平衡行为:BRCA2通过控制G-四重复的动态性来精心管理端粒复制
So Young Joo1, Keewon Sung2, Hyunsook Lee1
1Department of Biological Sciences & Institute of Molecular Biology and Genetics (IMBG), Seoul National University, Seoul, South Korea.
概括
端粒G四复合体 (G4) 在形状之间动态切换. 瘤抑制剂BRCA2与G4中间体相互作用,帮助复制叉重新启动并保持端粒稳定性.
科学领域:
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
- 生物化学 生化学
背景情况:
- 类真核生物保留具有富含关氨酸的重复的端粒,形成G-四重复 (G4) 结构.
- 端粒G4结构的进化意义仍然不清楚.
研究的目的:
- 为了研究端粒G4结构的动态性质.
- 阐明BRCA2与端粒G4之间的相互作用.
- 了解G4动态在端粒复制中的作用.
主要方法:
- 对G4形状动态的观测研究.
- 对BRCA2-G4相互作用的分析.
- 复制叉重新启动试验.复制叉重启试验.
主要成果:
- 端粒G4结构在至少两个不同的形状之间振荡.
- 在G4状态过渡期间,BRCA2直接与G-三倍体中间体相互作用.
- 结合BRCA2促进G4重塑,并促进复制叉重新启动.
结论:
- 端粒G4动态对于维持复制恒常状态至关重要.
- 在解决阻碍复制的G4结构方面,BRCA2发挥着关键作用.
- 失去G4动态可以导致端粒复制受损和潜在的基因组不稳定.
关键词:
这就是BRCA2的原因.G-四重复式 (G4) 是一个G四重复式.在R-loop中使用R-loop.在地球上,地球是地球.复制分叉拖延时间 拖延时间复制重新启动复制.端粒是什么意思 端粒是什么意思更多相关视频
08:53Identifying the Effects of BRCA1 Mutations on Homologous Recombination using Cells that Express Endogenous Wild-type BRCA1
Published on: February 17, 2011
14.6K
08:31Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy
Published on: June 8, 2018
9.1K
相关概念视频
Telomeres and Telomerase
23.3K
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...
23.3K
Replication in Eukaryotes
13.7K
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...
13.7K
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
DNA Damage can Stall the Cell Cycle
9.1K
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
9.1K
Homologous Recombination
50.4K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.4K
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
