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関連する概念動画

Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

16.3K
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...
16.3K
DNA-only Transposons02:57

DNA-only Transposons

16.0K
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...
16.0K
LTR Retrotransposons03:08

LTR Retrotransposons

18.1K
LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
18.1K
Energy to Drive Translocation01:37

Energy to Drive Translocation

2.0K
Mitochondrial protein import is powered by two distinct energy sources: ATP hydrolysis and electrochemical potential across the inner membrane. Newly synthesized precursors are bound by cytosolic chaperones of the Hsp70 family, which guide them to the import receptors on the mitochondrial surface. Utilizing the energy of ATP hydrolysis, Hsp70 chaperones transfer these precursors to the TOM receptors on the mitochondrial outer membrane.
Generally, polypeptides are unfolded by two distinct...
2.0K
Protein Transport into the Inner Mitochondrial Membrane01:34

Protein Transport into the Inner Mitochondrial Membrane

3.5K
Nuclear encoded mitochondrial precursors are imported to the inner membrane in a multistep process involving two separate translocons, TIM22 and TIM23. TIM23 is a cation-selective pore that remains closed by the N terminal segment of the protein. Negative charges on the TIM23 act as a receptor for the incoming precursor, pulling the positively charged matrix-targeting sequence for peptide insertion and translocation.
Transport of mitochondrial precursors across the TIM23 channel is driven by...
3.5K
Transposons01:24

Transposons

3.2K
Transposons, or "jumping genes," are small mobile genetic elements (MGEs) that range from 700 to 40,000 base pairs in length. They are found in all organisms and can move within the same chromosome or transfer to different chromosomes. In some cases, transposons can also jump between different host DNA molecules, such as plasmids or viruses, contributing to genetic variability.Barbara McClintock first discovered these mobile genetic elements in the 1940s while studying maize genetics, and she...
3.2K

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関連する実験動画

Updated: May 2, 2026

Generation of Enterobacter sp. YSU Auxotrophs Using Transposon Mutagenesis
13:31

Generation of Enterobacter sp. YSU Auxotrophs Using Transposon Mutagenesis

Published on: October 31, 2014

13.3K

Tn10による分子内転移である.

H W Benjamin1, N Kleckner

  • 1Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.

Cell
|October 20, 1989
PubMed
まとめ

トランポゾンTn10は,分子内転移によって円形のDNA製品を形成する. 修復されていない結合は,この非複製プロセスに特定のタンパク質保護メカニズムが関与していることを示唆しています.

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
  • 微生物学 微生物学とは

背景:

  • トランポゾンは,ゲノム内の位置を変えることができる移動性遺伝的要素です.
  • トランポゾンTn10は,そのトランポジションメカニズムで知られているよく研究された例です.
  • 転置を理解することは,遺伝子調節とゲノム安定性にとって極めて重要です.

研究 の 目的:

  • トランポゾンTn10.0による円形のDNA産物形成のメカニズムを解明する.
  • 分子内転移の際の鎖裂けと結合の分子詳細を調査する.
  • Tn10トランスポーゼーションの非複製性に寄与する要因を特定する.

主な方法:

  • トランポゾンTn10によって生成された円形のDNA産物の分析.
  • DNA分裂と結合のモデルを用いたトランポゾン/標的の結合の特徴化.
  • 鎖移転接点におけるタンパク質-DNA相互作用の調査.

主要な成果:

  • 循環産物は,トランポゾン/標的の結合が修復されていない分子内転移から生じる.
  • 標的DNAの段階的なニックとトランポゾン端の割れ目を伴うモデルは,交差点構造を正確に予測します.

さらに関連する動画

Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
08:19

Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing

Published on: July 7, 2020

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Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity
04:04

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity

Published on: January 20, 2023

2.3K

関連する実験動画

Last Updated: May 2, 2026

Generation of Enterobacter sp. YSU Auxotrophs Using Transposon Mutagenesis
13:31

Generation of Enterobacter sp. YSU Auxotrophs Using Transposon Mutagenesis

Published on: October 31, 2014

13.3K
Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
08:19

Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing

Published on: July 7, 2020

9.8K
Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity
04:04

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity

Published on: January 20, 2023

2.3K
  • 非結合結節は安定しており,トランスポーゼおよび/または宿主タンパク質による保護を示唆しています.
  • 結論:

    • Tn10トランスポジションの非複製性には,移転されていないトランスポゾン鎖の分離が影響する.
    • 鎖移転接点のタンパク質-DNA複合体は,転置結果を決定する上で重要な役割を果たします.
    • Tn10トランスポーゼーションは,精密なDNA分裂と結合を伴い,その後,タンパク質媒介による中間物質の安定化が行われます.