Fu H, Kim S Y, Park W D
Department of Biochemistry and Biophysics, Texas A & M University, College Station 77843-2128, USA.
Plant Cell. 1995 Sep;7(9):1387-94. doi: 10.1105/tpc.7.9.1387.
The 3.6 kb of 5' flanking sequence, leader intron, and 0.7 kb of 3' sequence from the potato sucrose synthase gene Sus4-16 are sufficient to direct high-level expression in developing tubers, in basal tissues of axillary buds and shoots, and in meristems and caps of roots, and to confer sucrose inducibility in leaves. By examining a series of deletion and substitution constructs in transgenic potato plants, we found that this pattern of expression requires 5' flanking sequences both upstream and downstream of position -1500 and that sequences between positions -1500 and -267 are essential for sucrose induction. Replacement of the native 3' sequence with the nopaline synthase 3' sequence resulted in the loss of sucrose inducibility and of expression in basal tissues of axillary buds. A general decrease in expression in other tissues was also observed. Removal of the 1612-bp leader intron also had a dramatic effect on both the pattern and level of expression.
来自马铃薯蔗糖合酶基因Sus4-16的3.6 kb 5'侧翼序列、前导内含子和0.7 kb 3'序列足以在发育中的块茎、腋芽和茎的基部组织、根的分生组织和根尖中指导高水平表达,并赋予叶片蔗糖诱导性。通过检测转基因马铃薯植株中的一系列缺失和替换构建体,我们发现这种表达模式需要-1500位点上游和下游的5'侧翼序列,并且-1500和-267位点之间的序列对于蔗糖诱导至关重要。用胭脂碱合酶3'序列替换天然3'序列导致蔗糖诱导性丧失以及腋芽基部组织中的表达丧失。在其他组织中也观察到表达普遍下降。去除1612 bp的前导内含子对表达模式和水平也有显著影响。