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酿酒酵母基因RHO1和MRP2的趋同与重叠转录单元中mRNA 3'端形成信号的功能分析

Functional analysis of mRNA 3' end formation signals in the convergent and overlapping transcription units of the S. cerevisiae genes RHO1 and MRP2.

作者信息

Peterson J A, Myers A M

机构信息

Department of Biochemistry and Biophysics, Iowa State University, Ames 50011.

出版信息

Nucleic Acids Res. 1993 Nov 25;21(23):5500-8. doi: 10.1093/nar/21.23.5500.

Abstract

The Saccharomyces cerevisiae genes RHO1 and MRP2 are convergently transcribed, with 281 base pairs separating their termination codons. Transcript mapping revealed at least 111 base pairs within the RHO1-MRP2 intercoding region are transcribed in both directions. Transplacement experiments showed distinct sequences of 70 nt for MRP2 and 179 nt for RHO1 were sufficient for normal mRNA 3' end formation. The MRP2 signal functioned in either orientation, although relatively inefficiently in the non-native orientation. This element contains a polyAT sequence essential for 3' end formation in both orientations. RHO1 or MRP2 3' end formation was not affected by overproduction or elimination of the complementary, natural antisense transcript. In contrast, insertion of a strong promoter that extended antisense transcripts beyond their normal 3' ends inactivated either MRP2 or RHO1. These data suggest that transcript termination in the compact yeast genome can be important to prevent inactivation of downstream genes as a result of antisense transcription.

摘要

酿酒酵母基因RHO1和MRP2是反向转录的,它们的终止密码子之间相隔281个碱基对。转录图谱显示,RHO1 - MRP2编码间隔区内至少111个碱基对是双向转录的。转位实验表明,MRP2的70个核苷酸和RHO1的179个核苷酸的不同序列足以实现正常的mRNA 3'端形成。MRP2信号在任一方向都起作用,尽管在非天然方向效率相对较低。该元件包含一个对两个方向的3'端形成都至关重要的聚腺苷酸序列。RHO1或MRP2的3'端形成不受互补的天然反义转录本过量产生或消除的影响。相反,插入一个强大的启动子使反义转录本延伸超过其正常的3'端会使MRP2或RHO1失活。这些数据表明,紧密的酵母基因组中的转录终止对于防止反义转录导致下游基因失活可能很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8193/310593/f031f74f3409/nar00072-0224-a.jpg

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