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A tail length modifier gene discovered in the Japanese wild mice (Mus musculus molossinus)

A Fujimoto1, N Baba, N Wakasugi

  • 1Laboratory of Animal Genetics, School of Agriculture, Nagoya University, Japan.

Idengaku Zasshi
|April 1, 1991
PubMed

Insights

Researchers investigated t haplotypes in Japanese wild mice. They discovered a new gene, brachyury-interacting tail length modifier (btm), in the MOL-NIS strain that interacts with the T gene to cause taillessness.

Area of Science:

  • Genetics
  • Mammalian Genetics
  • Evolutionary Biology

Background:

  • The t haplotype is a complex of genes on mouse chromosome 17.
  • Certain t haplotypes are associated with male sterility and developmental abnormalities.
  • Investigating t haplotypes in wild mouse populations provides insights into their genetic diversity and evolutionary history.

Purpose of the Study:

  • To determine the presence of t haplotypes in Japanese wild mouse strains (Mus musculus molossinus).
  • To identify genetic factors responsible for taillessness in specific molossinus strains.
  • To characterize a newly identified gene interacting with the T gene.

Main Methods:

  • Cross-breeding experiments between T/+ heterozygous mice and various molossinus strains.
  • Phenotypic analysis of offspring, specifically focusing on tail length and taillessness.
  • Mating experiments to elucidate the genetic basis of the observed traits.

Main Results:

  • Five molossinus strains (MOL-ANJ, MOA, MOL-NEM, MOM, Mns) did not carry the t haplotype, as evidenced by the absence of tailless offspring.
  • A cross involving the MOL-NIS strain produced tailless mice.
  • Taillessness resulted from the interaction between the T gene and a recessive autosomal gene (btm) in the MOL-NIS strain.

Conclusions:

  • The investigated molossinus strains, except MOL-NIS, lack t haplotypes.
  • A novel gene, tentatively named brachyury-interacting tail length modifier (btm), was identified in the MOL-NIS strain.
  • The btm gene's location, whether within or outside the t complex region, requires further investigation.

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