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相关概念视频

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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Rous Sarcoma Virus (RSV) and Cancer01:03

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Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
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Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

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Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
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RNA Polymerase II Accessory Proteins02:36

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Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
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Ribosome Profiling02:24

Ribosome Profiling

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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.
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Directing Proteins to the Rough Endoplasmic Reticulum01:34

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The organelle-specific signaling sequences direct proteins synthesized in the cytosol to their final destination like ER, mitochondria, peroxisomes, etc. Some of the proteins directed to ER are then trafficked via vesicles to other organelles within the cell or the extracellular environment through the Golgi complex. For example, the rough ER synthesizes soluble proteins for transportation to the lysosomes or secretion out of the cell. It can also synthesize transmembrane proteins that can...
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相关实验视频

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Optical Tweezers to Study RNA-Protein Interactions in Translation Regulation
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结构切换动态控制双重伪结的罗斯肉瘤病毒编程的核糖体框架转移元件.

Christopher P Jones1, Adrian R Ferré-D'Amaré1

  • 1Laboratory of Nucleic Acids, Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, Bethesda, MD 20892-8012.

Proceedings of the National Academy of Sciences of the United States of America
|April 2, 2025
PubMed
概括

逆转录病毒中编程的移,对于病毒蛋白平衡至关重要,由RNA结构控制. 研究人员解决了关键移元件的3D结构,揭示了这个过程中至关重要的动态双伪点.

关键词:
结构 RNA 结构 RNA 结构这是X射线.化学探测 化学探测 化学探测冰冷化EMEM可以使用.病毒RNA病毒RNA病毒RNA病毒RNA病毒RNA病毒RNA

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相关实验视频

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科学领域:

  • 结构生物学是结构生物学.
  • 病毒学 病毒学
  • 分子生物学分子生物学

背景情况:

  • 编程的-1转移对于逆转录病毒复制至关重要,控制病毒蛋白质静态度.
  • 来自罗斯肉瘤病毒的第一个发现的移刺激元素的3D结构在40年内仍然难以捉摸.

研究的目的:

  • 为了确定罗斯肉瘤病毒的3D结构,转移的刺激元素.
  • 阐明这个元素在调节编程移的结构-功能关系.

主要方法:

  • 低温电子显微镜 (cryo-electron microscopy) (低温电子显微镜) 是一种电子显微镜.
  • 在X射线晶体学.
  • 结构-功能分析分析.

主要成果:

  • RNA元素采用类似蝶的双重伪结折叠.
  • 一个关键的氨酸残留物 (A2546) 起到切换作用,切换形状并影响移效率高达50倍.
  • 结构揭示了形状异质性和动态交叉点.

结论:

  • 动态的双伪结结构通过利用形状异质性来刺激框架转移.
  • 支持一个多态模型,其中高的香农增强了移,是支持的.