Pichersky E, Logsdon J M, McGrath J M, Stasys R A
Department of Biology, University of Michigan, Ann Arbor 48109.
Mol Gen Genet. 1991 Mar;225(3):453-8. doi: 10.1007/BF00261687.
We have undertaken a systematic search for plastid DNA sequences integrated in the tomato nuclear genome, using heterologous probes taken from intervals of a plastid DNA region spanning 58 kb. A total of two short integrates (202 and 141 nucleotides) were isolated and mapped to chromosomes 9 and 5, respectively. The nucleotide sequence of the integrates and that of the flanking regions were determined. The integration sites contain direct repeat elements similar in position (but not in length or sequence) to the direct repeats previously observed with another plastid integrate in the tomato nuclear genome. Based on these results, a model for the process of movement and integration of plastid sequences into the nuclear genome is discussed.
我们利用取自跨越58 kb的叶绿体DNA区域间隔的异源探针,对整合到番茄核基因组中的叶绿体DNA序列进行了系统搜索。总共分离出两个短整合片段(202和141个核苷酸),分别定位到9号和5号染色体上。测定了整合片段及其侧翼区域的核苷酸序列。整合位点包含与之前在番茄核基因组中观察到的另一个叶绿体整合片段中直接重复序列位置相似(但长度或序列不同)的直接重复元件。基于这些结果,讨论了叶绿体序列向核基因组移动和整合过程的模型。