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Genome Biology20023:spotlight-20020805-01

  • Published:


  • Cell Mass
  • Choice Model
  • Homozygous Mutation
  • Inner Cell Mass
  • Online Publication

X-chromosome inactivation (XCI) is controlled by expression of the Tsix gene and its regulation of Xist mRNA accumulation. Deleting one copy of Tsix results in skewed XCI towards the mutated X chromosome in female soma. In an Advanced Online Publication in Nature Genetics, Jeannie Lee reports the generation of homozygous Tsix-null mice by breeding heterozygote animals (Nature Genetics, 29 July 2002, doi:10.1038/ng939). The frequency of homozygote offspring was 20-40% of that expected. Furthermore, homozygous mutation caused a significant sex-ratio distortion favouring male births. Homozygous null females had extremely low fertility and were often sterile. The sex-ratio distortion seems to be linked to female-specific defects in trophoblast and inner cell mass (ICM) growth. Lee generated hybrid mice with polymorphic X chromosomes to monitor XCI. She demonstrated that the loss of both copies of Tsixrandomizes XCI. Lee proposes a "chaotic" choice model to explain these observations.


  1. Tsix, a gene antisense to Xist at the X-inactivation centre.Google Scholar
  2. Targeted mutagenesis of Tsix leads to nonrandom X inactivation.Google Scholar
  3. Nature Genetics, []


© BioMed Central Ltd 2002