Guo Z, Sherman F
Department of Biochemistry, University of Rochester School of Medicine and Dentistry, New York 14642, USA.
Mol Cell Biol. 1995 Nov;15(11):5983-90. doi: 10.1128/MCB.15.11.5983.
It was previously shown that three distinct but interdependent elements are required for 3' end formation of mRNA in the yeast Saccharomyces cerevisiae: (i) the efficiency element TATATA and related sequences, which function by enhancing the efficiency of positioning elements; (ii) positioning elements, such as TTAAGAAC and AAGAA, which position the poly(A) site; and (iii) the actual site of polyadenylation. In this study, we have shown that several A-rich sequences, including the vertebrate poly(A) signal AATAAA, are also positioning elements. Saturated mutagenesis revealed that optimum sequences of the positioning element were AATAAA and AAAAAA and that this element can tolerate various extents of replacements. However, the GATAAA sequence was completely ineffective. The major cleavage sites determined in vitro corresponded to the major poly(A) sites observed in vivo. Our findings support the assumption that some components of the basic polyadenylation machinery could have been conserved among yeasts, plants, and mammals, although 3' end formation in yeasts is clearly distinct from that of higher eukaryotes.
先前的研究表明,酿酒酵母中mRNA 3'端形成需要三个不同但相互依存的元件:(i)效率元件TATATA及相关序列,其通过提高定位元件的效率发挥作用;(ii)定位元件,如TTAAGAAC和AAGAA,其定位聚腺苷酸化位点;(iii)实际的聚腺苷酸化位点。在本研究中,我们发现包括脊椎动物聚(A)信号AATAAA在内的几个富含A的序列也是定位元件。饱和诱变显示,定位元件的最佳序列是AATAAA和AAAAAA,并且该元件能够耐受不同程度的替换。然而,GATAAA序列完全无效。体外确定的主要切割位点与体内观察到的主要聚(A)位点相对应。我们的研究结果支持以下假设:尽管酵母中的3'端形成明显不同于高等真核生物,但基本聚腺苷酸化机制的某些成分可能在酵母、植物和哺乳动物中保守。