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相关概念视频

Translational Regulation01:29

Translational Regulation

108
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,...
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Leaky Scanning02:28

Leaky Scanning

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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...
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Chromatin Structure Regulates pre-mRNA Processing02:41

Chromatin Structure Regulates pre-mRNA Processing

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In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
The chromatin structure, especially...
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Protein Modifications in the RER01:26

Protein Modifications in the RER

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Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
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Riboswitches01:56

Riboswitches

8.7K
Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
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RNA Stability01:53

RNA Stability

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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...
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相关实验视频

Updated: Sep 17, 2025

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC
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通过对含有二硫化物的基组的结构优化加速响应性RNA释放.

Junsong Guo1, Senfeng Zhang2, Tuan-Khoa Kha1

  • 1Department of Chemistry, National University of Singapore, 4 Science Drive 2, Singapore, 117544, Singapore.

Angewandte Chemie (International ed. in English)
|June 28, 2025
PubMed
概括

一种新的化学方法使用氧化还原反应性RNA修饰来暂时阻止RNA功能. 谷氨 (GSH) 触发释放,恢复各种RNA类型的生物活性,包括信使RNA (mRNA).

关键词:
硫化二氧化物是二硫化物中的一种.这是GSHGSH.通过合成后的化.这是一个RNARNARNARNARNA.具有回应性去氧化剂.

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Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
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Identification of RNA Fragments Resulting from Enzymatic Degradation using MALDI-TOF Mass Spectrometry
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相关实验视频

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Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
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Identification of RNA Fragments Resulting from Enzymatic Degradation using MALDI-TOF Mass Spectrometry
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科学领域:

  • 化学生物学 化学生物学
  • 在RNA治疗方面,RNA疗法.
  • 生物化学 生物化学

背景情况:

  • 对RNA的化学修饰对于生物学研究和应用至关重要.
  • 合成后的2'-OH化允许按需激活RNA,但面临着更大的RNA的挑战.

研究的目的:

  • 开发一种可通用的氧化还原反应性RNA修饰策略,用于功能化不同长度的RNA.
  • 使用内源刺激,使无痕RNA释放和功能恢复成为可能.

主要方法:

  • 开发了三种后合成乙化策略,在2'-OH位置引入含二硫化物添加物.
  • 利用谷氨 (GSH) 触发转基因RNA的释放.
  • 在各种RNA结构中证明适用性,包括合成RNA,sgRNA和mRNA.

主要成果:

  • 成功引入多个含有二硫化物的乙烯添加物,暂时抑制RNA功能.
  • 展示了无痕迹的RNA释放和在暴露于GSH后恢复功能.
  • 在没有细胞毒性刺激的情况下实现了内源性GSH响应的mRNA翻译恢复.

结论:

  • 介绍一种简单且广泛适用的方法来修改和调节RNA功能.
  • 乙基组的结构优化促进RNA释放,增强多功能性.
  • 这一战略有可能推动基于RNA的治疗和研究.