Ott R W, Hansen L K
Department of Biology, Boise State University, Idaho 83725, USA.
Mol Gen Genet. 1996 Oct 16;252(5):563-71. doi: 10.1007/BF02172402.
Sixteen segments of Arabidopsis thaliana DNA that function as enhancers in transgenic tobacco plants were isolated using the pROA97 enhancer cloning vehicle and library transformation of Nicotiana tabacum. The sequences were compared for AT content, homology, repeated motifs, and expression pattern in transgenic N. tabacum. The sequences were average with respect to the AT content of A. thaliana DNA. They could be placed into seven homology groups. Five of the sequences are single-copy sequences. The remaining eleven sequences represent two homology groups. Homology Group I contains seven sequences with minor differences. Homology Group II contains four sequences with minor differences. Two repeated motifs were identified (5'-CCTCT-3' and 5'-AAGGAT-3'). Both repeated motifs are found in other plant enhancers, and in the promoter region of the cauliflower mosaic virus 35S gene. In the 35S gene TATA region, the motifs can form two alternative stem-loop structures. The TATATAA sequence is located in the loop region of both stem-loop structures.
利用pROA97增强子克隆载体和烟草文库转化技术,从拟南芥中分离出16个在转基因烟草植株中起增强子作用的DNA片段。对这些序列的AT含量、同源性、重复基序以及在转基因烟草中的表达模式进行了比较。这些序列的AT含量与拟南芥DNA的平均水平相当。它们可被分为七个同源组。其中五个序列为单拷贝序列。其余十一个序列代表两个同源组。同源组I包含七个差异较小的序列。同源组II包含四个差异较小的序列。鉴定出两个重复基序(5'-CCTCT-3'和5'-AAGGAT-3')。这两个重复基序在其他植物增强子以及花椰菜花叶病毒35S基因的启动子区域中均有发现。在35S基因的TATA区域,这些基序可形成两种不同的茎环结构。TATATAA序列位于两种茎环结构的环区域内。