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相关概念视频

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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相关实验视频

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

对于复原病毒集成的高度首选的目标.

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
概括

逆转录病毒融入宿主DNA对于复制至关重要. 这项研究确定了Rous瘤病毒准的特定首选DNA序列,揭示了整合部位的特异性.

科学领域:

  • 分子生物学分子生物学
  • 病毒学 病毒学
  • 遗传学 是一个遗传学.

背景情况:

  • 回复病毒复制涉及将病毒DNA (前病毒) 整合到宿主细胞基因组中.
  • 在整合过程中,逆转录病毒所准的精确DNA序列尚未完全理解.

研究的目的:

  • 为了研究逆转录病毒融入宿主细胞DNA的特异性.
  • 为了确定Rous瘤病毒集成的首选目标序列.

主要方法:

  • 开发了一种查方法来分析许多未经选择的逆转录病毒整合事件.
  • 使用了具有可选择标记的复制能力的Rous瘤病毒.
  • 通过杂交和测序分析了集成的前病毒和侧面宿主DNA序列.

主要成果:

  • 确定了几种强烈喜欢的整合目标的DNA序列动机.
  • 证明优先目标中的独立整合事件发生在相同的基点位置.
  • 揭示了Rous肉瘤病毒集成过程中的序列特异性.

结论:

  • 复原病毒的整合不是随机的,并且表现出显著的序列偏好.
  • 特定的宿主DNA序列是Rous肉瘤病毒在前病毒集成期间的目标.

更多相关视频

Bidirectional Retroviral Integration Site PCR Methodology and Quantitative Data Analysis Workflow
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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

相关实验视频

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

  • 了解整合特异性是破译复原病毒复制机制的关键.