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相关概念视频

Condensins02:15

Condensins

3.7K
Condensins are large protein complexes that use ATP to fuel the assembly of chromosomes during mitosis. They transform the tangled, shapeless mass of post-interphase DNA into individualized chromosomes by compacting, organizing, and segregating chromosomal DNA.
The plant and animal cells contain two types of condensin complexes—condensin I and condensin II. Both complexes have five subunits: two SMC (Structural Maintenance of Chromosomes) subunits, a kleisin subunit, and two HEAT-repeat...
3.7K
Chromatin Packaging01:32

Chromatin Packaging

17.3K
Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
17.3K
Cohesins02:20

Cohesins

4.7K
Cohesin protein complexes are a molecular glue that holds two sister chromatids together. They play an important role both in mitosis and meiosis. In mitosis, all cohesin complexes present on the chromosomes are removed before the start of the anaphase stage.
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of...
4.7K
Forces Acting on Chromosomes02:11

Forces Acting on Chromosomes

3.4K
During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis. 
Microtubules and motor proteins exert two types of forces on...
3.4K
Attachment of Sister Chromatids02:57

Attachment of Sister Chromatids

3.4K
As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules.  Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall...
3.4K
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

8.5K
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...
8.5K

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相关实验视频

Updated: Sep 15, 2025

Associated Chromosome Trap for Identifying Long-range DNA Interactions
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Associated Chromosome Trap for Identifying Long-range DNA Interactions

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凝素加速长距离的染色体内相互作用.

Fan Zou1,2, Yi Li2,3, Timothy Földes4

  • 1Department of Physics, The Pennsylvania State University, University Park, PA 16802, USA.

bioRxiv : the preprint server for biology
|July 14, 2025
PubMed
概括

凝驱动酵母中的快速染色体内相互作用,与凝不同. 这揭示了凝素在3D基因组组织和活细胞染色质动态中的新作用.

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科学领域:

  • 基因组学就是基因组学.
  • 细胞生物学 细胞生物学
  • 生物物理学的生物物理.

背景情况:

  • 3D基因组组织调节了基因相互作用.
  • 染色体构造捕获 (3C) 方法提供静态视图.
  • 活细胞的染色质动力学是很少理解的.

研究的目的:

  • 在活酵母中测量染色体碰撞动力学.
  • 研究蛋白质复合体在基因组组织中的作用.
  • 描述染色体内和染色体间相互作用的动态.

主要方法:

  • 化学诱导的染色体相互作用 (CICI) 用于活细胞测量.
  • 有针对性的枯竭实验,以评估蛋白质复合体的功能.
  • 用Hi-C分析进行全基因组相互作用映射.
  • 聚合物模拟以建模染色质挤出.

主要成果:

  • 染色体运动与罗斯聚合物模型保持一致.
  • 长距离的染色体内接触比染色体间接触更快.
  • 素,而不是凝聚素,调解了快速的染色体内相互作用.
  • 凝素以约2kb/s的速度挤出色素.

结论:

  • 凝固素在基因组间阶段组织中发挥着新的作用.
  • 素促进了快速的长距离染色体内相互作用.
  • 提供了对3D基因组动态和体内染色体搜索策略的新见解.