Institute of Agronomy and Plant Breeding I, Justus-Liebig-University, Ludwigstr. 23, D-35390, Giessen, Germany.
Theor Appl Genet. 1994 Oct;89(2-3):379-85. doi: 10.1007/BF00225170.
DNA from different male sterility-inducing sunflower cytoplasms was investigated in order to determine whether the cytoplasmic male sterility-inducing insertion of the PET1 mitochondrial DNA (mtDNA) is present in other cytoplasms. In one of these cytoplasms (MAX1) the mtDNA shows 93% sequence homology to the orfH522 of the PET1 mtDNA, which is probably responsible for cytoplasmic male sterility (cms) in the latter cytoplasm. In contrast to the situation in the PET1 mitochondrial genome, no transcription of the orfH522-related sequence could be detected in lines with the MAX1 cytoplasm. The organization of the MAX1 mtDNA and the mtDNA of a fertile line is shown to be widely different. In the study described here, homology to the mtDNA insertion was also detected in a fertile Helianthus maximiliani population, whereas DNA of four other H. maximiliani populations showed no hybridization signals.
为了确定是否存在其他细胞质雄性不育的 PET1 线粒体 DNA(mtDNA)插入,对来自不同雄性不育诱导向日葵细胞质的 DNA 进行了研究。在其中一种细胞质(MAX1)中,mtDNA 与 PET1 mtDNA 的 orfH522 有 93%的序列同源性,后者可能是后者细胞质雄性不育(cms)的原因。与 PET1 线粒体基因组的情况相反,在具有 MAX1 细胞质的系中,无法检测到 orfH522 相关序列的转录。MAX1 mtDNA 和可育系 mtDNA 的组织显示出广泛的不同。在本文所述的研究中,在一个可育的 Helianthus maximiliani 群体中也检测到了 mtDNA 插入的同源性,而其他四个 H. maximiliani 群体的 DNA 则没有杂交信号。