Ozawa K, Saka F, Kitabayashi I, Imai T, Soeda E, Israel A, Gachelin G, Yokoyama K
Gene Bank, Life Science Tsukuba Research Center, RIKEN, Institute of Physical and Chemical Research, Ibaraki, Japan.
Nucleic Acids Res. 1990 Jul 25;18(14):4185-90. doi: 10.1093/nar/18.14.4185.
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 DdeI 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.
已测定并比较了小鼠主要组织相容性复合体两个密切相关的I类基因(H-2Kb和H-2Kbm1)启动子区域2.0 kb长的核苷酸序列。H-2Kbm1基因的启动子序列与H-2Kb基因的启动子序列不同,在H-2Kbm1基因上游区域的-456位有一个“C”的单碱基缺失。通过分别使用针对H-2Kbm1或H-2Kb的寡核苷酸探针进行基因组DNA杂交,已证实基因组DNA中这种单碱基缺失的实际存在。通过氯霉素乙酰转移酶(CAT)测定法,使用克隆在pH-2(367)CAT基因构建体下游的合适DdeI片段(H-2Kbm1为-533至-408;H-2Kb为-534至-408),分析了-456位差异对H-2Kbm1启动子区域增强子活性的影响。由H-2Kbm1片段测定的CAT活性比H-2Kb的高约3倍,这一结果可能解释了淋巴结细胞中H-2Kbm1转录本和抗原的较高水平。