Stumpf G, Domdey H
Institut für Biochemie, Genzentrum, der Ludwig-Maximilians-Universität München Feodor-Lynen-Str. 25, D-81377 München, Germany.
Science. 1996 Nov 29;274(5292):1517-20. doi: 10.1126/science.274.5292.1517.
3'-End formation of pre-mRNA in yeast and mammals follows a similar but distinct pathway. In Saccharomyces cerevisiae, the cleavage reaction can be reconstituted by two activities called cleavage factor I and II (CFI and CFII). A CFII component, designated CFT1 (cleavage factor two) was identified by its sequence similarity to the AAUAAA-binding subunit of the mammalian cleavage and polyadenylation specificity factor (CPSF), even though the AAUAAA signal sequence appears to play no role in yeast pre-mRNA 3' processing. Depletion of a yeast whole-cell extract with antibodies to CFT1 protein abolished cleavage and polyadenylation of pre-mRNAs. Addition of CFII restored cleavage activity, but not polyadenylation. Polyadenylation required the further addition of poly(A) polymerase and polyadenylation factor I, suggesting a close but not necessarily direct association of these two factors with the CFT1 protein.
酵母和哺乳动物中前体mRNA的3'末端形成遵循相似但不同的途径。在酿酒酵母中,切割反应可由称为切割因子I和II(CFI和CFII)的两种活性重建。一种CFII组分,命名为CFT1(切割因子二),通过其与哺乳动物切割和聚腺苷酸化特异性因子(CPSF)的AAUAAA结合亚基的序列相似性而被鉴定,尽管AAUAAA信号序列似乎在酵母前体mRNA 3'加工中不起作用。用针对CFT1蛋白的抗体耗尽酵母全细胞提取物消除了前体mRNA的切割和聚腺苷酸化。添加CFII恢复了切割活性,但未恢复聚腺苷酸化。聚腺苷酸化需要进一步添加聚(A)聚合酶和聚腺苷酸化因子I,这表明这两个因子与CFT1蛋白有密切但不一定直接的关联。