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相关概念视频

The Eukaryotic Promoter Region02:40

The Eukaryotic Promoter Region

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The eukaryotic promoter region is a segment of DNA located upstream of a gene. It contains an RNA polymerase binding site, a transcription start site, and several cis-regulatory sequences.  The proximal promoter region is located in the vicinity of the gene and has cis-regulatory sequences and the core promoter. The core promoter is the binding site for RNA polymerase and is usually located between -35 and +35 nucleotides from the transcription start site. The distal promoter regions are...
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Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
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Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
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In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
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相关实验视频

Updated: Jun 19, 2025

A Customizable Protocol for String Assembly gRNA Cloning STAgR
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生成信息密集的促销器序列,具有最佳的字符串包装.

Virgile Andreani1,2, Eric J South2,3, Mary J Dunlop1,2,3

  • 1Biomedical Engineering Department, Boston University, Boston, Massachusetts, United States of America.

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概括
此摘要是机器生成的。

设计具有重叠结合位点的核酸序列是具有挑战性的. 这种新的计算方法有效地创建了密集的DNA数组,可以证明多个结合点的最佳包装.

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Transient Gene Expression in Tobacco using Gibson Assembly and the Gene Gun
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Generation of Plasmid Vectors Expressing FLAG-tagged Proteins Under the Regulation of Human Elongation Factor-1&#945; Promoter Using Gibson Assembly
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Generation of Plasmid Vectors Expressing FLAG-tagged Proteins Under the Regulation of Human Elongation Factor-1α Promoter Using Gibson Assembly

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科学领域:

  • 计算生物学 计算生物学
  • 合成生物学 合成生物学
  • 生物信息学是一种生物信息学.

背景情况:

  • 自然促进器区域包含重叠的转录因子结合位,调节转录启动.
  • 设计具有密集,重叠结合点的核酸序列是分子生物学中的一个重大挑战.

研究的目的:

  • 为了应对设计具有密集,重叠结合点的核酸序列的挑战.
  • 开发一种计算技术,有效地将DNA-蛋白质结合点组装成连续的DNA延伸.

主要方法:

  • 核酸串包装问题 (SPP) 被确定为一个NP-hard问题.
  • 该SPP被简化为一个定向问题与整数距离.
  • 现代的整数线性编程解决方案被用来找到最佳解决方案.

主要成果:

  • 该方法在0.05-10秒内最佳地将20-100个结合点包装成50-300个基对DNA数组.
  • 该方法保证了可证明的最佳解决方案,优于近似算法.
  • 该方法可以控制结合点的频率,并可以结合固定的序列元素来设计特定的元素,如细菌促进剂.

结论:

  • 提出的核酸串包装方法加速了具有复杂DNA-蛋白相互作用的序列的设计.
  • 这一策略可以帮助探讨复杂的结合点安排如何影响基因表达和生物分子机制.
  • 与合成和查的整合可以促进对基因调节和细胞功能的理解.