Fu X Y, Ge H, Manley J L
Department of Biological Sciences, Columbia University, New York, NY 10027.
EMBO J. 1988 Mar;7(3):809-17. doi: 10.1002/j.1460-2075.1988.tb02879.x.
We have studied the role in pre-mRNA splicing of the nucleotide sequence preceding the SV40 early region 3' splice site. Somewhat surprisingly, neither the pyrimidine at the highly conserved -3 position, nor the polypyrimidine stretch that extends from -5 to -15, relative to the 3' splice site, were found to be required for efficient splicing. Mutations that delete this region or create polypurine insertions at position -2 had no significant effects on the efficiency of SV40 early pre-mRNA splicing in vivo or in vitro. Interestingly, however, the pyrimidine content of this region had substantial effects on the alternative splicing pattern of this pre-mRNA in vivo. Mutations that increased the number of pyrimidine residues resulted in more efficient utilization of the large T antigen mRNA 5' splice site relative to the small t 5' splice site, while mutations that increased the purine content enhanced small t mRNA splicing. A possible molecular mechanism for these findings, as well as a model that proposes a role for the polypyrimidine stretch in alternative splicing, are discussed.
我们研究了SV40早期区域3'剪接位点之前的核苷酸序列在mRNA前体剪接中的作用。有点令人惊讶的是,无论是高度保守的-3位置的嘧啶,还是相对于3'剪接位点从-5延伸至-15的多嘧啶序列,对于高效剪接而言都不是必需的。删除该区域或在-2位置产生多嘌呤插入的突变,对体内或体外SV40早期mRNA前体的剪接效率均无显著影响。然而,有趣的是,该区域的嘧啶含量对体内这种mRNA前体的可变剪接模式有实质性影响。增加嘧啶残基数量的突变导致相对于小t抗原mRNA 5'剪接位点,大T抗原mRNA 5'剪接位点的利用效率更高,而增加嘌呤含量的突变则增强了小t抗原mRNA的剪接。本文讨论了这些发现可能的分子机制,以及一个提出多嘧啶序列在可变剪接中作用的模型。