The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11

Genetics. 2006 Jan;172(1):411-23. doi: 10.1534/genetics.105.047118. Epub 2005 Sep 19.

Abstract

The DDK syndrome is an early embryonic lethal phenotype observed in crosses between females of the DDK inbred mouse strain and many non-DDK males. Lethality results from an incompatibility between a maternal DDK factor and a non-DDK paternal gene, both of which have been mapped to the Ovum mutant (Om) locus on mouse chromosome 11. Here we define a 465-kb candidate interval for the paternal gene by recombinant progeny testing. To further refine the candidate interval we determined whether males from 17 classical and wild-derived inbred strains are interfertile with DDK females. We conclude that the incompatible paternal allele arose in the Mus musculus domesticus lineage and that incompatible strains should share a common haplotype spanning the paternal gene. We tested for association between paternal allele compatibility/incompatibility and 167 genetic variants located in the candidate interval. Two diallelic SNPs, located in the Schlafen gene cluster, are completely predictive of the polar-lethal phenotype. These SNPs also predict the compatible or incompatible status of males of five additional strains.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Cycle Proteins / genetics*
  • Chromosome Mapping
  • Chromosomes / genetics*
  • Crosses, Genetic
  • Female
  • Fertility / genetics*
  • Genes, Lethal*
  • Genetic Linkage
  • Genomic Imprinting / physiology*
  • Haplotypes / genetics
  • Male
  • Mice
  • Mice, Inbred Strains
  • Multigene Family*
  • Phenotype
  • Phylogeny
  • Syndrome

Substances

  • Cell Cycle Proteins
  • schlafen-1 protein, mouse