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相关概念视频

RNA Editing02:23

RNA Editing

9.2K
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...
9.2K
RNA Splicing01:32

RNA Splicing

56.9K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
56.9K
RNA Stability01:53

RNA Stability

33.9K
Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
33.9K
pre-mRNA Processing02:01

pre-mRNA Processing

53.4K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
53.4K
Transfer RNA Synthesis02:36

Transfer RNA Synthesis

12.2K
One of the unique features of tRNA is the presence of modified bases. In some tRNAs, modified bases account for nearly 20% of the total bases in the molecule. Altogether, these unusual bases protect the tRNA from enzymatic degradation by RNases.
Each of these chemical modifications is carried by a specific enzyme, post-transcription. All of these enzymes have unique base and site-specificity. Methylation, the most common chemical modification, is carried by at least nine different enzymes, with...
12.2K
Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

9.8K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
9.8K

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相关实验视频

Updated: Sep 10, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
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A Nonsequencing Approach for the Rapid Detection of RNA Editing

Published on: April 21, 2022

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转录和特定于时间的RNA核酸编辑技术.

Rushdhi Rauff1, Chanjuan Dong1, Shiva Ayyar1

  • 1Department of Chemistry, Case Western Reserve University, 2080 Adelbert Road, Cleveland, OH 44106, USA.

Bioorganic & medicinal chemistry
|August 19, 2025
PubMed
概括

研究人员正在开发新的工具,以精确控制RNA修饰,使得更深入地了解基因调节. 这些先进的技术克服了研究表观转录学早期方法的局限性.

关键词:
一到一的编辑.反意义的反意义科尔特斯 (Cirts) 是一个古老的品种.克里斯普尔是什么意思?克里斯普尔是什么意思?化学诱导的近距离关系表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.这是一个RNARNARNARNARNA.m5C 在线观看m6A 一个很好的.

更多相关视频

RNA Catalyst as a Reporter for Screening Drugs against RNA Editing in Trypanosomes
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RNA Catalyst as a Reporter for Screening Drugs against RNA Editing in Trypanosomes

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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

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相关实验视频

Last Updated: Sep 10, 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

2.7K
RNA Catalyst as a Reporter for Screening Drugs against RNA Editing in Trypanosomes
09:19

RNA Catalyst as a Reporter for Screening Drugs against RNA Editing in Trypanosomes

Published on: July 22, 2014

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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

Published on: July 10, 2020

2.0K

科学领域:

  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.
  • 生物化学 生物化学

背景情况:

  • 改性RNA核酸在转录后基因调节中起着至关重要的作用.
  • 传统上,研究表观转录学调节涉及改变RNA编辑酶表达的过程.
  • 全球修饰变化掩盖了单个RNA变化的特定场所效应.

研究的目的:

  • 提供当前空间时空控制的RNA核酸编辑技术的全面概述.
  • 要突出用于精确控制RNA修饰的新工具.
  • 为了解决研究局部特异性表皮转录学效应的局限性.

主要方法:

  • 审查新兴的RNA修饰编辑工具.
  • 讨论使用CRISPR,反感性寡核酸 (ASO),化学联体和光的技术.
  • 专注于能够精确控制RNA编辑的时间和空间的工具.

主要成果:

  • 新型RNA编辑工具可以选择性地将RNA编辑酶向特定的部位.
  • 这些工具允许对RNA修饰进行精确的时间控制.
  • 克里斯普,ASO,化学配体和基于光的方法是关键技术.

结论:

  • 时空控制的RNA编辑技术正在推进表观转录学研究.
  • 这些工具可以详细研究单个RNA修饰的影响.
  • 精确的控制有助于更深入地了解基因调节.