Fitzgerald M, Shenk T
Cell. 1981 Apr;24(1):251-60. doi: 10.1016/0092-8674(81)90521-3.
We have observed three effects of deletion mutations on polyadenylation of late SV40 mRNAs. The first class of mutants lack segments (-3 to -14 bp) between the 5-AAUAAA-3' and normal poly(A) site. These mutants produce mRNas polyadenylated at new sites, downstream from the wild-type site. The poly(A) site is moved farther downstream as the deletions become larger; as a result, polyadenylation always occurs within an 11-19 nucleotide range from the AAUAAA sequence. The second class of mutants lack segments (-12 to -30 bp) between the AAUAAA sequence and the coding region of the mRNA. The poly(A) site for only one of these mutants was studied (dl1457, -12 bp). In this case, the spatial relationship between AAUAAA and poly(A) site is altered. dl1457 produces a class of mRNAs polyadenylated at the first Ca following the AAUAAA sequence, as well as other mRNAs polyadenylated farther downstream. Finally, a 16 bp deletion that includes the AAUAAA sequence prevents poly(A) addition.
我们观察到缺失突变对猴病毒40(SV40)晚期mRNA聚腺苷酸化的三种影响。第一类突变体在5'-AAUAAA-3'与正常聚腺苷酸(poly(A))位点之间缺少片段(-3至-14碱基对)。这些突变体产生在新位点进行聚腺苷酸化的mRNA,这些新位点位于野生型位点的下游。随着缺失片段变大,聚腺苷酸位点会进一步向下游移动;因此,聚腺苷酸化总是在距AAUAAA序列11至19个核苷酸范围内发生。第二类突变体在AAUAAA序列与mRNA编码区之间缺少片段(-12至-30碱基对)。仅对其中一个突变体(dl1457,缺失12碱基对)的聚腺苷酸位点进行了研究。在这种情况下,AAUAAA与聚腺苷酸位点之间的空间关系发生了改变。dl1457产生一类在AAUAAA序列后的第一个胞嘧啶(Ca)处进行聚腺苷酸化的mRNA,以及其他在更下游进行聚腺苷酸化的mRNA。最后,一个包含AAUAAA序列的16碱基对缺失会阻止聚腺苷酸的添加。