Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

RNA-seq03:21

RNA-seq

9.7K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
9.7K
RNA Stability01:53

RNA Stability

33.1K
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...
33.1K
Ribosome Profiling02:24

Ribosome Profiling

3.4K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
3.4K
Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

9.1K
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...
9.1K
pre-mRNA Processing02:01

pre-mRNA Processing

52.4K
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...
52.4K
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

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

QutRNA2: robust tRNA modification discovery from Nanopore direct tRNA sequencing.

NAR genomics and bioinformatics·2026
Same author

Derivation of elephant induced pluripotent stem cells.

Nature methods·2026
Same author

Circtools 2.0: a comprehensive framework for enhanced circular RNA bioinformatics.

BMC bioinformatics·2026
Same author

Systematic benchmarking of dorado basecalling models for RNA modification detection with highly multiplexed nanopore sequencing.

Nucleic acids research·2026
Same author

Sex-specific regulation of angiogenin in Alzheimer's disease.

Molecular psychiatry·2026
Same author

FIRST-seq: a nanopore-based cDNA sequencing platform for RNA modification and structure profiling.

Genome biology·2026

相关实验视频

Updated: May 13, 2025

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study
06:57

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study

Published on: July 7, 2023

993

通过纳米孔测序来预测RNA修饰的RMaP挑战.

Jannes Spangenberg1, Stefan Mündnich2, Anne Busch3

  • 1RNA Bioinformatics, Friedrich-Schiller-University Jena, Leutragraben 1, 07743, Jena, Germany.

Communications chemistry
|April 12, 2025
PubMed
概括

经转录学研究正在推进新的计算方法来检测RNA修饰物,如N6-甲基氨酸 (m6A) 和伪氨酸 (ψ). RMaP挑战提高了RNA修饰预测的准确性,并突出了未来发展的领域.

更多相关视频

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

13.5K
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

1.8K

相关实验视频

Last Updated: May 13, 2025

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study
06:57

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study

Published on: July 7, 2023

993
Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

13.5K
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

1.8K

科学领域:

  • 史诗转录组学 史诗转录组学
  • 计算生物学 计算生物学
  • 生物信息学是一种生物信息学.

背景情况:

  • RNA修饰在细胞过程中起着至关重要的作用.
  • 直接RNA测序技术可以检测本地RNA中的这些修饰.
  • 计算机科学的整合对于推进表体转录学至关重要.

研究的目的:

  • 将科学家们聚集在一起,推进RNA修饰检测解决方案.
  • 讨论RNA修饰检测中的想法,问题和方法.
  • 提高RNA修饰预测算法的可比性,可靠性和一致性.

主要方法:

  • 利用了来自牛津纳米孔技术 (ONT) 的直接RNA测序数据.
  • 应用并比较了几种用于检测mRNA修饰的计算方法.
  • 专注于N6-甲基亚丁素 (m6A),伪尿素 (ψ) 和5-甲基细胞素 (m5C).

主要成果:

  • 在m6A, ψ和m5C.中实现了低预测误差和高预测准确性.
  • 证明了各种计算方法和算法的有效性.
  • 突出了计算方法在表体转录学中的潜力.

结论:

  • RMaP挑战显著提升了RNA修饰预测.
  • 计算方法在检测关键mRNA修改方面表现出高准确度.
  • 需要进一步的挑战来解决表皮转录组学的年轻领域的缺陷.