Sutton A, Broach J R
Mol Cell Biol. 1985 Oct;5(10):2770-80. doi: 10.1128/mcb.5.10.2770-2780.1985.
By S1 nuclease protection experiments and primer extension analysis, we determined precisely the cap and polyadenylation sites of transcripts from the four genes of the yeast 2 micron circle plasmid, as well as those of other plasmid transcripts of unknown function. In addition, we used deletion analysis to identify sequences necessary for polyadenylation in plasmid transcripts. Our results indicate that plasmid genes constitute independent transcription units and that plasmid mRNAs are not derived by extensive processing of precursor transcripts. In addition, we found that the D coding region of 2 micron circle is precisely encompassed by a polyadenylated transcript, suggesting that this coding region constitutes a functional plasmid gene. Our identification of the position of plasmid polyadenylation sites and of sequences necessary for polyadenylation provides support for a tripartite signal for polyadenylation as proposed by Zaret and Sherman (K.S. Zaret and F. Sherman, Cell 28:563-573, 1982). Finally, these data highlight salient features of the transcriptional regulatory circuitry that underlies the control of plasmid maintenance in the cell.
通过S1核酸酶保护实验和引物延伸分析,我们精确确定了酵母2μm环状质粒四个基因转录本的帽位点和聚腺苷酸化位点,以及其他功能未知的质粒转录本的相应位点。此外,我们利用缺失分析来鉴定质粒转录本中聚腺苷酸化所需的序列。我们的结果表明,质粒基因构成独立的转录单元,并且质粒mRNA并非通过前体转录本的广泛加工产生。此外,我们发现2μm环状质粒的D编码区恰好被一个聚腺苷酸化转录本所覆盖,这表明该编码区构成一个功能性质粒基因。我们对质粒聚腺苷酸化位点位置以及聚腺苷酸化所需序列的鉴定,为Zaret和Sherman(K.S. Zaret和F. Sherman,《细胞》28:563 - 573,1982)提出的聚腺苷酸化三方信号提供了支持。最后,这些数据突出了细胞中质粒维持控制所基于的转录调控回路的显著特征。