TY - JOUR
T1 - ISOLATION OF THE MHC GENES ENCODING THE TUMOUR‐SPECIFIC CLASS I ANTIGENS EXPRESSED ON A MURINE FIBROSARCOMA
AU - Stauss, H. J.
AU - Linsk, R.
AU - Fischer, A.
AU - Watts, S.
AU - Banasiak, D.
AU - Haberman, A.
AU - Clark, I.
AU - Forman, J.
AU - McMillan, M.
AU - Schreiber, H.
AU - Goodenow, R. S.
PY - 1986/4
Y1 - 1986/4
N2 - The C3H UV‐induced fibrosarcoma, 1591, is highly immunogenic and, therefore, is readily rejected when transplanted into immunocompetent syngeneic recipients. Previous analysis of 1591 with tumour‐specific or H‐2‐reactive monoclonal antibodies revealed that this antigenicity might be due to the expression of two novel class I major histocompatibility complex (MHC) antigens. In this report we describe the molecular cloning and initial characterization of three genes which account for all of the unique serological class I reactivities observed on this tumour. These include two distinct, but highly conserved, H‐2L‐like genes, and a third gene the product of which bears determinants which are characteristic of both the tumour and of class I products of the H‐2k haplotype. Moreover, each of these genes contains a polymorphic restriction enzyme fragment which is detected in the class I sequences of 1591 relative to normal C3H tissue. Since the expression of these polymorphic class I sequences is relevant to the immunogenicity of 1591, the mutational events by which these genes were generated may be significant to the immunobiology of this tumour.
AB - The C3H UV‐induced fibrosarcoma, 1591, is highly immunogenic and, therefore, is readily rejected when transplanted into immunocompetent syngeneic recipients. Previous analysis of 1591 with tumour‐specific or H‐2‐reactive monoclonal antibodies revealed that this antigenicity might be due to the expression of two novel class I major histocompatibility complex (MHC) antigens. In this report we describe the molecular cloning and initial characterization of three genes which account for all of the unique serological class I reactivities observed on this tumour. These include two distinct, but highly conserved, H‐2L‐like genes, and a third gene the product of which bears determinants which are characteristic of both the tumour and of class I products of the H‐2k haplotype. Moreover, each of these genes contains a polymorphic restriction enzyme fragment which is detected in the class I sequences of 1591 relative to normal C3H tissue. Since the expression of these polymorphic class I sequences is relevant to the immunogenicity of 1591, the mutational events by which these genes were generated may be significant to the immunobiology of this tumour.
UR - http://www.scopus.com/inward/record.url?scp=0022917337&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0022917337&partnerID=8YFLogxK
U2 - 10.1111/j.1744-313X.1986.tb01090.x
DO - 10.1111/j.1744-313X.1986.tb01090.x
M3 - Article
C2 - 2880914
AN - SCOPUS:0022917337
SN - 1744-3121
VL - 13
SP - 101
EP - 112
JO - Journal of Immunogenetics
JF - Journal of Immunogenetics
IS - 2-3
ER -