Cannon G C, Hedrick L A, Heinhorst S
Department of Chemistry and Biochemistry, University of Southern Mississippi, Hattiesburg 39406-5043, USA.
Plant Mol Biol. 1995 Dec;29(6):1267-77. doi: 10.1007/BF00020467.
In order to better understand the biochemical mechanisms of DNA metabolism in chloroplasts, repair of UV induced plastome damage in vivo was determined by exposure of soybean suspension cells to UV light and subsequent quantitation of the damage remaining in nuclear and chloroplast encoded genes with time by quantitative polymerase chain reaction (QPCR). The kinetics of damage repair in the nuclear rbcS gene suggest that photoreactivation and dark mechanisms are active, while for the plastome encoded psbA gene only a light-dependent repair process was detected which is considerably slower than would be expected for photolyase-mediated photoreactivation.
为了更好地理解叶绿体中DNA代谢的生化机制,通过将大豆悬浮细胞暴露于紫外线下,然后利用定量聚合酶链反应(QPCR)随时间对核编码基因和叶绿体编码基因中残留的损伤进行定量,来测定体内紫外线诱导的质体基因组损伤的修复情况。核rbcS基因损伤修复的动力学表明,光复活和暗修复机制均起作用,而对于质体基因组编码的psbA基因,仅检测到一个光依赖的修复过程,该过程比光解酶介导的光复活预期的要慢得多。