Carrillo N, Bogorad L
Biological Laboratories, Harvard University, Cambridge, MA 02138.
Nucleic Acids Res. 1988 Jun 24;16(12):5603-20. doi: 10.1093/nar/16.12.5603.
An enzyme system prepared from maize chloroplasts catalyzes the synthesis of DNA from maize chloroplast DNA sequences cloned in bacterial plasmids. Cloned maize chloroplast DNA fragments Bam HI 17' (2470 bp) and Eco RI x (1368 bp) have been shown to be preferred templates for in vitro DNA synthesis catalyzed by pea chloroplast DNA polymerase preparations [Gold et al. (1987) Proc. Natl. Acad. Sci. USA 84, 194-198]. Analysis of replicative intermediates indicates that although the template activity of the recombinant plasmid pZmcBam 17' is substantially greater than that of the pZmcEco x, replication in both cases originates from within a 455 bp region which overlaps the two plasmids. The remaining approximately 1500 basepair portion of maize chloroplast BamHI fragment 17' is not more active because it contains additional origins for replication. The overlapping region shows sequence homology with a portion of the Chlamydomonas reinhardtii chloroplast chromosome that contains a replication origin. Replication is shown to proceed bidirectionally within the 455 bp origin region. Recombinant plasmid pZmc 427, which is also active in the in vitro DNA synthesis assay, promoted localized replication initiation within a 1 kbp Bg1II-Eco RI fragment of the chloroplast DNA insert, a region that includes the 3' terminal part of the psbA gene.
从玉米叶绿体中制备的一种酶系统可催化由克隆在细菌质粒中的玉米叶绿体DNA序列合成DNA。已证明克隆的玉米叶绿体DNA片段Bam HI 17'(2470 bp)和Eco RI x(1368 bp)是豌豆叶绿体DNA聚合酶制剂催化的体外DNA合成的优选模板[戈尔德等人(1987年)《美国国家科学院院刊》84,194 - 198]。对复制中间体的分析表明,尽管重组质粒pZmcBam 17'的模板活性远高于pZmcEco x,但在这两种情况下复制均起始于一个与两个质粒重叠的455 bp区域内。玉米叶绿体BamHI片段17'其余约1500个碱基对部分活性不高,因为它包含额外的复制起点。重叠区域与莱茵衣藻叶绿体染色体中包含复制起点的一部分显示出序列同源性。已证明复制在455 bp起点区域内双向进行。在体外DNA合成测定中也有活性的重组质粒pZmc 427促进了叶绿体DNA插入片段的一个1 kbp Bg1II - Eco RI片段内的局部复制起始,该区域包括psbA基因的3'末端部分。