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相关概念视频

Ribosome Profiling02:24

Ribosome Profiling

4.1K
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.
The technique...
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RNA Editing02:23

RNA Editing

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RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
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Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

13.7K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
13.7K
RNA Stability01:53

RNA Stability

35.6K
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...
35.6K
pre-mRNA Processing02:01

pre-mRNA Processing

57.1K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
57.1K
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

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相关实验视频

Updated: Jan 14, 2026

Methylated RNA Immunoprecipitation Assay to Study m5C Modification in Arabidopsis
08:50

Methylated RNA Immunoprecipitation Assay to Study m5C Modification in Arabidopsis

Published on: May 14, 2020

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扩展Epitranscriptomics到非酶性RNA修饰

Kaila Nishikawa1,2, Yael David1,2,3,4, Anna Knörlein1

  • 1Chemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Trends in chemistry
|October 17, 2025
PubMed
概括
此摘要是机器生成的。

越来越多地认识到RNA上的非酶的共价修饰 (NECMs),与酶的不同. 本综述探讨了它们对RNA功能和潜在疾病联系的影响,突出了细胞调节的未经探索的领域.

关键词:
史诗转录组学 史诗转录组学修改 修改 修改 修改这是一个RNARNARNARNARNA.非酶性的非酶性.

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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

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Characterizing RNA Modifications in Single Neurons Using Mass Spectrometry
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相关实验视频

Last Updated: Jan 14, 2026

Methylated RNA Immunoprecipitation Assay to Study m5C Modification in Arabidopsis
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Methylated RNA Immunoprecipitation Assay to Study m5C Modification in Arabidopsis

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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
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2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

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Characterizing RNA Modifications in Single Neurons Using Mass Spectrometry
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Characterizing RNA Modifications in Single Neurons Using Mass Spectrometry

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科学领域:

  • 生物化学 生化学
  • 分子生物学分子生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.

背景情况:

  • 细胞利用蛋白质,DNA和RNA的可逆修饰来调节和控制命运,主要是通过酶.
  • 非酶对应变异 (NECM) 也通过与小分子的反应在生物分子上自发发生.
  • 虽然在蛋白质和DNA中进行了研究,但RNA NECM的生物学作用在很大程度上仍未被探索.

研究的目的:

  • 在RNA上调查已识别和预测的非酶共价变异.
  • 探索RNA NECM对RNA结构,稳定性和功能的影响.
  • 检查RNA NECM与人类疾病之间的潜在联系.

主要方法:

  • 对已识别和预测的RNA NECMs进行文献综述.
  • 对NECM对RNA的影响现有数据的分析.
  • 探索潜在的疾病关联和监管机制.

主要成果:

  • 已识别和预测的RNA NECM代表了一个重要的,未经研究的修饰类.
  • 这些修改可以改变RNA结构,稳定性和生物功能.
  • 新出现的证据表明,RNA NECMs与各种疾病之间存在潜在联系.

结论:

  • 对RNA的非酶对应性修饰是未来研究的关键领域.
  • 了解RNA NECM可以为细胞动力学和疾病病原发生提供新的见解.
  • 需要进一步研究RNA NECM的调控机制和功能后果.