庇护素成分TRF2调解了人类端粒染色素的柱状堆叠
Sook Yi Wong1,2, Aghil Soman1, Nikolay Korolev1
1School of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore.
The EMBO journal
|January 4, 2024
概括
端粒重复结合因子2 (TRF2) 稳定了端粒色素纤维,促进了柱状结构. 这种结合增强了这些关键DNA结构的机械和热力学稳定性.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 生物物理学的生物物理.
背景情况:
- 端粒重复结合因子2 (TRF2) 对端粒功能和非端粒过程至关重要.
- 了解TRF2与端粒核细胞的相互作用是有限的.
研究的目的:
- 为了研究TRF2与体外复合的人类端粒染色素纤维的结合.
- 阐明TRF2结合的结构和机械后果.
主要方法:
- 电子显微镜 (EM) 用于结构分析.
- 单分子力光谱学 (SMFS) 使用磁子进行机械稳定.
- 分析超离心沉速度 (AUC-SV). 分析超离心沉速度 (AUC-SV). 分析超离心沉速度 (AUC-SV). 分析超离心沉速度 (AUC-SV). 分析超离心沉速度 (AUC-SV). 分析超离心沉速度 (AUC-SV).
主要成果:
- 结合TRF2促进端粒纤维中的柱状结构,增加宽度和紧.
- SMFS发现,TRF2显著提高了端粒纤维的机械和热力学稳定性.
- 与"Widom 601"序列相比,TRF2的稳定作用在端粒序列上更为明显.
结论:
- 结合TRF2诱导和稳定柱状端粒染色素纤维.
- 这些稳定结构可能对有效的端粒维护至关重要.
- TRF2在组织和稳定端粒染色质中发挥着关键作用.
更多相关视频
09:13Generation of Cancer Cell Clones to Visualize Telomeric Repeat-containing RNA TERRA Expressed from a Single Telomere in Living Cells
Published on: January 17, 2019
7.4K
09:26Isolation of Specific Genomic Regions and Identification of Associated Molecules by enChIP
Published on: January 20, 2016
10.5K
相关概念视频
Telomeres and Telomerase
23.4K
In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded...
23.4K
Replicative Cell Senescence
3.6K
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds...
3.6K
Replication in Eukaryotes
13.8K
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
13.8K
Spreading of Chromatin Modifications
8.3K
The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
Writers
The writer...
8.3K
Nucleosome Remodeling
9.1K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
9.1K
Restarting Stalled Replication Forks
5.8K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
5.8K
