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Lethal Alleles02:41

Lethal Alleles

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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...
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Pedigree Analysis01:35

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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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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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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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Updated: Jan 13, 2026

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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衰退的AARS1变种扰乱了人类和小鼠的发育.

Jennifer L Watts1, Nicole Costantino1, Ammar Husami2

  • 1Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, 43215, USA.

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概括
此摘要是机器生成的。

致病性阿兰-tRNA合成酶1 (AARS1) 变体导致先天性脑缺陷. 鼠标模型证实AARS1变种具有致病性,但早期死亡率限制了详细的神经发育研究.

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科学领域:

  • 遗传学 是一个遗传学.
  • 发展生物学 发展生物学
  • 神经科学是一个神经科学.

背景情况:

  • 人类中的致病性功能丧失的alanyl-tRNA合成酶1 (AARS1) 变体与先天性大脑表型有关,特别是小头症.
  • 底层的分子机制仍然不清楚,尽管斑马鱼aars1突变体表现出减少的神经发生和增加亡.

研究的目的:

  • 用小鼠模型研究Aars1在胚胎大脑发育中的作用.
  • 确认已识别的人类AARS1变异的致病性.

主要方法:

  • 创建和分析两个具有明显Aars1等位基因 (missense和indel) 的小鼠模型.
  • 在体外拼接测试以评估变异效应.
  • 对异和同鼠的表型分析,包括普金尼细胞评估和运动协调测试.

主要成果:

  • 对于missense或indel Aars1等位基因的同卵性小鼠,表现出早期的胚胎致死性.
  • Aars1G80S/wt异合的小鼠显示普金氏细胞免疫活性降低,但没有大脑小脑异常或运动缺陷.
  • 实验室试验证实了人类AARS1等位基因的致病性.

结论:

  • 这项研究证实,AARS1中的致病基因对小鼠的胚胎死亡率有所贡献.
  • 虽然异卵性小鼠显示微妙的神经元变化,但同卵性模型的早期死亡率阻止了对Aars1在神经发育中的作用的全面调查.