Lilly J W, Havey M J, Jackson S A, Jiang J
Department of Horticulture, University of Wisconsin, Madison, Wisconsin 53706, USA.
Plant Cell. 2001 Feb;13(2):245-54. doi: 10.1105/tpc.13.2.245.
A DNA fiber-based fluorescence in situ hybridization (fiber-FISH) technique was developed to analyze the structure and organization of a large number of intact chloroplast DNA (cpDNA) molecules from Arabidopsis, tobacco, and pea. Using this cytogenomic approach, we determined that 25 to 45% of the cpDNA within developing leaf tissue consists of circular molecules. Both linear and circular DNA fibers with one to four copies of the chloroplast genome were present, with monomers being the predominant structure. Arabidopsis and tobacco chloroplasts contained previously unidentified multimers (>900 kb) consisting of six to 10 genome equivalents. We further discovered rearranged cpDNA molecules of incomplete genome equivalents, confirmed by both differential hybridizations and size estimations. The unique cpDNA organization and novel structures revealed in this study demonstrate that higher plant cpDNA is more structurally plastic than previous sequence and electrophoretic analyses have suggested. Additionally, we demonstrate how the fiber-FISH-based cytogenomic approach allows for powerful analysis of very rare events that cannot be detected by traditional techniques such as DNA gel blot hybridization or polymerase chain reaction.
一种基于DNA纤维的荧光原位杂交(纤维-FISH)技术被开发出来,用于分析来自拟南芥、烟草和豌豆的大量完整叶绿体DNA(cpDNA)分子的结构和组织。使用这种细胞基因组学方法,我们确定发育中的叶片组织内25%至45%的cpDNA由环状分子组成。存在具有一至四个叶绿体基因组拷贝的线性和环状DNA纤维,其中单体是主要结构。拟南芥和烟草叶绿体包含由六至十个基因组当量组成的先前未鉴定的多聚体(>900 kb)。我们进一步发现了基因组当量不完整的重排cpDNA分子,这通过差异杂交和大小估计得到证实。本研究中揭示的独特cpDNA组织和新结构表明,高等植物cpDNA在结构上比以前的序列和电泳分析所表明的更具可塑性。此外,我们展示了基于纤维-FISH的细胞基因组学方法如何能够对非常罕见的事件进行有力分析,而这些事件是传统技术如DNA凝胶印迹杂交或聚合酶链反应无法检测到的。