Chen F, MacDonald C C, Wilusz J
UMDNJ-New Jersey Medical School, Department of Microbiology and Molecular Genetics, Newark 07103, USA.
Nucleic Acids Res. 1995 Jul 25;23(14):2614-20. doi: 10.1093/nar/23.14.2614.
Using a series of position and nucleotide variants of the SV40 late polyadenylation signal we have demonstrated that three sequence elements determine the precise site of 3-end cleavage in mammalian pre-mRNAs: an upstream AAUAAA element, a down-stream U-rich element consisting of five nucleotides, at least four of which are uridine, and a nucleotide preference at the site of cleavage in the order A > U > C >> G. Cleavage occurs no closer than 11 bases, but no further than 23 bases from the AAUAAA element. The downstream U-rich element is usually located 10-30 bases from the cleavage site. The relative position of the AAUAAA and the U-rich elements define the approximate region within a 13 base domain in which cleavage will occur. The exact position of cleavage is then determined by the local nucleotide sequence in the order of preference noted above. This model accounts for nearly three quarters of polyadenylation signals surveyed and is consistent with previous experimental observations.
利用一系列SV40晚期聚腺苷酸化信号的位置和核苷酸变体,我们已经证明,三个序列元件决定了哺乳动物前体mRNA 3'端切割的精确位点:一个上游AAUAAA元件、一个由五个核苷酸组成的下游富含U的元件,其中至少四个是尿苷,以及切割位点处的核苷酸偏好顺序为A > U > C >> G。切割发生在距离AAUAAA元件不小于11个碱基但不超过23个碱基的位置。下游富含U的元件通常位于切割位点10 - 30个碱基处。AAUAAA元件和富含U的元件的相对位置定义了一个13个碱基区域内切割将发生的大致区域。然后,切割的确切位置由上述偏好顺序的局部核苷酸序列决定。该模型解释了近四分之三被研究的聚腺苷酸化信号,并且与先前的实验观察结果一致。