Eisermann A, Tiller K, Link G
University of Bochum, Plant Cell Physiology and Molecular Biology, FRG.
EMBO J. 1990 Dec;9(12):3981-7. doi: 10.1002/j.1460-2075.1990.tb07619.x.
The psbA gene which is differentially expressed in vivo in chloroplasts and etioplasts has an unusual promoter, containing both prokaryotic-type '-35' and '-10' elements and a sequence motif that resembles the nuclear TATA box. Single base pair substitutions were introduced into the mustard psbA promoter and the mutants were tested in transcription and DNA binding experiments, using extracts from either chloroplasts or etioplasts. Positions within the '-35' region appear to play an essential role in the chloroplast but not in the etioplast system. Altering the first or second position of the 'TATA box'-like region led to decreased psbA in vitro transcription in either plastid extract. These two mutations, however, did not affect binding of extracts to the (linear) psbA promoter fragment in gel retardation assays. Fragments carrying two other plastid promoters effectively competed psbA promoter binding of the etioplast extract, but more weakly that of the chloroplast extract. Lambda exonuclease mapping shows that the 5' border of the binding region is more upstream with the etioplast than with the chloroplast system, whereas the 3' border appears to be the same. Hence, protein(s) of the two plastid types seem to interact differently with the mustard psbA promoter in vitro and perhaps also in vivo.
在叶绿体和黄化质体中体内差异表达的psbA基因具有一个不同寻常的启动子,它包含原核生物类型的“-35”和“-10”元件以及一个类似于核TATA框的序列基序。将单碱基对替换引入芥菜psbA启动子中,并使用来自叶绿体或黄化质体的提取物在转录和DNA结合实验中对突变体进行测试。“-35”区域内的位置似乎在叶绿体系统中起重要作用,而在黄化质体系统中则不然。改变“TATA框”样区域的第一个或第二个位置会导致在任何一种质体提取物中psbA体外转录减少。然而,这两个突变在凝胶阻滞试验中并不影响提取物与(线性)psbA启动子片段的结合。携带另外两个质体启动子的片段有效地竞争了黄化质体提取物对psbA启动子的结合,但对叶绿体提取物的竞争较弱。λ外切核酸酶图谱显示,与叶绿体系统相比,黄化质体结合区域的5'边界更靠上游,而3'边界似乎相同。因此,两种质体类型的蛋白质在体外以及可能在体内与芥菜psbA启动子的相互作用似乎有所不同。