Berquist Brian R, DasSarma Shiladitya
Molecular and Cell Biology Program, University of Maryland, Baltimore, and Center of Marine Biotechnology, University of Maryland Biotechnology Institute, Baltimore, Maryland 21202, USA.
J Bacteriol. 2003 Oct;185(20):5959-66. doi: 10.1128/JB.185.20.5959-5966.2003.
We report on the identification and first cloning of an autonomously replicating sequence element from the chromosome of an archaeon, the extreme halophile Halobacterium strain NRC-1. The putative replication origin was identified by association with the orc7 gene and replication ability in the host strain, demonstrated by cloning into a nonreplicating plasmid. Deletion analysis showed that sequences located up to 750 bp upstream of the orc7 gene translational start, plus the orc7 gene and 50 bp downstream, are sufficient to endow the plasmid with replication ability, as judged by expression of a plasmid-encoded mevinolin resistance selectable marker and plasmid recovery after transformation. Sequences located proximal to the two other chromosomally carried haloarchaeal orc genes (orc6 and orc8) are not able to promote efficient autonomous replication. Located within the 750-bp region upstream of orc7 is a nearly perfect inverted repeat of 31 bp, which flanks an extremely AT-rich (44%) stretch of 189 bp. The replication ability of the plasmid was lost when one copy of the inverted repeat was deleted. Additionally, the inverted repeat structure near orc7 homologs in the genomic sequences of two other halophiles, Haloarcula marismortui and Haloferax volcanii, is highly conserved. Our results indicate that, in halophilic archaea, a chromosomal origin of replication is physically linked to orc7 homologs and that this element is sufficient to promote autonomous replication. We discuss the finding of a functional haloarchaeal origin in relation to the large number of orc1-cdc6 homologs identified in the genomes of all haloarchaea to date.
我们报告了从嗜盐古菌嗜盐栖热菌菌株NRC-1的染色体中鉴定并首次克隆出一个自主复制序列元件。通过与orc7基因的关联以及在宿主菌株中的复制能力鉴定出假定的复制起点,这通过克隆到非复制性质粒中得以证明。缺失分析表明,位于orc7基因翻译起始位点上游达750 bp的序列,加上orc7基因及其下游50 bp,足以赋予质粒复制能力,这通过质粒编码的美伐他汀抗性选择标记的表达以及转化后质粒的回收来判断。位于另外两个染色体携带的嗜盐古菌orc基因(orc6和orc8)附近的序列不能促进高效自主复制。在orc7上游的750 bp区域内有一个近乎完美的31 bp反向重复序列,其两侧是一段189 bp的富含AT(44%)的序列。当一个反向重复序列拷贝被删除时,质粒的复制能力丧失。此外,在另外两种嗜盐菌盐沼盐杆菌和嗜热栖热菌的基因组序列中,orc7同源物附近的反向重复结构高度保守。我们的结果表明,在嗜盐古菌中,染色体复制起点与orc7同源物在物理上相关联,并且该元件足以促进自主复制。我们讨论了与迄今为止在所有嗜盐古菌基因组中鉴定出的大量orc1-cdc6同源物相关的功能性嗜盐古菌复制起点的发现。