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三个单链起始位点位于链霉菌滚环质粒pSN22的两条链上。

Three single-strand origins located on both strands of the Streptomyces rolling circle plasmid pSN22.

作者信息

Suzuki I, Kataoka M, Seki T, Yoshida T

机构信息

Osaka University, 2-1 Yamada-oka, Suita, Osaka, 565, Japan.

出版信息

Plasmid. 1997;37(1):51-64. doi: 10.1006/plas.1996.1269.

Abstract

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, sso1, 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 sso1 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 et al., Mol. 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.

摘要

pSN22是一个11千碱基对的高拷贝数链霉菌质粒,它通过滚环复制(RCR)机制经单链中间体进行复制。我们鉴定出pSN22的一个单向单链起始位点(SSO),即sso1,第二链合成在此起始,它位于spdA和traR基因之间的一个非编码区,该区域在其天然方向上具有功能。sso1的核苷酸序列在170碱基对范围内与链霉菌质粒pIJ101和pJV1的SSO相似。之前的一份报告描述一个548碱基对的BglII - SmaI片段具有SSO活性(ori2;片冈等人,《分子与普通遗传学》242卷,130 - 136页,1994年)。令我们惊讶的是,我们发现对于pSN22,BglII - SmaI片段中的SSO处于错误的、无活性的方向,因此不能参与单链pSN22复制中间体向双链质粒形式的转化。我们发现这个BglII - SmaI片段包含两个SSO片段。对这两个SSO的二级结构分析显示与保守序列TAGCGT相似,该序列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。删除这些六核苷酸序列导致SSO活性丧失。我们的结果表明,两种类型的SSO,链霉菌型和葡萄球菌样型,可在淡紫链霉菌中发挥作用。

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