Woodbury N W, Dobres M, Thompson W F
Carnegie Institution of Washington, Stanford, CA 94305.
Curr Genet. 1989 Dec;16(5-6):433-45. doi: 10.1007/BF00340723.
We have used a novel approach to produce a comprehensive transcription initiation map of the pea chloroplast genome. Sites were mapped by measuring the ability of DNA probes to protect 5' ends of transcripts that have been capped in vitro. Using this approach, at least 33 probes appear to contain one or more transcription start sites. A more precise location of some of these sites was obtained by hybrid selecting certain of these RNAs and determining their size both before and after RNase treatment. We have found at least one initiation site in front of every chloroplast gene cluster for which appropriate clones were available. In addition, we have found initiation sites within gene clusters previously shown to be co-transcribed. In one such case, we were able to locate a transcription start site for psbC within the coding sequence of psbD.
我们采用了一种全新的方法来绘制豌豆叶绿体基因组的全面转录起始图谱。通过测量DNA探针保护体外加帽转录本5'端的能力来定位位点。使用这种方法,至少33个探针似乎包含一个或多个转录起始位点。通过杂交选择其中某些RNA并在核糖核酸酶处理前后确定其大小,获得了其中一些位点更精确的定位。对于每个有合适克隆的叶绿体基因簇,我们都发现了至少一个起始位点。此外,我们在先前显示为共转录的基因簇内也发现了起始位点。在其中一个这样的案例中,我们能够在psbD的编码序列内定位psbC的转录起始位点。