Jenny A, Minvielle-Sebastia L, Preker P J, Keller W
Department of Cell Biology, Biozentrum, University of Basel, CH-4056 Basel, Switzerland.
Science. 1996 Nov 29;274(5292):1514-7. doi: 10.1126/science.274.5292.1514.
The 3' ends of most eukaryotic messenger RNAs are generated by endonucleolytic cleavage and polyadenylation. In mammals, the cleavage and polyadenylation specificity factor (CPSF) plays a central role in both steps of the processing reaction. Here, the cloning of the 73-kilodalton subunit of CPSF is reported. Sequence analyses revealed that a yeast protein (Ysh1) was highly similar to the 73-kD polypeptide. Ysh1 constitutes a new subunit of polyadenylation factor I (PFI), which has a role in yeast pre-mRNA 3'-end formation. This finding was unexpected because in contrast to CPSF, PFI is only required for the polyadenylation reaction. These results contribute to the understanding of how 3'-end processing factors may have evolved.
大多数真核生物信使核糖核酸(mRNA)的3'末端是通过核酸内切酶切割和聚腺苷酸化产生的。在哺乳动物中,切割和聚腺苷酸化特异性因子(CPSF)在加工反应的这两个步骤中都起着核心作用。在此,报道了CPSF 73千道尔顿亚基的克隆。序列分析表明,一种酵母蛋白(Ysh1)与73-kD多肽高度相似。Ysh1构成聚腺苷酸化因子I(PFI)的一个新亚基,PFI在酵母前体mRNA 3'末端形成中起作用。这一发现出乎意料,因为与CPSF不同,PFI仅在聚腺苷酸化反应中是必需的。这些结果有助于理解3'末端加工因子可能是如何进化的。