Biswas T K, Getz G S
Proc Natl Acad Sci U S A. 1986 Jan;83(2):270-4. doi: 10.1073/pnas.83.2.270.
The conserved nonanucleotide sequence functions as a promoter in the yeast (Saccharomyces cerevisiae) mitochondrial genome. A mitochondrial gene, Oli 1, which codes for ATPase subunit 9, has two identical nonanucleotide promoter sequences separated by 78 nucleotides, but they initiate transcription with very different efficiencies in vivo and in vitro. Deletion analysis has revealed that the nucleotide at position +2 of the weak downstream promoter accounts for its poor in vitro transcriptional activity. This finding was confirmed with site-specific mutations at +2 and +3 positions of a consensus synthetic promoter. The nonanucleotide mitochondrial promoter with a pyrimidine at position +2 acts as a weak promoter, whereas the same sequence with a purine at the +2 position functions as a strong promoter. The nucleotide at the +3 position further contributes to the relative promoter strength. These results suggest not only that the conserved nine-nucleotide sequence is required for the correct transcriptional initiation but also that other neighboring nucleotides influence the efficiency of promoter function.
保守的九核苷酸序列在酵母(酿酒酵母)线粒体基因组中作为启动子发挥作用。一个编码ATP酶亚基9的线粒体基因Oli 1,有两个相同的九核苷酸启动子序列,中间相隔78个核苷酸,但它们在体内和体外启动转录的效率非常不同。缺失分析表明,弱下游启动子+2位的核苷酸导致其体外转录活性较差。这一发现通过对共有合成启动子+2和+3位的位点特异性突变得到证实。+2位为嘧啶的九核苷酸线粒体启动子是弱启动子,而+2位为嘌呤的相同序列则作为强启动子发挥作用。+3位的核苷酸进一步影响启动子的相对强度。这些结果不仅表明保守的九核苷酸序列是正确转录起始所必需的,而且还表明其他相邻核苷酸会影响启动子功能的效率。