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関連する概念動画

Telomeres and Telomerase02:41

Telomeres and Telomerase

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 DNA.
Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
Homologous Recombination02:31

Homologous Recombination

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...
DNA Helicases00:55

DNA Helicases

DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
Replication in Eukaryotes02:31

Replication in Eukaryotes

Overview

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関連する実験動画

Updated: Jun 25, 2026

A G-quadruplex DNA-affinity Approach for Purification of Enzymatically Active G4 Resolvase1
11:25

A G-quadruplex DNA-affinity Approach for Purification of Enzymatically Active G4 Resolvase1

Published on: March 18, 2017

人間のテロメアDNAの配列特異的な分裂は,G-四重複形成による.

Yan Xu1, Yuta Suzuki, Tuomas Lönnberg

  • 1Research Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan. xuyan@mkomi.rcast.u-tokyo.ac.jp

Journal of the American Chemical Society
|February 13, 2009
PubMed
まとめ

研究者らは,G-四重複形成を用いてヒトのテロメアDNAを標的とする新しい方法を開発した. このアプローチにより,配列特異のDNA分裂が可能になり,がん治療の開発のための新しい戦略を提供します.

科学分野:

  • バイオケミストリー バイオケミストリー
  • 分子生物学は分子生物学である.
  • 遺伝学 遺伝学とは

背景:

  • テロメアは染色体末端の保護キャップであり,がん生物学において極めて重要です.
  • テロメア機能不全は,がんの進行と老化に関与しています.
  • テロメアをターゲットにすることは,抗癌療法にとって有望な戦略です.

研究 の 目的:

  • ヒトのテロメアDNAのシーケンス固有の分裂のための構造ベースのアプローチを調査する.
  • テロメアを標的とするG-クアドルプレックス形成の可能性を調査する.
  • 新しいテロメアターゲティング反応剤の概念証明を確立する.

主な方法:

  • 5'端にマルチフォスフォナート [DNA-EDTP.Ce(IV] を含むオリゴヌクレオチドを使用する.
  • ヒトのテロメアDNAを結合するためにG-クアドルプレックス形成を用いる.
  • 設計されたオリゴヌクレオチド経由でシーケンス固有のDNA鎖の断裂を誘導する.

主要な成果:

  • [DNA-EDTP.Ce(IV) ]オリゴヌクレオチドは,G-四重複形成を通じてヒトのテロメアDNAにうまく結合する.
  • ヒトのテロメアDNAのシーケンス固有の分裂が達成されました.

さらに関連する動画

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
05:37

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes

Published on: April 4, 2025

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
08:28

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers

Published on: September 19, 2017

関連する実験動画

Last Updated: Jun 25, 2026

A G-quadruplex DNA-affinity Approach for Purification of Enzymatically Active G4 Resolvase1
11:25

A G-quadruplex DNA-affinity Approach for Purification of Enzymatically Active G4 Resolvase1

Published on: March 18, 2017

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
05:37

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes

Published on: April 4, 2025

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
08:28

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers

Published on: September 19, 2017

  • この研究は,G-四重複形成経由でヒトのテロメアDNAをターゲットにするための最初の証拠を提供します.
  • 結論:

    • 開発された方法は,配列特異のテロメアDNA分裂のための新しい戦略を示しています.
    • G-クアドルプレックス形成は,テロメアDNAをターゲットにするための有効なメカニズムです.
    • この研究は,がん治療のための高度なテロメア分裂剤の設計の基礎となる.