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Phosphoinositides and PIPs01:42

Phosphoinositides and PIPs

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Phosphoinositides are a group of phospholipids containing a glycerol backbone with two fatty acid chains and a phosphate attached to a myoinositol sugar ring. The inositol head group extends into the cytoplasm, where it is modified by adding phosphate groups to form phosphatidylinositol phosphates or PIPs.
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
8.6K
Separation of Sister Chromatids02:17

Separation of Sister Chromatids

3.7K
At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
3.7K
The Phragmoplast01:59

The Phragmoplast

5.1K
Cell division is essential for organismal growth and development. In animal cells, the central spindle and its associated proteins form the midbody, a structure that has an essential role in cytokinesis. In plants, the central spindle, along with the microtubules, actin, and other cell components, matures into the phragmoplast, which is necessary for cytokinesis. Unlike the stationary midbody, the phragmoplast expands centrifugally, eventually leading to the formation of the new cell wall.
The...
5.1K
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

12.1K
Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and...
12.1K
Anaphase Promoting Complex00:50

Anaphase Promoting Complex

2.9K
The stepwise destruction of specific proteins is necessary for the progression and completion of the cell cycle. Such proteins are ubiquitinated by ubiquitin ligases and then subsequently destroyed by the proteasome. The SCF (Skp1/Cullin/F-box) and the anaphase-promoting complex (APC) are two important ubiquitin ligases involved in cell cycle progression. While SCF is active throughout the cell cycle, APC gets activated during metaphase to anaphase transition. Cdc20 or Cdh1 binds to APC and...
2.9K
Cell Polarization by Rho Proteins01:21

Cell Polarization by Rho Proteins

2.7K
Cell polarity is the asymmetric distribution of cellular and membrane components, making one side of the cell different from the other. This polarity is essential to many processes such as embryogenesis, axon migration, glucose transport across epithelial cells, and directional cell migration. A migrating cell responds to intracellular or extracellular signals via molecular cascades that reorganize the actin cytoskeleton to establish this polarity. In these cells, the Rho family proteins Cdc42,...
2.7K

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Updated: Jul 12, 2025

"Phagosome Closure Assay" to Visualize Phagosome Formation in Three Dimensions Using Total Internal Reflection Fluorescent Microscopy TIRFM
10:07

"Phagosome Closure Assay" to Visualize Phagosome Formation in Three Dimensions Using Total Internal Reflection Fluorescent Microscopy TIRFM

Published on: August 26, 2016

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PHF1通过相位分离将PRC2进行分隔.

Genzhe Lu1,2,3, Pilong Li1,2

  • 1Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, Beijing 100084, China.

The Biochemical journal
|October 27, 2023
PubMed
概括
此摘要是机器生成的。

像PHF1这样的多样蛋白 (PCL) 在目标部位形成相分离的凝结物. 这些凝结物招募Polycomb镇压复合体2 (PRC2) 来存储H3K27me3标记并抑制转录.

关键词:
PHF1 PHF1 的时间在 PRC2 中,PRC2 是 PRC2 的第一个类型.阶段分离的阶段分离.

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Single-molecule Super-resolution Imaging of Phosphatidylinositol 4,5-bisphosphate in the Plasma Membrane with Novel Fluorescent Probes
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Single-molecule Super-resolution Imaging of Phosphatidylinositol 4,5-bisphosphate in the Plasma Membrane with Novel Fluorescent Probes

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Chemical Dimerization-Induced Protein Condensates on Telomeres
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Chemical Dimerization-Induced Protein Condensates on Telomeres

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相关实验视频

Last Updated: Jul 12, 2025

"Phagosome Closure Assay" to Visualize Phagosome Formation in Three Dimensions Using Total Internal Reflection Fluorescent Microscopy TIRFM
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"Phagosome Closure Assay" to Visualize Phagosome Formation in Three Dimensions Using Total Internal Reflection Fluorescent Microscopy TIRFM

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Single-molecule Super-resolution Imaging of Phosphatidylinositol 4,5-bisphosphate in the Plasma Membrane with Novel Fluorescent Probes
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Single-molecule Super-resolution Imaging of Phosphatidylinositol 4,5-bisphosphate in the Plasma Membrane with Novel Fluorescent Probes

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Chemical Dimerization-Induced Protein Condensates on Telomeres
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Chemical Dimerization-Induced Protein Condensates on Telomeres

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科学领域:

  • 表观遗传学和基因调控
  • 分子生物学分子生物学
  • 细胞生物学 细胞生物学

背景情况:

  • 聚合物抑制复合物2 (PRC2) 沉积基因组H3素27三甲基化 (H3K27me3),这是基因沉默的关键表观遗传标记.
  • 在特定的基因组位置PRC2的招募机制仍然不完全理解.
  • 聚类蛋白 (PCL) 是已知的辅助因素,可以影响PRC2向.

研究的目的:

  • 研究PCL蛋白PHF1在PRC2.2的招募和功能中的作用.
  • 阐明PHF1调解PRC2向和活动的分子机制.
  • 为了确定PHF1介导的相分离是否影响转录抑制.

主要方法:

  • 细胞成像和观察技术.
  • 生物化学复制试验. 生物化学复制试验.
  • 路西法雷斯记者测定用于基因表达分析.

主要成果:

  • PHF1在H3K27me3标记的位置形成分相冷凝.
  • 这些凝结物招募PRC2,特定的PHF1域调解目标识别,PRC2结合和相分离.
  • PHF1凝聚物分隔PRC2,DNA和核细胞,通过相位分离促进转录抑制.

结论:

  • PHF1驱动在目标位置形成生物分子凝聚物.
  • 这些凝结物作为招募和缩PRC2的平台,促进H3K27me3沉积和基因沉默.
  • PHF1介导的相分离是一种调节多抑制和基因转录的新机制.