Boss J M, Strominger J L
Proc Natl Acad Sci U S A. 1986 Dec;83(23):9139-43. doi: 10.1073/pnas.83.23.9139.
To investigate the cis-acting DNA elements that are involved in regulation of class II major histocompatibility complex genes, including gamma-interferon (gamma-IFN) induction, 5' flanking DNA deletions of a DQ beta "minigene" were analyzed in stable transfected cell lines. At least four elements 5' to the gene were found to be involved in DQ beta regulation. Deletion of sequences from -2500 to -159 base pairs (bp) resulted in increased transcription, suggesting that negative regulatory elements resided in the deleted region. These clones were all capable of responding to gamma-IFN. Further deletion of sequences from -159 to -128 bp resulted in constitutive high level transcription and the inability of these constructions to respond to gamma-IFN. A deletion to -107 bp resulted in a decrease in the basal level of expression that was restored by removal of the 5' DNA sequence to -82 bp, suggesting the presence of a second negative element. Finally, deletion to -64 bp caused a marked decrease in expression, suggesting the loss of an element necessary for high levels of transcription. The gamma-IFN control and the transcription control elements contain the conserved upstream sequences found in all class II genes, suggesting a role for these sequences.
为了研究参与调控II类主要组织相容性复合体基因的顺式作用DNA元件,包括γ干扰素(γ-IFN)诱导作用,我们在稳定转染的细胞系中分析了一个DQβ“小基因”的5'侧翼DNA缺失情况。发现基因5'端至少有四个元件参与DQβ的调控。缺失从-2500到-159碱基对(bp)的序列导致转录增加,这表明负调控元件存在于缺失区域。这些克隆都能够对γ-IFN作出反应。进一步缺失从-159到-128 bp的序列导致组成型高水平转录,并且这些构建体无法对γ-IFN作出反应。缺失到-107 bp导致基础表达水平下降,而通过将5' DNA序列去除到-82 bp可恢复该水平,这表明存在第二个负元件。最后,缺失到-64 bp导致表达显著下降,这表明缺失了高水平转录所需的一个元件。γ-IFN控制元件和转录控制元件包含在所有II类基因中发现的保守上游序列,这表明了这些序列的作用。