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関連する概念動画

Fixed Action Patterns01:06

Fixed Action Patterns

16.1K
A fixed action pattern (FAP) is a specific, hard-wired sequence of behaviors that occurs in response to an external stimulus, called a sign stimulus. The behavior is “fixed” because it is essentially unchangeable—proceeding similarly across individuals of a species every time it occurs.
16.1K
Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

6.3K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
6.3K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.1K
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,...
5.1K
Alternative RNA Splicing02:18

Alternative RNA Splicing

20.5K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
20.5K
Actin Filament Depolymerization01:19

Actin Filament Depolymerization

3.0K
Actin filaments (F-actin) are composed of actin subunits. The dissociation of actin monomers can occur from either end of F-actin. The rate of dissociation is faster from the minus-end or the pointed end, where the actin subunits exist with a bound ADP, together known as ADP-actin. The depolymerization of F-actin is aided by proteins, including the actin-depolymerizing factor (ADF) and cofilin family of proteins, gelsolin, and glia maturation factor (GMF).
In F-actin, the ADF/cofilin proteins...
3.0K
GPCR Desensitization01:12

GPCR Desensitization

6.2K
G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
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関連する実験動画

Updated: May 5, 2026

Fluorescence Recovery After Photobleaching FRAP of Fluorescence Tagged Proteins in Dendritic Spines of Cultured Hippocampal Neurons
06:35

Fluorescence Recovery After Photobleaching FRAP of Fluorescence Tagged Proteins in Dendritic Spines of Cultured Hippocampal Neurons

Published on: April 16, 2011

56.0K

裸のレプリケーションフォークは,APRPArtを壊します.

Oscar Fernandez-Capetillo1, André Nussenzweig

  • 1Genomic Instability Group, Spanish National Cancer Research Centre (CNIO), Madrid 28029, Spain.

Cell
|November 26, 2013
PubMed
まとめ
この要約は機械生成です。

複製フォークの破裂は,単一鎖のDNA結合タンパク質RPAが枯渇したときに起こります. この発見は,高複製性ストレスを有するがんを理解するために極めて重要です.

さらに関連する動画

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs
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Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs

Published on: May 10, 2018

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Fluorescence Recovery after Photobleaching of Yellow Fluorescent Protein Tagged p62 in Aggresome-like Induced Structures
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Fluorescence Recovery after Photobleaching of Yellow Fluorescent Protein Tagged p62 in Aggresome-like Induced Structures

Published on: March 26, 2019

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関連する実験動画

Last Updated: May 5, 2026

Fluorescence Recovery After Photobleaching FRAP of Fluorescence Tagged Proteins in Dendritic Spines of Cultured Hippocampal Neurons
06:35

Fluorescence Recovery After Photobleaching FRAP of Fluorescence Tagged Proteins in Dendritic Spines of Cultured Hippocampal Neurons

Published on: April 16, 2011

56.0K
Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs
10:37

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs

Published on: May 10, 2018

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Fluorescence Recovery after Photobleaching of Yellow Fluorescent Protein Tagged p62 in Aggresome-like Induced Structures
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Fluorescence Recovery after Photobleaching of Yellow Fluorescent Protein Tagged p62 in Aggresome-like Induced Structures

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科学分野:

  • 分子生物学は分子生物学である.
  • 遺伝学 遺伝学とは
  • がん研究 がん研究

背景:

  • DNA複製は細胞分裂に不可欠である.
  • 複製フォークは停滞し,DNAの損傷につながる可能性があります.
  • 複製ストレスは癌の特徴です.

研究 の 目的:

  • 複製フォークの崩壊のメカニズムを調査するために.
  • 複製ストレス中にDNA二重鎖の断裂に寄与する要因を特定する.

主な方法:

  • トレド氏らによる研究. (2013) は,複製フォークの安定性を監視する実験を含む可能性が高い.
  • 単一鎖DNA結合タンパク質RPAのレベルを測定するアッセイがおそらく使用された.

主要な成果:

  • フォークの破裂は,RPAのプールが枯渇したときに起こります.
  • RPAの枯渇は,壊滅的なDNA二重鎖の断裂につながります.

結論:

  • RPAの利用可能性は,複製フォークの崩壊を防ぐために非常に重要です.
  • RPAのダイナミクスを理解することは,がんの起源と複製性ストレスに対する治療戦略の洞察を提供します.