Vera A, Sugiura M
Center for Gene Research, Nagoya University, Japan.
Curr Genet. 1995 Feb;27(3):280-4. doi: 10.1007/BF00326161.
Identification of transcription initiation sites in the promoter region of the tobacco chloroplast rRNA operon has been carried out by ribonuclease protection of in vitro capped RNAs and primer extension experiments. A promoter with typical chloroplast -10 and -35 motifs (P1) drives initiation of transcription from position -116 relative to the mature 16s rRNA sequence. In addition, we have found that a second primary transcript starts at position -64. This proximal promoter (P2) lacks any elements similar to those reported so far in chloroplast promoter regions, and hence P2 represents a novel-type promoter. Both transcripts are present in chloroplasts from green leaves and in non-photosynthetic proplastids from heterotrophically cultured cells (BY2), but their relative amounts appear to differ. The steady state level of the P2 transcript, with respect to P1, is higher in BY2 proplastids than in leaf chloroplasts.
通过对体外加帽RNA进行核糖核酸酶保护和引物延伸实验,已确定了烟草叶绿体rRNA操纵子启动子区域的转录起始位点。一个具有典型叶绿体-10和-35基序的启动子(P1)驱动相对于成熟16S rRNA序列从-116位开始转录。此外,我们发现第二个初级转录本从-64位开始。这个近端启动子(P2)缺乏迄今在叶绿体启动子区域报道的任何类似元件,因此P2代表一种新型启动子。两种转录本都存在于绿叶的叶绿体和异养培养细胞(BY2)的非光合前质体中,但它们的相对含量似乎有所不同。相对于P1,P2转录本的稳态水平在BY2前质体中比在叶叶绿体中更高。