Mulder Harm J, Nikolaev Igor, Madrid Susan M
Danisco Innovation Copenhagen, Langebrogade 1, DK 1001 Copenhagen, Denmark.
Fungal Genet Biol. 2006 Aug;43(8):560-72. doi: 10.1016/j.fgb.2006.02.005. Epub 2006 May 18.
The promoters of UPR target genes contain an unfolded protein response element (UPRE), which confers the stress inducibility to the gene, via an interaction with the transcription activator HACA. In the promoters of the Aspergillus ER-stress responsive genes bipA, cypB, pdiA, prpA, tigA, and hacA, a consensus sequence was identified, which was located close to the transcription start site of the gene (<81 bp), and corresponds to the sequence CAN(G/A)NTGT/GCCT. The UPRE is a partly palindromic sequence around a dispensable spacer nucleotide, followed by four highly conserved bases. By an in vitro selection procedure, an optimal binding site for HACA was isolated. This sequence, ACACGTGTCCT, resembles the UPRE but lacks the spacer nucleotide. It has a much higher binding affinity than the identified UPREs, and in vivo it behaves as a more powerful cis-acting element.
未折叠蛋白反应(UPR)靶基因的启动子含有一个未折叠蛋白反应元件(UPRE),该元件通过与转录激活因子HACA相互作用赋予基因应激诱导性。在曲霉内质网应激反应基因bipA、cypB、pdiA、prpA、tigA和hacA的启动子中,鉴定出一个共有序列,该序列位于基因转录起始位点附近(<81 bp),对应序列为CAN(G/A)NTGT/GCCT。UPRE是围绕一个可有可无的间隔核苷酸的部分回文序列,后面跟着四个高度保守的碱基。通过体外筛选程序,分离出了HACA的最佳结合位点。该序列ACACGTGTCCT与UPRE相似,但缺少间隔核苷酸。它比已鉴定的UPREs具有更高的结合亲和力,并且在体内它表现为一个更强有力的顺式作用元件。