相关实验视频
Updated: Jun 6, 2026

10:55
Study of the DNA Damage Checkpoint using Xenopus Egg Extracts
Published on: November 5, 2012
一种类似cdc2的蛋白质参与了Xenopus蛋提取物中DNA复制的启动
Cell
|September 7, 1990
概括
克塞诺普斯蛋提取物启动DNA复制. 削减p34cdc2蛋白质会阻止启动,但不会延长,这表明它在启动真核生物中的DNA复制中起着至关重要的作用.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 染色体DNA复制是细胞分裂的一个基本过程.
- 细胞周期控制着DNA复制的精确时间.
- 鸟蛋提取物提供了一个无细胞系统,用于研究DNA复制.
研究的目的:
- 研究Xenopus p34cdc2在启动染色体DNA复制中的作用.
- 为了确定p34cdc2是否在体外对DNA复制启动至关重要.
主要方法:
- 用于Xenopus蛋提取物进行体外DNA复制试验.
- 从使用亲和力枯竭 (p13suc1) 或免疫力枯竭的提取物中获得枯竭的p34cdc2.
- 在耗尽和复制的提取物中评估了DNA复制的启动和延长.
主要成果:
- 缺乏p34cdc2的提取物未能启动DNA复制,但支持延长.
- 核组装通常发生在耗尽的提取物中.
- 重新添加p34cdc2恢复了DNA复制的启动.
结论:
- Xenopus p34cdc2对于启动染色体DNA复制是必不可少的.
- p34cdc2在启动阶段运行,独立于核组装.
- 这些发现突显了p34cdc2在真核细胞循环调节中的保留作用.
相关概念视频
Replication in Eukaryotes
Overview
The Replisome
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
Restarting Stalled Replication Forks
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, a...
S-Cdk Initiates DNA Replication
The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.
Replication in Eukaryotes
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...
S-Cdk Initiates DNA Replication
The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.

