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相关概念视频

Transfer RNA Synthesis02:36

Transfer RNA Synthesis

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One of the unique features of tRNA is the presence of modified bases. In some tRNAs, modified bases account for nearly 20% of the total bases in the molecule. Altogether, these unusual bases protect the tRNA from enzymatic degradation by RNases.
Each of these chemical modifications is carried by a specific enzyme, post-transcription. All of these enzymes have unique base and site-specificity. Methylation, the most common chemical modification, is carried by at least nine different enzymes, with...
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tRNA Activation02:26

tRNA Activation

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Aminoacyl-tRNA synthetases are present in both eukaryotes and bacteria. Though eukaryotes have 20 different aminoacyl-tRNA synthetases to couple to 20 amino acids, many bacteria do not have genes for all of these aminoacyl-tRNA synthetases. Despite this, they still use all 20 amino acids to synthesize their proteins. For instance, some bacteria do not have the gene encoding the enzyme that couples glutamine with its partner tRNA. In these organisms, one enzyme adds glutamic acid to all of the...
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Types of RNA01:20

Types of RNA

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Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in regulating gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
RNA Performs Diverse...
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pre-mRNA Processing02:01

pre-mRNA Processing

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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...
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Initiation of Translation02:33

Initiation of Translation

34.2K
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...
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From DNA to Protein03:06

From DNA to Protein

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The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
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相关实验视频

Updated: Jul 23, 2025

Chemical Triphosphorylation of Oligonucleotides
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三重编码的益生菌RNA氨基化

Meng Su1, Christian Schmitt2, Ziwei Liu1

  • 1MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

Journal of the American Chemical Society
|July 12, 2023
PubMed
概括
此摘要是机器生成的。

在酶之前,RNA可以在没有酶的情况下被选择性氨基基化. 这项研究表明RNA的序列依赖,无酶氨基化,表明RNA受体干中的第二个遗传密码.

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Genetic Incorporation of Biosynthesized L-dihydroxyphenylalanine DOPA and Its Application to Protein Conjugation
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Chemical Triphosphorylation of Oligonucleotides
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Genetic Incorporation of Biosynthesized L-dihydroxyphenylalanine DOPA and Its Application to Protein Conjugation
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科学领域:

  • 生命研究的起源
  • 分子生物学
  • 生物化学

背景情况:

  • 翻译需要氨基酸通过氨基酸-tRNA合成酶连接到tRNA.
  • 在酶进化之前,这种选择性氨基酸的起源是未知的.

研究的目的:

  • 为了研究无酶,依赖序列的RNA氨基化.
  • 探索原始tRNA氨基化过程中的潜在益生菌路径.

主要方法:

  • 对氨基酸-tRNA受体干超悬模仿的两种预生物路径进行了研究.
  • 在氨基化中分析了寡核酸的效率.
  • 从混合无水化供体中检查了氨基化的化学选择性和立体选择性.

主要成果:

  • 已证明无酶,可选择性氨基基化RNA.
  • 过悬的序列对化学选择性的影响很小.
  • 氨基基化选择性取决于RNA干的末端三基对.

结论:

  • 支持RNA受体干内第二个遗传密码的假设.
  • 提供了早期基于RNA的氨基酸激活机制的见解.
  • 这表明了基因编码的起源.