a transcriptionally active area.
Topologically Associated Domains (TADs)
The 3-dimensional positioning of chromatin in the nucleus influences the...
Topologically Associated Domains (TADs)
The 3-dimensional positioning of chromatin in the nucleus influences the...
23.7K
Mutagenicity and Carcinogenicity
1.4K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.4K
Inheritance of Chromatin Structures
6.6K
Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
6.6K
Chromatin Packaging
16.0K
Each human somatic cell contains 6 billion base-pairs of DNA. Each base-pair is 0.34 nm long, which means that each diploid cell contains a staggering 2 meters of DNA. How is such a long DNA strand packed inside a nucleus measuring only 10 - 20 microns in diameter?
The chromatin
In combination with specialized DNA binding protein called Histones, the DNA double helix forms a compact DNA: protein complex called chromatin. The chromatin itself is further compacted into higher-order...
The chromatin
In combination with specialized DNA binding protein called Histones, the DNA double helix forms a compact DNA: protein complex called chromatin. The chromatin itself is further compacted into higher-order...
16.0K
Nucleotide Excision Repair
3.8K
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.8K
Mutations
39.7K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
39.7K


