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関連する概念動画

Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
LTR Retrotransposons03:08

LTR Retrotransposons

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...
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
Mechanisms of Retrovirus-induced Cancers01:51

Mechanisms of Retrovirus-induced Cancers

Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
Mechanisms of Retrovirus-induced Cancers01:51

Mechanisms of Retrovirus-induced Cancers

Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...

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関連する実験動画

Updated: Jul 15, 2026

Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites
09:31

Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites

Published on: March 22, 2016

レトロウイルスの統合のための非常に好ましいターゲット

C C Shih1, J P Stoye, J M Coffin

  • 1Tufts University School of Medicine, Department of Molecular Biology and Microbiology, Boston, Massachusetts 02111.

Cell
|May 20, 1988
PubMed
まとめ

レトロウイルスの宿主DNAへの統合は,複製に不可欠です. この研究は,Rousの肉腫ウイルスの標的となる特定の好ましいDNA配列を特定し,統合部位の特異性を明らかにしました.

科学分野:

  • 分子生物学は分子生物学である.
  • ウイルス学 ウイルス学 ウイルス学
  • 遺伝学 遺伝学とは

背景:

  • レトロウイルスの複製は,ウイルスDNA (プロウイルス) を宿主細胞のゲノムに統合することを意味します.
  • 統合中にレトロウイルスに標的となる正確なDNA配列は,完全に理解されていません.

研究 の 目的:

  • 宿主細胞DNAへのレトロウイルスの統合の特異性を調査する.
  • Rous サルコマウイルスの統合のための好ましい標的配列を特定する.

主な方法:

  • 多くの未選択のレトロウイルス統合イベントを分析するためのスクリーニング方法を開発しました.
  • 選択可能なマーカーで複製能力のあるロース肉腫ウイルスを利用しました.
  • ハイブリダイゼーションとシーケンシングを介して,統合されたプロウイルスと隣接ホストのDNA配列を分析した.

主要な成果:

  • 強烈に好ましい統合ターゲットであるいくつかのDNA配列モチーフを特定しました.
  • 優先ターゲット内の独立した統合イベントが,同一のベースポジションで発生することを実証した.
  • Rous サルコマウイルスの統合プロセスにおけるシーケンスの特異性を明らかにした.

さらに関連する動画

Bidirectional Retroviral Integration Site PCR Methodology and Quantitative Data Analysis Workflow
12:53

Bidirectional Retroviral Integration Site PCR Methodology and Quantitative Data Analysis Workflow

Published on: June 14, 2017

Retroviral Scanning: Mapping MLV Integration Sites to Define Cell-specific Regulatory Regions
10:10

Retroviral Scanning: Mapping MLV Integration Sites to Define Cell-specific Regulatory Regions

Published on: May 28, 2017

関連する実験動画

Last Updated: Jul 15, 2026

Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites
09:31

Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites

Published on: March 22, 2016

Bidirectional Retroviral Integration Site PCR Methodology and Quantitative Data Analysis Workflow
12:53

Bidirectional Retroviral Integration Site PCR Methodology and Quantitative Data Analysis Workflow

Published on: June 14, 2017

Retroviral Scanning: Mapping MLV Integration Sites to Define Cell-specific Regulatory Regions
10:10

Retroviral Scanning: Mapping MLV Integration Sites to Define Cell-specific Regulatory Regions

Published on: May 28, 2017

結論:

  • レトロウイルスの統合はランダムではなく,重要な配列偏好を示す.
  • 特定の宿主DNA配列は,プロウイルス統合中に,Rousの肉腫ウイルスの標的となる.
  • 統合特異性を理解することは,レトロウイルス複製機構の解読の鍵です.