Scottish Crop Research Institute, DD2 5DA, Invergowrie, Dundee, Scotland, UK.
Plant Cell Rep. 1994 Sep;13(12):703-8. doi: 10.1007/BF00231628.
Plasmids containing various fragments of the β-glucuronidase (GUS) gene were placed in antisense orientation downstream of the cauliflower mosaic virus 35S promoter and cotransfected with a 35S-gus construct into tobacco mesophyll protoplasts. None of the partial-length sequences were as effective as the full-length sequence in reducing GUS activity. The presence of a polyadenylation sequence downstream of the antisense sequence had an enhancing effect. The activity of the antisense sequence was largely affected by the incubation temperature of the transfected protoplasts. The chloramphenicol acetyltransferase (CAT) gene was fused to the gus coding sequence. When this construct was cotransfected with an antisense sequence directed against CAT, GUS activity was reduced. The implications of these results for the design and uses of antisense sequences are discussed.
将含有β-葡萄糖醛酸酶(GUS)基因各种片段的质粒置于花椰菜花叶病毒 35S 启动子的反义方向下游,并与 35S-gus 构建体共转染入烟草叶肉原生质体。在降低 GUS 活性方面,没有一个部分序列像全长序列那样有效。反义序列下游的聚腺苷酸化序列具有增强作用。反义序列的活性在很大程度上受转染原生质体的孵育温度的影响。氯霉素乙酰转移酶(CAT)基因与 gus 编码序列融合。当该构建体与针对 CAT 的反义序列共转染时,GUS 活性降低。这些结果对反义序列的设计和应用具有重要意义。