Faculty of Agronomic Sciences, Unit of Genetics and Plant Improvement, B-5800, Gembloux, Belgium.
Theor Appl Genet. 1990 Jun;79(6):807-12. doi: 10.1007/BF00224249.
Potato plastid DNA clones, representing onefourth of the potato plastome complexity and containing sequences of the 16SrRNA, rps16, atpA, atpE, psaA, psaB, trnK, trnV, and trnG genes, were used as hybridization probes on nuclear- and mitochondrial-enriched DNAs. Each probe hybridized to multiple nuclear restriction fragments distinct from the plastid cleavage products generated by the same endonucleases. The nuclear hybridizable fragments are highly methylated at their Hpall target sequences (C/CGG). In some instances, the transfer seemed to involve plastid regions of several kilobase pairs, as reflected by the co-integration in the nucleus of restriction sites that are distant in the plastome. Three clones hybridized additionally to distinct mitochondrial fragments. These results indicate that extensive DNA transfers did occur between plastids and other organelles in potato.
马铃薯质体 DNA 克隆,代表四分之一的马铃薯质体复杂性,包含 16SrRNA、rps16、atpA、atpE、psaA、psaB、trnK、trnV 和 trnG 基因的序列,被用作核和线粒体富集 DNA 的杂交探针。每个探针与多个不同于相同内切酶产生的质体切割产物的核限制片段杂交。核可杂交片段在其 Hpall 靶序列(C/CGG)处高度甲基化。在某些情况下,这种转移似乎涉及几个千碱基对的质体区域,这反映在核中整合了在质体中相距很远的限制位点。三个克隆还与不同的线粒体片段杂交。这些结果表明,在马铃薯中,质体与其他细胞器之间确实发生了广泛的 DNA 转移。