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相关概念视频

Lethal Alleles02:41

Lethal Alleles

15.6K
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
15.6K
Mutations01:39

Mutations

83.8K
Overview
83.8K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.0K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.0K
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

11.6K
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
11.6K
Incomplete Dominance01:43

Incomplete Dominance

22.9K
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.
22.9K
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

14.0K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
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相关实验视频

Updated: Jul 25, 2025

Shifting Zebrafish Lethal Skeletal Mutant Penetrance by Progeny Testing
08:39

Shifting Zebrafish Lethal Skeletal Mutant Penetrance by Progeny Testing

Published on: September 1, 2017

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摘要:很少有新的突变是衰退的致命的致命的.

Benjamin R Epley1

  • 1Ecology and Evolution, University of Chicago, Chicago, IL, United States.

Evolution; international journal of organic evolution
|June 24, 2023
PubMed
概括

在人类和果中,不到1%的新突变是衰退致命的. 目前的方法难以准确估计这些致命突变的比例,这影响了遗传研究.

科学领域:

  • 遗传学 是一个遗传学.
  • 进化生物学 进化生物学
  • 人口遗传学 人口遗传学

背景情况:

  • 了解新突变的影响对于进化和遗传学研究至关重要.
  • 递归致命突变可以显著影响种群遗传学,但难以检测.

研究的目的:

  • 为了确定人类和Drosophila melanogaster的衰减致命突变的频率.
  • 评估网站频谱 (SFS) 方法在估计衰退致命突变中的准确性.

主要方法:

  • 对人类和Drosophila melanogaster种群中非同义突变的分析.
  • 将突变数据与场地频谱 (SFS) 分析进行比较.

主要成果:

  • 不到1%的非同义突变被确定为衰退性致死性.
  • 基于SFS的标准方法不准确地估计了衰退致命突变的比例,尽管它们对于非致命的健身效应具有强度.

结论:

  • 衰退性致死性是突变动态的一个罕见但重要的因素.
  • 需要新的方法来准确量化衰退致命突变,以获得强大的人口遗传推断.

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Removal of an Internal Translational Start Site from mRNA While Retaining Expression of the Full-Length Protein
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