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 Splicing01:32

RNA Splicing

61.5K
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...
61.5K
RNA Splicing01:32

RNA Splicing

20.3K
20.3K
Pre-mRNA Processing: RNA Splicing01:32

Pre-mRNA Processing: RNA Splicing

7.4K
7.4K
Chromatin Structure and RNA Splicing02:41

Chromatin Structure and RNA Splicing

3.7K
3.7K
Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

3.5K
Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
3.5K
Alternative RNA Splicing02:18

Alternative RNA Splicing

27.0K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
27.0K

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

Structural basis of the regulation by CDK11 kinase of early spliceosome activation and evidence for its proofreading by DHX15 helicase.

Nature communications·2026
Same author

The co-localizing Zorya II, Druantia III, and ARMADA II defense systems on O-island 172 confer synergistic anti-phage defense in enterohemorrhagic <i>Escherichia coli</i>.

mBio·2026
Same author

Ski2-like helicase ASCC3 unwinds DNA upon fork stalling to control replication stress responses.

Cell reports·2026
Same author

The Ski2 helicase ASCC3 unwinds DNA upon fork stalling to control replication stress responses.

bioRxiv : the preprint server for biology·2025
Same author

Functional investigation of the RNA helicase MOV10 with respect to its interplay with factors involved in nonsense-mediated mRNA decay.

The Journal of biological chemistry·2025
Same author

The macromolecular crystallography beamlines of the Helmholtz-Zentrum Berlin at the BESSY II storage ring: history, current status and future directions.

Journal of synchrotron radiation·2025

相关实验视频

Updated: Apr 6, 2026

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast
07:31

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast

Published on: June 30, 2022

3.1K

快照:交叉体动力学III

Markus C Wahl1, Reinhard Lührmann2

  • 1Laboratory of Structural Biochemistry, Freie Universität Berlin, Takustraße 6, 14195 Berlin, Germany.

Cell
|August 2, 2015
PubMed
概括
此摘要是机器生成的。

由于突变导致的结合体功能障碍会导致疾病. 针对拼接的疗法,如小分子和反意义寡核酸,显示出有前途,并在临床试验中取得进展.

更多相关视频

A Reporter Based Cellular Assay for Monitoring Splicing Efficiency
08:53

A Reporter Based Cellular Assay for Monitoring Splicing Efficiency

Published on: September 15, 2021

3.4K
Utilization of Grafix for the Detection of Transient Interactors of Saccharomyces cerevisiae Spliceosome Subcomplexes
05:44

Utilization of Grafix for the Detection of Transient Interactors of Saccharomyces cerevisiae Spliceosome Subcomplexes

Published on: November 9, 2020

4.2K

相关实验视频

Last Updated: Apr 6, 2026

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast
07:31

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast

Published on: June 30, 2022

3.1K
A Reporter Based Cellular Assay for Monitoring Splicing Efficiency
08:53

A Reporter Based Cellular Assay for Monitoring Splicing Efficiency

Published on: September 15, 2021

3.4K
Utilization of Grafix for the Detection of Transient Interactors of Saccharomyces cerevisiae Spliceosome Subcomplexes
05:44

Utilization of Grafix for the Detection of Transient Interactors of Saccharomyces cerevisiae Spliceosome Subcomplexes

Published on: November 9, 2020

4.2K

科学领域:

  • 分子生物学
  • 遗传学
  • 药物发现

背景情况:

  • 一个复杂的分子机器spliceosome通过拼接来调节基因表达.
  • 结合因子或调节序列的突变会破坏结合体的功能.
  • 这种干扰与人类疾病有关,包括癌症和遗传性疾病.

研究的目的:

  • 探索合体动态的治疗潜力.
  • 审查目前用于调节疾病治疗的拼接事件的策略.

主要方法:

  • 关于结合体突变及其疾病关联的文献审查.
  • 分析治疗方法,包括小分子调制剂和反感性寡核酸.
  • 检查剪接调节剂的临床试验状态.

主要成果:

  • 发现了结合体功能障碍与各种人类病理之间强烈的联系.
  • 突出了小分子和反意义寡核酸作为治疗剂的潜力.
  • 在临床试验中注意到几种拼接调节疗法的进展.

结论:

  • 针对结合体动态为结合缺陷引起的疾病提供了有前途的治疗途径.
  • 进一步开发小分子调节剂和反感性寡核酸对于推进这些治疗非常重要.