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

Translational Regulation01:29

Translational Regulation

523
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,...
523
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

1.3K
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...
1.3K
Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

25.7K
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...
25.7K
Leaky Scanning02:28

Leaky Scanning

5.6K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.6K
Initiation of Translation02:33

Initiation of Translation

38.3K
Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
38.3K
Initiation of Translation02:33

Initiation of Translation

7.9K
7.9K

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

Unbend, correction of local beam-induced sample motion in cryo-EM images using a 3D spline model.

eLife·2026
Same author

A Unified Mechanism of +1 Ribosomal Frameshifting.

Cold Spring Harbor perspectives in biology·2026
Same author

Author Correction: Cryo-EM structure of a natural RNA nanocage.

Nature·2025
Same author

<i>In extracto</i> cryo-EM reveals eEF2 as a major hibernation factor on 60S and 80S particles.

bioRxiv : the preprint server for biology·2025
Same author

Decreased cytoplasmic crowding via inhibition of ribosome biogenesis can trigger Candida albicans filamentous growth.

Nature microbiology·2025
Same author

Structural mechanism of mRNA decoding by mammalian GTPase GTPBP1.

Nature communications·2025

相关实验视频

Updated: Jan 13, 2026

Quantitative Immunofluorescence to Measure Global Localized Translation
09:13

Quantitative Immunofluorescence to Measure Global Localized Translation

Published on: August 22, 2017

10.4K

5MPs对非AUG翻译监管的结构基础

Ximena Zottig, Chun-Ying Huang, Zahra Seraj

    bioRxiv : the preprint server for biology
    |January 9, 2026
    PubMed
    概括

    eIF5模仿蛋白 (5MPs) 通过限制非正规的起始码子使用来控制蛋白质的产生. 这项研究揭示了5MPs稳定了核糖体复合体,促进了mRNA扫描,并防止在错误的起点启动.

    科学领域:

    • 分子生物学分子生物学
    • 结构生物学 结构生物学
    • 遗传学 是一个遗传学.

    背景情况:

    • 细胞蛋白质组调节涉及在AUG或非正规 (非AUG) 起始编码子的翻译启动.
    • 非AUG启动在压力期间至关重要,并且与癌症等疾病有关.
    • eIF5模仿蛋白 (5MPs) 限制非AUG启动码子的使用,从具有替代启动地点的mRNA重新编程蛋白形表达.

    研究的目的:

    • 阐明5MPs诱导翻译重编程的机制.
    • 为了了解5MPs如何限制非AUG启动密码子的使用.

    主要方法:

    • 在抽取式冷电子显微镜 (cryo-EM) 中.
    • 生物化学测定 生物化学测定
    • 从原生细胞提取物中分析5MP结合的48S预启动复合物 (PIC).

    主要成果:

    • 通过5MP的转化抑制是依赖序列上下文的近期启动代码.
    • 低温-EM结构显示5MP结合在小核糖体亚单元的A位点,稳定一个开头的PIC形状.
    • 5MP的N终端区域阻断了A位点,而C终端域与P位点外的eIF2β和启动tRNA相互作用 (Pout).

    更多相关视频

    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

    11.1K
    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

    13.0K

    相关实验视频

    Last Updated: Jan 13, 2026

    Quantitative Immunofluorescence to Measure Global Localized Translation
    09:13

    Quantitative Immunofluorescence to Measure Global Localized Translation

    Published on: August 22, 2017

    10.4K
    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

    11.1K
    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

    13.0K

    结论:

    • 5MP直接偏向启动48S复合体向一个开放的形状.
    • 这种偏差促进了mRNA扫描,并抑制了在低于最佳的起始编码子的启动.
    • 这些发现为5MP介导的翻译控制提供了一个结构机制.