Carswell S, Alwine J C
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia 19104-6076.
Mol Cell Biol. 1989 Oct;9(10):4248-58. doi: 10.1128/mcb.9.10.4248-4258.1989.
The late polyadenylation signal of simian virus 40 functions with greater efficiency than the early polyadenylation signal, in turn affecting steady-state mRNA levels. Two chloramphenicol acetyltransferase (CAT) transient expression vectors, pL-EPA and pL-LPA, that differ only in their polyadenylation signals were constructed by using the early and late polyadenylation signals, respectively. In transfections of Cos, CV-1P, or HeLa cells and subsequent Northern blot analysis of CAT-specific RNA, approximately five times more steady-state CAT mRNA was produced in transfections with pL-LPA than with pL-EPA. The basis for this difference was not related to the specific promoter used or to RNA stability. Overall, the difference in steady-state mRNA levels derived from the two plasmids appeared to be attributable to intrinsic properties of the two polyadenylation signals, resulting in distinctly different cleavage and polyadenylation efficiencies. Additionally, we found that the utilization of the late polyadenylation site was dramatically reduced by deletion of sequences between 48 and 29 nucleotides 5' of the AAUAAA hexanucleotide. This reduction of mRNA levels was shown not to be caused by altered stability of mutant precursor RNAs or mRNAs, suggesting that these upstream sequences constitute an element of the late polyadenylation signal and may cause, at least to some extent, the greater efficiency of utilization of the late polyadenylation site.
猴病毒40的晚期聚腺苷酸化信号比早期聚腺苷酸化信号发挥作用的效率更高,进而影响稳态mRNA水平。通过分别使用早期和晚期聚腺苷酸化信号构建了两个仅在聚腺苷酸化信号上不同的氯霉素乙酰转移酶(CAT)瞬时表达载体,即pL-EPA和pL-LPA。在转染Cos、CV-1P或HeLa细胞并随后对CAT特异性RNA进行Northern印迹分析时,用pL-LPA转染产生的稳态CAT mRNA比用pL-EPA转染产生的大约多五倍。这种差异的基础与所使用的特定启动子或RNA稳定性无关。总体而言,源自这两种质粒的稳态mRNA水平差异似乎归因于这两种聚腺苷酸化信号的内在特性,导致明显不同的切割和聚腺苷酸化效率。此外,我们发现通过缺失六核苷酸AAUAAA 5'端48至29个核苷酸之间的序列,晚期聚腺苷酸化位点的利用率显著降低。mRNA水平的这种降低并非由突变前体RNA或mRNA稳定性的改变引起,这表明这些上游序列构成了晚期聚腺苷酸化信号的一个元件,并且可能至少在一定程度上导致晚期聚腺苷酸化位点更高的利用效率。