Gruissem W, Elsner-Menzel C, Latshaw S, Narita J O, Schaffer M A, Zurawski G
Nucleic Acids Res. 1986 Oct 10;14(19):7541-56. doi: 10.1093/nar/14.19.7541.
We have identified a class of spinach plastid tRNA genes which do not require 5' upstream promoter elements for their expression in a chloroplast transcription system. The 5' DNA sequences flanking the trnR1 and trnS1 coding regions have little or no homology to previously characterized chloroplast promoter sequences. The deletion of the 5' DNA sequences from these genes to positions close to the start of the coding regions has little effect on their transcription in vitro. In addition, a synthetic DNA fragment homologous to the 5' region of trnS1 does not support the transcription of the promoter (-) trnM2 mutant 51 in a promoter/trnM2-51 fusion assay. In a dicistronic construct the wild type trnS1 gene does not support transcription of trnS1 transcription occurs immediately following the 3' end of the coding region. Both trnS1 and trnR1 compete with trnM2 for the same chloroplast RNA polymerase and/or common transcription factors.
我们已经鉴定出一类菠菜质体tRNA基因,它们在叶绿体转录系统中表达时不需要5'上游启动子元件。位于trnR1和trnS1编码区侧翼的5' DNA序列与先前鉴定的叶绿体启动子序列几乎没有同源性。从这些基因中删除5' DNA序列至接近编码区起始位置,对其体外转录影响很小。此外,在启动子/trnM2-51融合检测中,与trnS1 5'区域同源的合成DNA片段不能支持启动子(-)trnM2突变体51的转录。在双顺反子构建体中,野生型trnS1基因不能支持trnS1的转录,转录在编码区3'末端之后立即发生。trnS1和trnR1都与trnM2竞争相同的叶绿体RNA聚合酶和/或共同转录因子。