Gold B, Carrillo N, Tewari K K, Bogorad L
Proc Natl Acad Sci U S A. 1987 Jan;84(1):194-8. doi: 10.1073/pnas.84.1.194.
Maize chloroplast DNA sequences representing 94% of the chromosome have been surveyed for their activity as autonomously replicating sequences in yeast and as templates for DNA synthesis in vitro by a partially purified chloroplast DNA polymerase. A maize chloroplast DNA region extending over about 9 kilobase pairs is especially active as a template for the DNA synthesis reaction. Fragments from within this region are much more active than DNA from elsewhere in the chromosome and 50- to 100-fold more active than DNA of the cloning vector pBR322. The smallest of the strongly active subfragments that we have studied, the 1368-base-pair EcoRI fragment x, has been sequenced and found to contain the coding region of chloroplast ribosomal protein L16. EcoRI fragment x shows sequence homology with a portion of the Chlamydomonas reinhardtii chloroplast chromosome that forms a displacement loop [Wang, X.-M., Chang, C.H., Waddell, J. & Wu, M. (1984) Nucleic Acids Res. 12, 3857-3872]. Maize chloroplast DNA fragments that permit autonomous replication of DNA in yeast are not active as templates for DNA synthesis in the in vitro assay. The template active region we have identified may represent one of the origins of replication of maize chloroplast DNA.
已对代表玉米染色体94%的叶绿体DNA序列进行了研究,检测其作为酵母中自主复制序列的活性,以及作为部分纯化的叶绿体DNA聚合酶体外DNA合成模板的活性。一个延伸约9千碱基对的玉米叶绿体DNA区域作为DNA合成反应的模板特别活跃。该区域内的片段比染色体其他部位的DNA活性高得多,比克隆载体pBR322的DNA活性高50至100倍。我们研究的活性最强的亚片段中最小的一个,即1368碱基对的EcoRI片段x,已进行测序,发现其包含叶绿体核糖体蛋白L16的编码区。EcoRI片段x与莱茵衣藻叶绿体染色体中形成置换环的一部分显示出序列同源性[王,X.-M.,张,C.H.,沃德尔,J. & 吴,M.(1984年)《核酸研究》12,3857 - 3872]。在酵母中允许DNA自主复制的玉米叶绿体DNA片段在体外测定中作为DNA合成模板没有活性。我们鉴定出的模板活性区域可能代表玉米叶绿体DNA的复制起点之一。