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Spontaneous and Induced Mutations01:30

Spontaneous and Induced Mutations

241
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).
241
Mutations01:35

Mutations

40.5K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
40.5K
Mutagenicity and Carcinogenicity01:25

Mutagenicity and Carcinogenicity

1.4K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.4K
Mismatch Repair01:20

Mismatch Repair

5.3K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
5.3K
Nucleotide Excision Repair01:38

Nucleotide Excision Repair

3.9K
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...
3.9K
Epigenetic Regulation01:37

Epigenetic Regulation

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Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
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  2. ゲノムと化学療法による生殖線ハイパーミューテーションの影響
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  2. ゲノムと化学療法による生殖線ハイパーミューテーションの影響

関連する実験動画

Assessing Somatic Hypermutation in Ramos B Cells after Overexpression or Knockdown of Specific Genes
08:12

Assessing Somatic Hypermutation in Ramos B Cells after Overexpression or Knockdown of Specific Genes

Published on: November 1, 2011

20.1K

ゲノムと化学療法による生殖線ハイパーミューテーションの影響

Joanna Kaplanis1, Benjamin Ide2, Rashesh Sanghvi1

  • 1Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.

Nature
|May 11, 2022

PubMed で要約を見る

まとめ
この要約は機械生成です。

遺伝子の変異は 進化と病気を駆り立てます この研究では 12のゲノムで DNA修復遺伝子変異や 化学療法への曝露などの 父の要因に 関連した希少なハイパーミューテーションが 発見されました

さらに関連する動画

Analysis of Somatic Hypermutation in the JH4 intron of Germinal Center B cells from Mouse Peyer's Patches
09:35

Analysis of Somatic Hypermutation in the JH4 intron of Germinal Center B cells from Mouse Peyer's Patches

Published on: April 20, 2021

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Transgenic Rodent Assay for Quantifying Male Germ Cell Mutant Frequency
14:45

Transgenic Rodent Assay for Quantifying Male Germ Cell Mutant Frequency

Published on: August 6, 2014

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関連する実験動画

Assessing Somatic Hypermutation in Ramos B Cells after Overexpression or Knockdown of Specific Genes
08:12

Assessing Somatic Hypermutation in Ramos B Cells after Overexpression or Knockdown of Specific Genes

Published on: November 1, 2011

20.1K
Analysis of Somatic Hypermutation in the JH4 intron of Germinal Center B cells from Mouse Peyer's Patches
09:35

Analysis of Somatic Hypermutation in the JH4 intron of Germinal Center B cells from Mouse Peyer's Patches

Published on: April 20, 2021

6.9K
Transgenic Rodent Assay for Quantifying Male Germ Cell Mutant Frequency
14:45

Transgenic Rodent Assay for Quantifying Male Germ Cell Mutant Frequency

Published on: August 6, 2014

16.4K

科学分野:

  • 遺伝学
  • ゲノミクス
  • 進化生物学

背景:

  • 細菌系変異は 遺伝的変異と病気の源です
  • 親の年齢は新しい生殖遺伝子の変異に影響を与える 重要な要因です

研究 の 目的:

  • ヒトの生殖系統ゲノムにおける超変異の発生と原因を調査する.
  • 希少な遺伝疾患を持つ家族における全ゲノム配列を分析し,超変異した個体を特定する.

主な方法:

  • ゲノム全体で2万879の家族を 解析した
  • de novo単核型変異の分析について
  • 変異率が著しく高い個体を特定する.

主要な成果:

  • ゲノムが多変異した12人の個体 (予想されるde novo変異の2〜7倍) を特定した.
  • 過剰な突然変異は12家族のうち9家族で 主に父親から発生しました
  • 遺伝的誘導因子 (DNA修復遺伝子変異体) と環境因子 (化学療法) を特定した.

結論:

  • ゲルムラインは通常,ミュータジェニック効果に対して良好に保護されています.
  • 超変異は稀な現象で 変異数が少なすぎます
  • ハイパーミューテーションしたゲノムを持つ人のほとんどは 遺伝的疾患を呈しません