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质粒pSC101复制的最小必需起始点:迭代子下游区域的需求。

Minimal essential origin of plasmid pSC101 replication: requirement of a region downstream of iterons.

作者信息

Sugiura S, Ohkubo S, Yamaguchi K

机构信息

Institute for Gene Research, Kanazawa University, Japan.

出版信息

J Bacteriol. 1993 Sep;175(18):5993-6001. doi: 10.1128/jb.175.18.5993-6001.1993.

Abstract

The minimal replication origin (ori) of the plasmid pSC101 was defined as an about 220-bp region under the condition that the Rep (or RepA) protein, a plasmid-encoded initiator protein, was supplied in trans. The DnaA box is located at one end of ori, as in other plasmids, like mini-F and P1. The other border is a strong binding site (IR-1) of Rep which is palindromic sequence and lies in an about 50-bp region beyond the repeated sequences (iterons) in ori. This IR-1 is located just upstream of another strong Rep binding site (IR-2), the operator site of the structure gene of Rep (rep), but its function has not been determined. The present study shows that the IR-1 sequence capable of binding to Rep is essential for plasmid replication with a nearly normal copy number. Furthermore, a region between the third iteron and IR-1 is also required in a sequence-specific fashion, since some one-base substitution in this region inactivate the origin function. It is likely that the region also is a recognition site of an unknown protein. Three copy number mutations of rep can suppress any one-base substitution mutation. On the other hand, the sequence of a spacer region between the second and the third iterons, which is similar to that of the downstream region of the third iteron, can be changed without loss of the origin function. The requirement of the region downstream of iterons in pSC101 seems to be unique among iteron-driven plasmid replicons.

摘要

在反式提供质粒编码的起始蛋白Rep(或RepA)的条件下,质粒pSC101的最小复制起点(ori)被定义为一个约220bp的区域。与mini-F和P1等其他质粒一样,DnaA框位于ori的一端。另一个边界是Rep的强结合位点(IR-1),它是回文序列,位于ori中重复序列(迭代子)之外的约50bp区域内。这个IR-1位于Rep结构基因(rep)的另一个强结合位点(IR-2),即操纵位点的上游,但它的功能尚未确定。本研究表明,能够与Rep结合的IR-1序列对于具有近乎正常拷贝数的质粒复制至关重要。此外,第三个迭代子和IR-1之间的区域也以序列特异性方式被需要,因为该区域中的一些单碱基取代会使起点功能失活。该区域可能也是一种未知蛋白质的识别位点。rep的三个拷贝数突变可以抑制任何单碱基取代突变。另一方面,第二个和第三个迭代子之间的间隔区序列,与第三个迭代子的下游区域序列相似,可以改变而不丧失起点功能。pSC101中迭代子下游区域的需求在迭代子驱动的质粒复制子中似乎是独特的。

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