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Lethal Alleles02:41

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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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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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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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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

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Recessive AARS1 variants perturb human and mouse development.

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.

HGG Advances
|January 9, 2026
PubMed
Summary
This summary is machine-generated.

Pathogenic alanyl-tRNA synthetase 1 (AARS1) variants cause congenital brain defects. Mouse models confirm AARS1 variants are pathogenic, but early lethality limits detailed neural development studies.

Area of Science:

  • Genetics
  • Developmental Biology
  • Neuroscience

Background:

  • Pathogenic loss-of-function alanyl-tRNA synthetase 1 (AARS1) variants in humans are linked to congenital brain phenotypes, notably microcephaly.
Keywords:
CRISPR-Cas9 mouse modelRNA splicing defectaars1aminoacyl-tRNA-synthetaseembryonic lethalitymicrocephalyneurodevelopmentla disorderpurkinje cell degeneration

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  • The underlying molecular mechanisms remain unclear, though zebrafish aars1 mutants exhibit reduced neurogenesis and increased apoptosis.