Rothnie H M, Reid J, Hohn T
Friedrich Miescher Institute, Basel, Switzerland.
EMBO J. 1994 May 1;13(9):2200-10. doi: 10.1002/j.1460-2075.1994.tb06497.x.
The requirement for sequence specificity in the AAUAAA motif of the cauliflower mosaic virus (CaMV) polyadenylation signal was examined by saturation mutagenesis. While deletion of AAUAAA almost abolished processing at the CaMV polyadenylation site, none of the 18 possible single base mutations had a dramatic effect on processing efficiency. The effect of replacing all six nucleotides simultaneously varied depending on the sequence used, but some replacements were as detrimental as the deletion mutant. Taken together, these results confirm that AAUAAA is an essential component of the CaMV polyadenylation signal, but indicate that a high degree of sequence variation can be tolerated. A repeated UUUGUA motif was identified as an important upstream accessory element of the CaMV polyadenylation signal. This sequence was able to induce processing at a heterologous polyadenylation site in a sequence-specific and additive manner. The effect of altering the spacing between this upstream element and the AAUAAA was examined; moving these two elements closer together or further apart reduces the processing efficiency. The upstream element does not function to signal processing at the CaMV polyadenylation site if placed downstream of the cleavage site. Analysis of further upstream sequences revealed that almost all of the 200 nt fragment required for maximal processing contributes positively to processing efficiency. Furthermore, isolated far upstream sequences distinct from UUUGUA were also able to induce processing at a heterologous polyadenylation site.
通过饱和诱变研究了花椰菜花叶病毒(CaMV)聚腺苷酸化信号的AAUAAA基序对序列特异性的要求。虽然删除AAUAAA几乎消除了CaMV聚腺苷酸化位点的加工,但18种可能的单碱基突变中没有一种对加工效率有显著影响。同时替换所有六个核苷酸的效果因所用序列而异,但一些替换与缺失突变体一样有害。综合这些结果证实,AAUAAA是CaMV聚腺苷酸化信号的重要组成部分,但表明可以容忍高度的序列变异。一个重复的UUUGUA基序被确定为CaMV聚腺苷酸化信号的重要上游辅助元件。该序列能够以序列特异性和累加的方式在异源聚腺苷酸化位点诱导加工。研究了改变该上游元件与AAUAAA之间间距的影响;将这两个元件移近或移远会降低加工效率。如果将上游元件置于切割位点下游,则它不能在CaMV聚腺苷酸化位点发出加工信号。对更远上游序列的分析表明,最大加工所需的几乎所有200 nt片段都对加工效率有正向贡献。此外,与UUUGUA不同的分离的远上游序列也能够在异源聚腺苷酸化位点诱导加工。