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

Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

10.6K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.6K
Types of RNA01:20

Types of RNA

5.7K
Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in regulating gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
RNA Performs Diverse...
5.7K
Translational Regulation01:29

Translational Regulation

1
Translational regulation in prokaryotes ensures efficient protein synthesis by controlling ribosome access to mRNA. This regulation is mediated by secondary RNA structures, including translational riboswitches, RNA thermometers, and small RNAs (sRNAs), which respond to intracellular and environmental signals to modulate gene expression.Translational RiboswitchesRiboswitches in the leader region of mRNAs can regulate translation by altering the accessibility of the Shine-Dalgarno (SD) sequence,...
1
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

7.6K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
7.6K
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

873
The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the...
873
Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

22.5K
Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
Transcription results in the generation of precursor (pre-mRNA) that consists of both exons and introns, which needs further processing before being translated to a...
22.5K

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

AI platform for CRISPR functional mapping and function-based drug design.

bioRxiv : the preprint server for biology·2026
Same author

Alzheimer's disease risk protein SorLA regulates ER homeostasis and lipid metabolism in human microglia, with conserved effects in neurons.

Acta neuropathologica·2026
Same author

Decoding the <i>MYC</i> locus reveals a druggable ultraconserved RNA element.

bioRxiv : the preprint server for biology·2026
Same author

ADAMTS7 promotes smooth muscle foam cell expansion in atherosclerosis.

The Journal of clinical investigation·2026
Same author

Pathogenetic mechanisms of muscle-specific ribosomes in dilated cardiomyopathy.

Nature cardiovascular research·2026
Same author

Temporal Dynamics Between Daily Stress, Activity Choice, and Well-Being: An Experience Sampling Study.

Stress and health : journal of the International Society for the Investigation of Stress·2025
Same journal

Horizontal transfer of mitochondria in cancer: The physiology reborn in disease?

Trends in cell biology·2026
Same journal

Spindle errors: A stress test for epithelial robustness.

Trends in cell biology·2026
Same journal

Multicellular ecosystems: Linking cellular diversity to tissue function and disease.

Trends in cell biology·2026
Same journal

Orchestrating the signaling-bias at the protease-activated receptor, PAR1.

Trends in cell biology·2026
Same journal

Crashing by design: Utilizing DNA damage for MCC differentiation.

Trends in cell biology·2026
Same journal

The value of a shared lab: Our insights.

Trends in cell biology·2026
查看所有相关文章

相关实验视频

Updated: Jun 9, 2025

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs
10:37

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs

Published on: May 10, 2018

12.5K

抑制非编码翻译的机制

Jordan S Kesner1, Xuebing Wu1

  • 1Department of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA; Department of Systems Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.

Trends in cell biology
|October 23, 2024
PubMed
概括
此摘要是机器生成的。

细胞可以将非编码DNA转化为蛋白质,从而可能造成伤害. 本综述强调了BAG6通路如何抑制这种非编码翻译,保护细胞免受有毒蛋白质的产生.

关键词:
BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6 BAG6非编码的序列序列.没有编码的翻译.蛋白质质量控制 蛋白质质量控制核糖体的核糖体是指核糖体中的核糖体.

更多相关视频

Assessment of Selective mRNA Translation in Mammalian Cells by Polysome Profiling
10:00

Assessment of Selective mRNA Translation in Mammalian Cells by Polysome Profiling

Published on: October 28, 2014

28.2K
Xenopus laevis as a Model to Identify Translation Impairment
10:24

Xenopus laevis as a Model to Identify Translation Impairment

Published on: September 27, 2015

10.7K

相关实验视频

Last Updated: Jun 9, 2025

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs
10:37

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs

Published on: May 10, 2018

12.5K
Assessment of Selective mRNA Translation in Mammalian Cells by Polysome Profiling
10:00

Assessment of Selective mRNA Translation in Mammalian Cells by Polysome Profiling

Published on: October 28, 2014

28.2K
Xenopus laevis as a Model to Identify Translation Impairment
10:24

Xenopus laevis as a Model to Identify Translation Impairment

Published on: September 27, 2015

10.7K

科学领域:

  • 分子生物学分子生物学
  • 遗传学 遗传学 是一个
  • 细胞生物学 细胞生物学

背景情况:

  • 大多数基因组DNA是非编码的,但在这些区域发生翻译,包括长非编码RNA (lncRNA),UTR和内基因.
  • 从非编码序列中抑制翻译的细胞机制尚未得到充分理解.
  • 非编码序列的不受控制的翻译可以导致产生潜在的有毒蛋白质.

研究的目的:

  • 审查和总结已知的缓解非编码翻译机制.
  • 要突出BCL2-关联的阿坦基因6 (BAG6) 途径作为非编码翻译的关键抑制剂的作用.

主要方法:

  • 审查现有的关于非编码翻译及其监管的文献.
  • 对全基因组核糖体足迹数据的分析.
  • 专注于参与蛋白质抑制的蛋白质体降解途径.

主要成果:

  • 在注释的非编码基因组序列中观察到广泛的翻译.
  • 确定了与BCL2相关的阿坦基因6 (BAG6) 途径作为一个关键机制.
  • 通过BAG6介导的蛋白质体降解有效地抑制了来自各种非编码序列的翻译.

结论:

  • 由于有毒蛋白质合成,非编码翻译存在潜在风险.
  • BAG6通路代表了元动物细胞中保存的,统一的机制,以抑制非编码翻译.
  • 了解这些抑制机制对于理解细胞平衡和预防疾病至关重要.