A quantitative trait locus in major histocompatibility complex determining latent period of mouse lymphomas

Jpn J Cancer Res. 1996 Apr;87(4):401-4. doi: 10.1111/j.1349-7006.1996.tb00236.x.

Abstract

The effects of two host genes on retrovirus-induced murine lymphoma were evaluated by studying 114 F2 intercross mice between SL/Kh and AKR/Ms mice. Out of 47 T-lymphoma-bearing F2 mice, 45 had the AKR-derived dominant allele at Tism-1. The length of the lymphoma latent period was not related to type of tumor. Instead, it was significantly shortened by a recessive SL/Kh-derived allele at a major histocompatibility complex (MHC)-linked locus on Chr. 17. A quantitative trait analysis of the latent period yielded a maximal logarithm of likelihood ratio for linkage (LOD) score of 7.06 at a class II gene within MHC. The SL/Kh-derived recessive gene was named lla (lymphoma latency acceleration).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • DNA, Satellite / genetics
  • Genetic Linkage
  • Genotype
  • Histocompatibility Antigens Class II / genetics*
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, B-Cell / immunology*
  • Lymphoma, T-Cell / genetics*
  • Lymphoma, T-Cell / immunology*
  • Mice
  • Mice, Inbred Strains
  • Polymorphism, Genetic

Substances

  • DNA, Satellite
  • Histocompatibility Antigens Class II