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相关概念视频

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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The Central Dogma01:25

The Central Dogma

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Overview
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DNA as a Genetic Template02:05

DNA as a Genetic Template

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Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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Gene Duplication and Divergence02:37

Gene Duplication and Divergence

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The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
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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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Initiation of Translation02:33

Initiation of Translation

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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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相关实验视频

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遗传密码的三阶段发展

Tze-Fei Wong1

  • 1Division of Life Science and Applied Genomics Center, Hong Kong University of Science & Technology Hong Kong, China.

Chemical reviews
|August 1, 2024
PubMed
概括

遗传密码最初仅限于20个氨基酸,但由于生物限制而被结. 科学家们现在已经开发了编码新的非正规氨基酸 (ncAAs) 的方法,将遗传字母扩展到其原始限制之外.

科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 进化生物学 进化生物学

背景情况:

  • 标准的遗传密码使用20种氨基酸,分为第一阶段 (前生物可用性) 和第二阶段 (生物合成依赖性).
  • 在进化史的早期,遗传密码被"结",像*Methanopyrus kandleri*这样的生物在数十亿年内没有扩展氨基酸字母.
  • 这种"结"归因于寡生性障碍,在这种情况下,生物高度适应了标准的20个氨基酸,使删除对生存能力有害.

研究的目的:

  • 解释遗传密码"结"状态背后的进化原因.
  • 突出新型非正规氨基酸 (ncAA) 编码方法的发展和成功.
  • 为了强调遗传密码的扩展超出了20种正规的氨基酸.

主要方法:

  • 遗传密码进化和生物适应的历史分析.
  • 对科学发现的回顾解释了遗传密码的"结".
  • 描述允许编码非正规氨基酸 (ncAA) 的方法.

主要成果:

  • 遗传密码最初的20个氨基酸受到前生物的可用性和后来的生物合成的限制.
  • 寡生障碍物防止任何标准氨基酸的去除,保持代码的结构.
  • 科学家们已经成功地设计了编码新型非正规氨基酸 (ncAAs) 的程序,扩大了遗传谱.

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Probing mRNA Kinetics in Space and Time in Escherichia coli using Two-Color Single-Molecule Fluorescence In Situ Hybridization
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结论:

  • 遗传密码的进化轨迹是由环境的可用性和生物适应性形成的.
  • 了解"结"代码的限制为科学创新铺平了道路.
  • 第三阶段非正规氨基酸的成功编码代表了超越传统20种氨基酸的显著扩展.