Vera A, Sugiura M
Center for Gene Research, Nagoya University, Japan.
EMBO J. 1994 May 1;13(9):2211-7. doi: 10.1002/j.1460-2075.1994.tb06498.x.
A small plastid-encoded RNA (spRNA, 218 nt) has been detected in tobacco. The corresponding locus (sprA) does not contain any open reading frame and is actively transcribed from its own promoter, as shown by ribonuclease protection assays using in vitro capped RNAs. Gel-shift and UV-crosslinking experiments showed the formation of a specific complex between spRNA and chloroplast polypeptides. The mobility of the complex was further shifted when a transcript bearing part of the 16S rRNA leader sequence was added to the incubation mixture. Glycerol gradient fractionation of a chloroplast lysate indicated a preferential sedimentation of spRNA at 15-20S and 70S. These observations, and the potential base-pairing with the leader sequence of pre-16S rRNA, suggest a role for spRNA in chloroplast ribosome biogenesis, i.e. 16S rRNA maturation. By sequencing of tomato plastid DNA and heterologous northern hybridizations, the presence of sprA homologs and their expression in a number of dicot plants have also been shown.
在烟草中检测到一种小的质体编码RNA(spRNA,218个核苷酸)。相应的基因座(sprA)不包含任何开放阅读框,并且如使用体外加帽RNA的核糖核酸酶保护试验所示,它从自身启动子进行活跃转录。凝胶迁移和紫外线交联实验表明spRNA与叶绿体多肽之间形成了特异性复合物。当将带有16S rRNA前导序列部分的转录本添加到孵育混合物中时,复合物的迁移率进一步发生改变。叶绿体裂解物的甘油梯度分级分离表明spRNA优先沉降在15 - 20S和70S处。这些观察结果以及与前体16S rRNA前导序列的潜在碱基配对,表明spRNA在叶绿体核糖体生物发生中起作用,即16S rRNA成熟。通过对番茄质体DNA进行测序和异源Northern杂交,还证明了sprA同源物在许多双子叶植物中的存在及其表达。