Centro de Investigaciones Biológicas, C.S.I.C., Madrid, Spain.
Plant Mol Biol. 1988 Sep;10(5):413-22. doi: 10.1007/BF00014947.
The replication origin (ori-r9) of the 9.0 kb rDNA repeats of pea (Pisum sativum, cv. Alaska) was cloned and found to reside in a 1.5 kb fragment of the non-transcribed spacer region located between the 25 S and 18 S genes. Labeled rDNA rich in replication forks, from cells positioned at the G1/S phase boundary, was used to map ori-r9 by hybridization procedures. Ori-r9 is in a 210-base fragment that is 1.6 kb from the 5' end of the 18 S gene and about 1.5 kb from the 3' end of the 25 S gene. The same procedures, using labeled synthetic ARS consensus sequence as a probe, showed than an ARS consensus sequence is located 3' to ori-r9 in a 710-base fragment. An ARS consensus sequence is, therefore, adjacent to ori-r9 but not coincidental with it.
豌豆(Pisum sativum,cv. Alaska)9.0 kb rDNA 重复序列的复制起点(ori-r9)被克隆,并发现其位于位于 25S 和 18S 基因之间的非转录间隔区 1.5kb 片段内。用富含复制叉的标记 rDNA 从处于 G1/S 期边界的细胞中进行杂交程序,以定位 ori-r9。ori-r9 位于 210 碱基片段中,距离 18S 基因 5'端 1.6kb,距离 25S 基因 3'端约 1.5kb。同样的程序,使用标记的合成 ARS 共有序列作为探针,表明一个 ARS 共有序列位于 ori-r9 的 3'端,在一个 710 碱基片段中。因此,ARS 共有序列紧邻 ori-r9,但不与其重合。