首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >THREE SINGLE-STRAND ORIGINS LOCATED ON BOTH STRANDS OF THE STREPTOMYCES ROLLING CIRCLE PLASMID PSN22
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THREE SINGLE-STRAND ORIGINS LOCATED ON BOTH STRANDS OF THE STREPTOMYCES ROLLING CIRCLE PLASMID PSN22

机译:链霉菌圆形质粒PSN22的两个链上都放置了三个单链原点

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pSN22 is an 11-kbp, high-copy-number Streptomyces plasmid which replicates via a single-stranded intermediate by the rolling circle replication (RCR) mechanism. We identified an unidirectional single-strand origin (SSO) of pSN22, ssol, where the initiation of second-strand synthesis takes place, located between the spdA and traR genes in a noncoding region which is functional in its natural orientation. The nucleotide sequence of ssol is similar over 170 bp to the SSOs of the Streptomyces plasmids PIJ101 and pJV1. A previous report described that a 548-bp BglII-SmaI fragment has an SSO activity (ori2; Kataoka el al., Mel. Gen. Genet. 242, 130-136, 1994). To our surprise, we discovered that on pSN22, the SSO in the BglII-SmaI fragment is in the wrong, inactive, orientation and thus cannot be involved in the conversion of the single-stranded pSN22 replication intermediate to the double-stranded form of the plasmid. We revealed that this BglII-SmaI fragment contains two SSO fragments. Secondary structure analysis of these two SSOs showed similarity to the consensus TAGCGT which is conserved in SSOs of RCR plasmids from Staphylococcus and the other several Gram-positive bacteria. Deletion of these hexanucleotide sequences caused loss of SSO activities. Our result shows that two types of SSOs, Streptomyces type and Staphylococcus-like type, can function in Streptomyces lividans. (C) 1997 Academic Press. [References: 31]
机译:pSN22是一种11 kbp,高拷贝数的链霉菌质粒,通过滚环复制(RCR)机制通过单链中间体进行复制。我们确定了pSN22 ssol的单向单链起源(SSO),其中第二链合成的起始发生在非编码区域的spdA和traR基因之间,该区域在其自然方向上具有功能。固溶体的核苷酸序列在170bp以上与链霉菌质粒PIJ101和pJV1的SSO相似。先前的报道描述了548bp的BglII-SmaI片段具有SSO活性(ori2; Kataoka等人,Mel.Gen.Genet.242,130-136,1994)。令我们惊讶的是,我们发现在pSN22上,BglII-SmaI片段中的SSO处于错误,无活性的方向,因此不能参与将单链pSN22复制中间体转化为双链形式的SSN。质粒。我们发现该BglII-SmaI片段包含两个SSO片段。这两个SSO的二级结构分析显示与共有TAGCGT相似,TAGCGT在葡萄球菌和其他几种革兰氏阳性细菌的RCR质粒的SSO中保守。这些六核苷酸序列的缺失导致SSO活性的丧失。我们的结果表明,两种类型的SSO,即链霉菌型和葡萄球菌样型,都可以在青霉链霉菌中起作用。 (C)1997学术出版社。 [参考:31]

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