Guerineau F, Brooks L, Mullineaux P
John Innes Institute, AFRC Institute of Plant Science Research, Norwich, UK.
Mol Gen Genet. 1991 Apr;226(1-2):141-4. doi: 10.1007/BF00273597.
Deletions were made in the cauliflower mosaic virus polyadenylation sequence which was cloned downstream of the beta-glucuronidase gene (gus). The populations of mRNAs generated in tobacco mesophyll protoplasts by transient expression with the various constructs were analysed using a polymerase chain reaction procedure. When no deletion was present in the sequence, the mRNA appeared to be polyadenylated at two major polyadenylation sites. A deletion upstream from the AATAAA sequence made the population of polyadenylated mRNAs very heterogenous at their 3' ends. A deletion downstream of the AATAAA sequence had no effect on the choice of the site. Alternative polyadenylation sites were used when the native polyadenylation site was deleted. These results are discussed in relation to data obtained with other polyadenylation sequences from both plants and animals.
对克隆于β-葡萄糖醛酸酶基因(gus)下游的花椰菜花叶病毒多聚腺苷酸化序列进行了缺失操作。使用聚合酶链反应程序分析了用各种构建体在烟草叶肉原生质体中瞬时表达产生的mRNA群体。当序列中不存在缺失时,mRNA似乎在两个主要的多聚腺苷酸化位点进行多聚腺苷酸化。AATAAA序列上游的缺失使得多聚腺苷酸化mRNA群体在其3'末端非常异质。AATAAA序列下游的缺失对位点选择没有影响。当天然多聚腺苷酸化位点缺失时,使用了替代的多聚腺苷酸化位点。结合从植物和动物的其他多聚腺苷酸化序列获得的数据对这些结果进行了讨论。