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相关概念视频

Epistasis Analysis01:09

Epistasis Analysis

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Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
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Epistasis01:39

Epistasis

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In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
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Multiple Allele Traits01:49

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The Concept of Multiple Allelism
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Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
9.9K
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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Exon Recombination02:32

Exon Recombination

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The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
Exon shuffling follows “splice frame rules.” Each exon...
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相关实验视频

Updated: Jun 9, 2025

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
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An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

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在Pol II触发环哈普洛类型中的更高阶表观.

Bingbing Duan1, Chenxi Qiu2, Steve W Lockless3

  • 1Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.

Genetics
|October 24, 2024
PubMed
概括
此摘要是机器生成的。

RNA聚合酶II的触发环 (TL) 控制着转录. 不兼容的物种特异性TL相互作用揭示了复杂的遗传表现,为这种关键蛋白质域如何演变提供了见解.

关键词:
深度突变扫描 (deep mutational scanning) 是一种对突变进行深度扫描的方法.史诗主义就是一种史诗主义.单质类型的单质类型这是一个触发环.

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CRISPR-Mediated Reorganization of Chromatin Loop Structure
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相关实验视频

Last Updated: Jun 9, 2025

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
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An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

Published on: November 3, 2010

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Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events
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CRISPR-Mediated Reorganization of Chromatin Loop Structure
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CRISPR-Mediated Reorganization of Chromatin Loop Structure

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科学领域:

  • 分子生物学分子生物学
  • 遗传学 遗传学 是一个
  • 生物化学 生物化学

背景情况:

  • RNA聚合酶II (Pol II) 对于基因转录至关重要.
  • 保护的触发回路 (TL) 域的Pol II调节转录保真性和速度.
  • 之前的研究探讨了在TL和周围的双对基因相互作用.

研究的目的:

  • 了解在Pol II TL中的功能残留物相互作用.
  • 研究个体突变如何影响TL功能.
  • 在多重替代TLs中剖析更高阶遗传相互作用的性质.

主要方法:

  • 在TL残留物之间对对基因相互作用的分析.
  • 在Saccharomyces cerevisiae Pol II.中构建和测试多次置换的TLs.
  • 检查TL残留物与更广泛的Pol II蛋白之间的表观性.

主要成果:

  • 在S. cerevisiae Pol II背景下,鉴定了异种物种TL之间的广泛不兼容性.
  • 在TL残留物中揭示了复杂的,更高阶的表观症,包括积极和消极的相互作用.
  • 证明了一些表观性模式仅从中间基因型中显现出来.

结论:

  • 在Pol II TL及其周围的物种特异性相互作用至关重要.
  • 高级表观症在塑造TL功能和进化方面发挥着重要作用.
  • 特定的TL残留物表现出明显的表观性模式,可能指导TL演变.