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双向酵母TRP4 mRNA 3'端形成信号的序列要求。

Sequence requirements of the bidirectional yeast TRP4 mRNA 3'-end formation signal.

作者信息

Egli C M, Düvel K, Trabesinger-Rüf N, Irniger S, Braus G H

机构信息

Institute of Microbiology, Georg-August University, Grisebachstrasse 8, D-37077 Göttingen, Germany.

出版信息

Nucleic Acids Res. 1997 Jan 15;25(2):417-22. doi: 10.1093/nar/25.2.417.

Abstract

The yeast TRP4 3'-end formation signal functions in both orientations in an in vivo test system. We show here that the TRP4 3'-end formation element consists of two functionally different sequence regions. One region of approximately 70 nucleotides is located in the untranslated region between the translational stop codon and the major poly(A) site. The major poly(A) site is not part of this region and can be deleted without a decrease in TRP4 3'-end formation. 5'and 3'deletions and point mutations within this region affected 3'-end formation similarly in both orientations. In the center of this region the motif TAGT is located on the antisense strand. Point mutations within this motif resulted in a drastic reduce of 3'-end formation activity in both orientations. A second region consists of the 3'-end of the TRP4 open reading frame and is required for 3'-end formation in forward orientation. A single point mutation in a TAGT motif of the TRP4 open reading frame abolished TRP4 mRNA 3'-end formation in forward orientation and had no effect on the reverse orientation.

摘要

酵母TRP4 3'端形成信号在体内测试系统中以两种方向发挥作用。我们在此表明,TRP4 3'端形成元件由两个功能不同的序列区域组成。一个约70个核苷酸的区域位于翻译终止密码子和主要聚腺苷酸化位点之间的非翻译区域。主要聚腺苷酸化位点不是该区域的一部分,删除后TRP4 3'端形成不会减少。该区域内的5'和3'缺失及点突变在两个方向上对3'端形成的影响相似。在该区域的中心,基序TAGT位于反义链上。该基序内的点突变导致两个方向上3'端形成活性急剧降低。第二个区域由TRP4开放阅读框的3'端组成,是正向3'端形成所必需的。TRP4开放阅读框的TAGT基序中的单个点突变消除了正向TRP4 mRNA 3'端的形成,而对反向没有影响。

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