Department of Cell Biology, Roche Institute of Molecular Biology, Roche Research Center, 07110, Nutley, NJ, USA.
Plant Cell Rep. 1985 Apr;4(2):41-5. doi: 10.1007/BF00269202.
A simple method using molecular hybridization was devised to quantitatively measure chloroplast DNA synthesis in vivo. Total cellular DNA isolated from Nicotiana tabacum suspension cells, labeled with (3)H-thymidine, was hybridized to nitrocellulose membrane-bound cloned chloroplast DNA (ct DNA) fragments. Colorless, dark grown N. tabacum cells were found to contain approximately 3300-4800 chloroplast genome copies per cell, whereas light grown, green cells contain about 9500-12000 chloroplast genomes per cell. This difference in ct DNA levels suggests that the chloroplast genome is somewhat amplified during growth of the cells in the light. The hybridization technique was also used to measure the efficiency of hybridization between cloned spinach ct DNA and tobacco ct DNA. The two DNAs were found to cross-hybridize with an efficiency of 69-75%.
设计了一种使用分子杂交的简单方法来定量测量体内叶绿体 DNA 的合成。从烟草悬浮细胞中分离出用[3H]胸腺嘧啶标记的总细胞 DNA,与硝酸纤维素膜结合的克隆叶绿体 DNA(ctDNA)片段进行杂交。无色、暗培养的烟草细胞每细胞含有约 3300-4800 个叶绿体基因组拷贝,而光照、绿色的细胞每细胞含有约 9500-12000 个叶绿体基因组。ctDNA 水平的这种差异表明,叶绿体基因组在细胞的光照生长过程中略有扩增。该杂交技术还用于测量克隆菠菜 ctDNA 和烟草 ctDNA 之间杂交效率。发现这两种 DNA 的杂交效率为 69-75%。