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相关概念视频

Gene Conversion02:08

Gene Conversion

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Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
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Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

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Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
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Incomplete Dominance01:43

Incomplete Dominance

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Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
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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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Pleiotropy01:33

Pleiotropy

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Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
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相关实验视频

Updated: May 15, 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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异位基因转换导致定量特征变异

Marina Pfalz1, Seïf-Eddine Naadja1, Jacqui Anne Shykoff1

  • 1Ecologie Société Evolution, CNRS/Université Paris-Saclay/AgroParisTech, Gif-sur-Yvette, France.

Molecular biology and evolution
|April 9, 2025
PubMed
概括
此摘要是机器生成的。

通过平衡选择和宫外基因转换 (EGC) 维持的Arabidopsis防御基因的遗传变异,为健身特征产生多样性. 基因重复的结果EGC是这种变异的关键机制.

关键词:
这就是CRISPR/Cas9的作用.异卵性基因转换异卵性基因转换核酸多态化模式的模式量化遗传变异 量化遗传变异定量特征的位置 (locus).

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Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
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QTL Mapping and CRISPR/Cas9 Editing to Identify a Drug Resistance Gene in Toxoplasma gondii
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QTL Mapping and CRISPR/Cas9 Editing to Identify a Drug Resistance Gene in Toxoplasma gondii

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相关实验视频

Last Updated: May 15, 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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Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
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QTL Mapping and CRISPR/Cas9 Editing to Identify a Drug Resistance Gene in Toxoplasma gondii
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科学领域:

  • 进化遗传学的进化遗传学
  • 植物分子生物学 植物分子生物学
  • 人口遗传学 人口遗传学

背景情况:

  • 自然种群表现出显著的非中性遗传变异.
  • 定量特征位置 (QTLs) 在适应中起着至关重要的作用,但它们的进化机制尚未完全理解.
  • 阿拉比多普西斯的防御代谢物受到遗传变异的影响.

研究的目的:

  • 为了研究一个神秘的QTL的功能和演变,用于Arabidopsis的防御代谢物.
  • 了解在基因家族内产生和维持遗传变异的机制.
  • 探索子宫外基因转换 (EGC) 在产生适应性变异中的作用.

主要方法:

  • 使用CRISPR/Cas9基因编辑来剖析QTL功能.
  • 分析了核酸多态化模式,以推断进化过程.
  • 研究了一个由四个紧密联系的醇-葡萄糖酸O-甲基转移酶基因组成的家族.

主要成果:

  • 在QTL的基础上,鉴定了印-葡萄糖酸盐O-甲基转移酶基因家族内的遗传变异.
  • 观察到平衡选择保持一些遗传变异的证据.
  • 作为变异源的功能分离的基因拷贝之间记录的宫外基因转换 (EGC).

结论:

  • 出于基因复制而产生的异位基因转换 (EGC) 是产生遗传变异的重要机制.
  • 这种变异可以促进自然人群中健身特征的演变.
  • 这项研究提供了关于维护和生成Arabidopsis.遗传多样性的见解.