Russell D, Bogorad L
Nucleic Acids Res. 1987 Feb 25;15(4):1853-67. doi: 10.1093/nar/15.4.1853.
Maize seedlings contain several RNA species complementary to the rpS4 coding strand of the maize chloroplast ribosomal protein gene rpS4. All of these have the same 5' end about 182 bp upstream of the translation start codon for the protein S4. Northern and S1 nuclease analyses of RNA isolated from seedlings at different stages of greening show that the size of the pool of rpS4 transcripts does not change significantly upon illumination of dark-grown seedlings. The rpS4 gene has also been analyzed by in vitro transcription using maize chloroplast RNA polymerase preparations. The site of initiation in vitro has been mapped by S1 nuclease analysis to the same location as the 5' terminus of in vivo transcripts. A sequence resembling other plastid promoters occurs just upstream of this initiation site. The sensitivity of in vitro transcription to DNA template superhelicity has been assessed for the rpS4 gene promoter; its negative superhelicity-transcription rate profile resembles that of rbcL.
玉米幼苗含有几种与玉米叶绿体核糖体蛋白基因rpS4的rpS4编码链互补的RNA种类。所有这些RNA的5'端都在蛋白质S4翻译起始密码子上游约182 bp处。对从不同绿化阶段的幼苗中分离的RNA进行的Northern和S1核酸酶分析表明,黑暗生长的幼苗光照后,rpS4转录本库的大小没有显著变化。还使用玉米叶绿体RNA聚合酶制剂通过体外转录对rpS4基因进行了分析。通过S1核酸酶分析将体外起始位点定位到与体内转录本5'末端相同的位置。在该起始位点上游刚好出现一个类似于其他质体启动子的序列。已评估了rpS4基因启动子对DNA模板超螺旋的体外转录敏感性;其负超螺旋-转录速率曲线类似于rbcL的曲线。