Vegetable Crops Department, University of Florida, 32611, Gainesville, FL, U.S.A..
Plant Mol Biol. 1986 Jan;6(1):53-64. doi: 10.1007/BF00021306.
The linear N1 and N2 plasmid-like DNAs were recovered from mitochondria of the IS1112C line of cytoplasmic male-sterile (CMS) Sorghum bicolor (S. bicolor). Molecular clones containing internal sequences of these plasmids were constructed. These clones were used to probe Southern blots of mitochondrial genomes from six CMS and five male-fertile (MF) lines of S. bicolor, as well as Southern blots of IS1112C chloroplast, IS1112C nuclear and kafir nuclear genomes. We found no evidence for integrated copies of N1 or N2 in any of the mitochondrial, chloroplast or nuclear genomes probed in this study. Our clones did detect an N1-homologous transcript of 3.1 kb and N2-homologous transcripts of 3.9 and 1.4 kb in IS1112C mitochondrial RNA prepared from lines with and without nuclear, fertility-restoring genes.N1 and N2 DNAs were degraded by exonuclease III but were resistant to lambda exonuclease, presumably due to the presence of 5' terminal proteins. We detected multimeric forms of N1 and N2 in Southern blots of unrestricted, IS1112C mitochondrial DNA (mtDNA). These forms apparently also had associated protein molecules.
从细胞质雄性不育(CMS)高粱 IS1112C 系的线粒体中回收了线性 N1 和 N2 质粒样 DNA。构建了含有这些质粒内部序列的分子克隆。这些克隆被用于探测来自六个 CMS 和五个雄性可育(MF)高粱系的线粒体基因组的 Southern 印迹,以及探测 IS1112C 叶绿体、IS1112C 核和卡菲尔核基因组的 Southern 印迹。我们在本研究探测的任何线粒体、叶绿体或核基因组中都没有发现 N1 或 N2 整合拷贝的证据。我们的克隆确实在有核、育性恢复基因的 IS1112C 线粒体 RNA 中检测到 3.1 kb 的 N1 同源转录物和 3.9 kb 和 1.4 kb 的 N2 同源转录物。N1 和 N2 DNA 被外切核酸酶 III 降解,但对 λ外切核酸酶有抗性,可能是由于存在 5'末端蛋白。我们在不受限制的 IS1112C 线粒体 DNA(mtDNA)的 Southern 印迹中检测到 N1 和 N2 的多聚体形式。这些形式显然也有相关的蛋白质分子。