CSIRO Division of Plant Industry, GPO Box 1600, Canberra, ACT 2601, Australia.
EMBO J. 1987 Nov;6(11):3203-8. doi: 10.1002/j.1460-2075.1987.tb02636.x.
A 176 bp DNA sequence lying upstream of the octopine synthase (ocs) promoter, previously shown to have enhancer-like properties in transgenic tobacco [Ellis et al. (1987) EMBO J., 6, 11-16], functions as an enhancer in protoplasts of Zea mays (a monocot plant) and Nicotiana plumbaginifolia (a dicotplant). We have characterized this element by transient expression assays using a linked alcohol dehydrogenase (Adh1) promoter from Z. mays and the chloramphenicol acetyltransferase coding sequences. The ocs sequence functions in both orientations but its enhancing activity is dependent upon its distance from the Adh1 promoter. Transient expression assays using deletion mutants and synthetic oligonucleotides show that a 16 bp palindrome ACGTAAGCGCTTACGT, contained within the 176 bp fragment, is essential and sufficient for enhancing activity in transient expression assays.
一段位于章鱼碱合酶(ocs)启动子上游的 176 个碱基对的 DNA 序列,先前已被证明在转基因烟草中具有增强子样性质[Ellis 等人(1987)EMBO J.,6,11-16],在玉米(单子叶植物)和烟草(双子叶植物)原生质体中作为增强子发挥作用。我们使用来自玉米的连接的醇脱氢酶(Adh1)启动子和氯霉素乙酰转移酶编码序列通过瞬时表达测定来表征该元件。ocs 序列以两种取向起作用,但其增强活性取决于其与 Adh1 启动子的距离。使用缺失突变体和合成寡核苷酸的瞬时表达测定表明,176 个碱基对片段中包含的 16 个碱基对回文 ACGTAAGCGCTTACGT 对于瞬时表达测定中的增强活性是必需且充分的。