Su L K, Kadesch T
Howard Hughes Medical Institute, University of Pennsylvania School of Medicine, Philadelphia 19104-6072.
Mol Cell Biol. 1990 Jun;10(6):2619-24. doi: 10.1128/mcb.10.6.2619-2624.1990.
We demonstrate that the immunoglobulin heavy-chain enhancer functions as the promoter for I mu sterile transcription. The enhancer itself, when placed 5' to the bacterial cat or neo genes, is able to direct transcription by using heterogeneous start sites that are generally the same as those found with bona fide I mu transcripts. In general, promoter activity is dependent on the same sequence motifs important for enhancer activity. However, it appears that a mutation within the conserved octanucleotide ATTTGCAT has a much more severe effect on the promoter activity of the enhancer than the same mutation has on its enhancer activity. This result is consistent with the known role of the octanucleotide as a promoter element, and this is discussed in relation to the biological role of sterile transcription.
我们证明免疫球蛋白重链增强子作为Iμ无菌转录的启动子发挥作用。当增强子自身置于细菌cat或neo基因的5'端时,它能够利用与真正的Iμ转录本通常相同的异质起始位点来指导转录。一般来说,启动子活性依赖于对增强子活性重要的相同序列基序。然而,保守的八聚体ATTTGCAT内的一个突变对增强子启动子活性的影响似乎比对其增强子活性的影响更为严重。这一结果与八聚体作为启动子元件的已知作用一致,并结合无菌转录的生物学作用进行了讨论。