関連する実験動画
Updated: May 14, 2026

10:59
Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
Published on: August 21, 2021
プログラムされたDNA病変と免疫系におけるゲノム不安定のメカニズム
Frederick W Alt1, Yu Zhang, Fei-Long Meng
1Departments of Genetics and Pediatrics, Harvard Medical School, Boston, MA 02115, USA. alt@enders.tch.harvard.edu
Cell
|February 5, 2013
まとめ
リンパ性悪性腫瘍は,リンパ細胞のDNA二重鎖断裂 (DSB) から生じる染色体転位をしばしば含む. DSBの修復とゲノム組織を理解することは,これらのがんを予防する鍵です.
科学分野:
- 遺伝学 遺伝学とは
- 分子生物学は分子生物学である.
- がん研究 がん研究
背景:
- 染色体転位は,リンパ性悪性腫瘍で頻繁に見られます.
- これらの転位は,特定の染色体部位におけるDNA二重鎖断裂 (DSB) から生じる.
- リンパ球の発達には,DSBsを生成するプログラムされたゲノム変化が含まれています.
研究 の 目的:
- DSBsを生成するリンパ球特有のメカニズムについて議論します.
- DSBのターゲット特異性がどのように達成されるかを探求する.
- 転位を抑制するメカニズムと,DSB修復とゲノム組織に関する洞察を検証する.
主な方法:
- リンパ性悪性腫瘍における染色体転位に関する既存の文献のレビュー.
- リンパ球におけるプログラムされたゲノム変異の分析.
- DNA二重鎖断裂 (DSB) 修復経路と3Dゲノム組織についての議論.
主要な成果:
- リンパ球特異的なプロセスは,免疫受容体の多様性にとって不可欠なDSBを生成します.
- DSBをターゲットにし,転位を抑制するためのメカニズムが存在します.
- 最近の研究は,DSB修復とゲノム組織の役割に光を当てています.
結論:
- リンパ球におけるDSBの生成と修復を理解することは,リンパ球がん研究にとって極めて重要です.
- 3次元のゲノム組織は,生理学的プロセスと癌の発達の両方に影響を与えます.
- DSB経路をターゲットにすることで,リンパ性悪性腫瘍の治療戦略を提供することができる.
関連する概念動画
Overview of DNA Repair
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Chemically...
Overview of DNA Repair
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Chemically...
Nucleotide Excision Repair
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Nucleotide Excision Repair
Overview
Nucleotide Excision Repair
Overview
Spontaneous and Induced Mutations
Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).

