Hiratsu K, Mochizuki S, Kinashi H
Department of Fermentation Technology, Hiroshima University, Higashi-Hiroshima, Japan.
Mol Gen Genet. 2000 Jul;263(6):1015-21. doi: 10.1007/pl00008689.
The replication origin and both terminal segments were cloned from the large linear plasmid pSLA2-L in Streptomyces rochei 7434AN4. The basic replicon consists of a 1.9-kb DNA fragment, which contains the genetic information required for autonomous replication in circular form. Sequence analysis revealed two ORFs, RepL1 and RepL2, with no similarity to any of the replication initiator proteins in the database. Deletion and mutational analysis showed that RepL1 is essential for replication and RepL2 has a subsidiary function. The origin of replication may be located 800 bp upstream of repL1. Sequencing of the left and right terminal segments revealed the presence of 12 palindromes. The sequence of the first 90 bp, including palindromes I-IV, shows great similarity to that of other Streptomyces linear chromosomes and plasmids. These results suggest that the internal replication origins of the linear replicons vary widely, in contrast to the high degree of conservation of their telomeres.
复制起点和两个末端片段是从罗氏链霉菌7434AN4中的大型线性质粒pSLA2-L克隆而来的。基本复制子由一个1.9 kb的DNA片段组成,该片段包含以环状形式自主复制所需的遗传信息。序列分析揭示了两个开放阅读框(ORF),RepL1和RepL2,它们与数据库中的任何复制起始蛋白均无相似性。缺失和突变分析表明,RepL1对复制至关重要,而RepL2具有辅助功能。复制起点可能位于repL1上游800 bp处。左右末端片段的测序显示存在12个回文序列。包括回文序列I-IV在内的前90 bp的序列与其他链霉菌线性染色体和质粒的序列具有高度相似性。这些结果表明,与端粒的高度保守性相反,线性复制子的内部复制起点差异很大。