Ho Y S, Howard A J, Crapo J D
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Am J Respir Cell Mol Biol. 1991 Mar;4(3):278-86. doi: 10.1165/ajrcmb/4.3.278.
The manganese-containing superoxide dismutase (MnSOD) constitutes one of the major cellular defense mechanisms against the toxic effects of superoxide radical. The development of tolerance in adult rats to lethal exposure of O2 (100%) after pre-exposing them to a sublethal concentration of O2 (85%) was found to be closely associated with the increased activity of this enzyme in the lungs. Further experiments have shown that the transcriptional rate of the gene coding for MnSOD in rat lungs is increased at day 3 of 85% O2 exposure. To elucidate the nature of this transcriptional activation during hyperoxic insults, we chose to first understand the structure of the rat MnSOD gene. Three overlapping rat genomic fragments were isolated, and the DNA sequence containing the whole MnSOD gene was completely determined. The rat MnSOD gene contains at least five exons and is located in one piece of 16.4-kb EcoRI genomic DNA fragment. However, Southern blot analysis of total rat genomic DNA probed with MnSOD cDNA revealed an additional hybridizing 8.6-kb EcoRI genomic fragment besides the 16.4-kb one. To clarify the origin of this unexpected hybridizing genomic fragment, three unique genomic sequences derived from the promoter, intron 2, and the 3' untranslated region of the genomic clones were used to rehybridize the same Southern blot filter and were found to only hybridize to the 16.4-kb but not 8.5-kb EcoRI genomic fragment. These data suggest: (1) two MnSOD genes are present per haploid rat genome, and (2) all three cloned genomic fragments are derived from the MnSOD gene, which is located in the 16.4-kb EcoRI genomic fragment.(ABSTRACT TRUNCATED AT 250 WORDS)
含锰超氧化物歧化酶(MnSOD)是细胞抵御超氧阴离子自由基毒性作用的主要防御机制之一。研究发现,成年大鼠在预先暴露于亚致死浓度的氧气(85%)后,对致死性氧气暴露(100%)产生耐受性的过程与肺中该酶活性的增加密切相关。进一步实验表明,在85%氧气暴露的第3天,大鼠肺中编码MnSOD的基因转录速率增加。为了阐明高氧损伤期间这种转录激活的本质,我们选择首先了解大鼠MnSOD基因的结构。分离出三个重叠的大鼠基因组片段,并完全确定了包含整个MnSOD基因的DNA序列。大鼠MnSOD基因至少包含五个外显子,位于一条16.4 kb的EcoRI基因组DNA片段中。然而,用MnSOD cDNA探测大鼠总基因组DNA的Southern印迹分析显示,除了16.4 kb的片段外,还有一个额外的8.6 kb EcoRI基因组杂交片段。为了阐明这个意外杂交基因组片段的来源,使用了来自基因组克隆的启动子、内含子2和3'非翻译区的三个独特基因组序列对同一Southern印迹滤膜进行再杂交,发现它们仅与16.4 kb而不是8.5 kb的EcoRI基因组片段杂交。这些数据表明:(1)单倍体大鼠基因组中存在两个MnSOD基因;(2)所有三个克隆的基因组片段均来自位于16.4 kb EcoRI基因组片段中的MnSOD基因。(摘要截短于250字)