TY - JOUR
T1 - Comparison of the promoter regions of H-2K and H-2Kbm1 class I MHC genes
AU - Ozawa, Kazuo
AU - Saka, Fujiko
AU - Kitabayashi, Issay
AU - Lmai, Takashi
AU - Soeda, Eiichi
AU - Israel, Alain
AU - Gachelin, Gabriel
AU - Yokoyama, Kazushige
PY - 1990/7/25
Y1 - 1990/7/25
N2 - The 2.0 kb-long nucleotide sequences of the promoter regions of two closely related class I genes of the mouse major histocompatibility complex (H-2Kb and H-2Kbm1) have been determined and compared. The promoter sequence of the H-2Kbm1 gene differs from that of the H-2Kb gene by a single deletion of a 'C' at position -456 in the upstream region of H-2Kbm1 gene. The actual existence of this deletion of a single base in genomic DNA has been verified by genomic DNA hybridization, using oligonucleotide probes specific for H-2Kbm1 or H-2Kb respectively. The effect on the enhancer activity of H-2Kbm1 promoter region of the difference at position -456 has been analyzed by the chloramphenicol acetyltransferase (CAT) assay, using appropriate Ddel fragments (-533 to -408 for H-2Kbm1; - 534 to - 408 for H-2Kb) cloned downstream of pH-2(367)CAT gene construct. The CAT activity determined by the H-2Kbm1 fragment was about 3-fold higher than that of H-2Kb, a result which probably accounts for the higher level of the H-2Kbm1 transcript and antigen in lymph node cells.
AB - The 2.0 kb-long nucleotide sequences of the promoter regions of two closely related class I genes of the mouse major histocompatibility complex (H-2Kb and H-2Kbm1) have been determined and compared. The promoter sequence of the H-2Kbm1 gene differs from that of the H-2Kb gene by a single deletion of a 'C' at position -456 in the upstream region of H-2Kbm1 gene. The actual existence of this deletion of a single base in genomic DNA has been verified by genomic DNA hybridization, using oligonucleotide probes specific for H-2Kbm1 or H-2Kb respectively. The effect on the enhancer activity of H-2Kbm1 promoter region of the difference at position -456 has been analyzed by the chloramphenicol acetyltransferase (CAT) assay, using appropriate Ddel fragments (-533 to -408 for H-2Kbm1; - 534 to - 408 for H-2Kb) cloned downstream of pH-2(367)CAT gene construct. The CAT activity determined by the H-2Kbm1 fragment was about 3-fold higher than that of H-2Kb, a result which probably accounts for the higher level of the H-2Kbm1 transcript and antigen in lymph node cells.
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U2 - 10.1093/nar/18.14.4185
DO - 10.1093/nar/18.14.4185
M3 - Article
C2 - 2377459
AN - SCOPUS:0025293897
SN - 0305-1048
VL - 18
SP - 4185
EP - 4190
JO - Nucleic acids research
JF - Nucleic acids research
IS - 14
ER -