Jove
Visualize
お問い合わせ
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー

関連する概念動画

Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

15.1K
Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
15.1K
RNA Editing02:23

RNA Editing

8.8K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
8.8K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

5.9K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
5.9K
Proofreading01:31

Proofreading

6.1K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
6.1K
DNA-only Transposons02:57

DNA-only Transposons

14.3K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
14.3K
Mismatch Repair01:20

Mismatch Repair

4.7K
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...
4.7K

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Traceless protein semisynthesis in cells using the promiscuous ultra-fast split intein NrdJ-1.

Chemical science·2026
Same author

Traceless protein semi-synthesis in cells using the promiscuous ultra-fast split intein NrdJ-1.

bioRxiv : the preprint server for biology·2026
Same author

<i>Caenorhabditis elegans</i> avoids <i>Todstoff</i> , a novel nociceptive necrotaxis cue.

bioRxiv : the preprint server for biology·2026
Same author

A SWI/SNF-specific Ig-like domain, SWIFT, is a transcription factor binding platform.

Science (New York, N.Y.)·2026
Same author

Chromatin as a three-dimensional memory machine.

Current opinion in structural biology·2025
Same author

Programmable protein ligation on cell surfaces.

Nature·2025
Same journal

A native sulfur deposit in Gale crater, Mars.

Science (New York, N.Y.)·2026
Same journal

Coordinated demise of harmful algal blooms.

Science (New York, N.Y.)·2026
Same journal

Genetic effects put into context.

Science (New York, N.Y.)·2026
Same journal

Bacteria share proteins to survive antibiotics.

Science (New York, N.Y.)·2026
Same journal

Impacts shaped Earth's first continents.

Science (New York, N.Y.)·2026
Same journal

Erratum for the Report "Covalently bonded single-molecule junctions with stable and reversible photoswitched conductivity" by C. Jia <i>et al</i>.

Science (New York, N.Y.)·2026
関連記事をすべて見る

関連する実験動画

Updated: May 21, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
08:50

A Nonsequencing Approach for the Rapid Detection of RNA Editing

Published on: April 21, 2022

2.5K

調整された転置反応を用いたタンパク質編集

Yi Hua1, Nicholas E S Tay1, Xuanjia Ye1

  • 1Department of Chemistry, Princeton University, Princeton, NJ, USA.

Science (New York, N.Y.)
|April 3, 2025
PubMed
まとめ
この要約は機械生成です。

この研究は,タンパク質工学の新しい方法であるタンパク質転置を導入します. 固有の折り畳み条件下での内部タンパク質の直接的代替を可能にし,タンパク質半合成の応用を拡大します.

さらに関連する動画

CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.
07:46

CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.

Published on: December 11, 2020

5.7K
Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
09:51

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms

Published on: May 25, 2018

33.6K

関連する実験動画

Last Updated: May 21, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
08:50

A Nonsequencing Approach for the Rapid Detection of RNA Editing

Published on: April 21, 2022

2.5K
CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.
07:46

CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.

Published on: December 11, 2020

5.7K
Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
09:51

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms

Published on: May 25, 2018

33.6K

科学分野:

  • 生物化学
  • 分子生物学
  • タンパク質工学

背景:

  • ポリペプチド結合によるタンパク質工学は強力ですが 最終的な折り畳みステップが必要です
  • この制限は,タンパク質半合成に適したシステムの種類を制限する.

研究 の 目的:

  • 単一の操作で内部タンパク質を交換する方法を開発する.
  • タンパク質半合成の範囲を拡大し,ネイティブのタンパク質折り畳み条件下で編集を可能にします.

主な方法:

  • エンジニアリングされた分割インテインの正交配ペアを使用して,タンパク質転置システムを開発した.
  • この方法は,DNA転置に類似して,タンパク質編集を媒介する.
  • 折りたたまれたタンパク質複合体を含む 様々なシステムに この技術を適用した

主要な成果:

  • 単一のステップで標的タンパク質の内部部位を成功裏に置き換えた.
  • タンパク質にコード化されていない元素の効率的な導入を容易にした.
  • 折りたたまれたタンパク質複合体に対する 方法の適用性を実証した.

結論:

  • タンパク質のトランスポーゼーションは タンパク質の工学に多岐にわたるアプローチを提供する.
  • この方法は従来の結合戦略の限界を克服しています.
  • タンパク質の半合成と機能化の可能性を大幅に拡大する.