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相关概念视频

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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Experimental RNAi02:15

Experimental RNAi

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RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
6.1K
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.
The technique...
3.5K
RNA-seq03:21

RNA-seq

10.0K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

29.6K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
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Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

9.3K
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...
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相关实验视频

Updated: Jul 11, 2025

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

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

Published on: July 10, 2020

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使用比较基因组学方法发现RNA修饰酶.

Satoshi Kimura1

  • 1Brigham and Women's Hospital, Department of Medicine, Division of Infectious Diseases, Boston, MA, USA; Harvard Medical School, Department of Microbiology, Boston, MA, USA.

Methods in enzymology
|November 4, 2023
PubMed
概括

这项研究提出了一个计算比较基因组学协议,以发现RNA修饰酶. 它成功识别了AcpA,一个负责合成acacp3U修饰的酶.

科学领域:

  • 分子生物学分子生物学
  • 基因组学就是基因组学.
  • 生物化学 生化学

背景情况:

  • 识别RNA修饰酶对于理解RNA生物发生和功能至关重要.
  • 比较基因组学为酶发现提供了一个强大的方法,利用丰富的基因组数据.
  • 目前用于识别RNA修饰酶的现有方法正在通过计算策略得到增强.

研究的目的:

  • 介绍一个详细的计算比较基因组学协议,用于发现新的RNA修饰酶.
  • 通过识别特定的酶和RNA修饰来证明这种方法的实用性.
  • 突出这一计算框架对其他细胞过程的更广泛适用性.

主要方法:

  • 开发和描述一个计算比较基因组学协议.
  • 该协议的应用用于识别RNA修饰酶.
  • 使用AcpA的发现和acacp3U修改的说明性示例.

主要成果:

  • 提供了基于计算比较基因组学的RNA修饰酶发现的详细协议.
  • 这种方法导致识别了AcpA,一种乙转移酶.
  • 证实AcpA是负责合成新型acacp3U修饰的酶.
关键词:
这是一次爆炸式爆炸.生物信息学是一种生物信息学.进行比较的基因组学.这是一个RNARNARNARNARNA.RNA修饰酶是RNA修饰酶的一个组成部分.

更多相关视频

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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DNAzyme-dependent Analysis of rRNA 2’-O-Methylation
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DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

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相关实验视频

Last Updated: Jul 11, 2025

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

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

Published on: July 10, 2020

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

Published on: May 14, 2020

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DNAzyme-dependent Analysis of rRNA 2’-O-Methylation
09:12

DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

Published on: September 16, 2019

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结论:

  • 计算比较基因组学为识别RNA修饰酶提供了一个有效的框架.
  • 提出的协议有助于发现参与RNA修饰途径的酶.
  • 这种方法在超越RNA修饰的多种细胞过程中识别基因的潜在应用.