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Journal of Bacteriology, February 2006, p. 999-1010, Vol. 188, No. 3
0021-9193/06/$08.00+0     doi:10.1128/JB.188.3.999-1010.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Anatomy of the Replication Origin of Plasmid ColE2-P9

Masaru Yagura,1 Shin-ya Nishio,1 Hideki Kurozumi,1 Cheng-fu Wang,1,{dagger} and Tateo Itoh1,2*

Department of Biology, Faculty of Science, Shinshu University, Matsumoto, Nagano 390-8621,1 Department of Biology, Faculty of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan2

Received 6 July 2005/ Accepted 3 November 2005

The plasmid ColE2-P9 origin is a 32-bp region which is specifically recognized by the plasmid-specified Rep protein to initiate DNA replication. We analyzed the structural and functional organization of the ColE2 origin by using various derivatives carrying deletions and single-base-pair substitutions. The origin may be divided into three subregions: subregion I, which is important for stable binding of the Rep protein; subregion II, which is important for binding of the Rep protein and for initiation of DNA replication; and subregion III, which is important for DNA replication but apparently not for binding of the Rep protein. The Rep protein might recognize three specific DNA elements in subregions I and II. The relative transformation frequency of the autonomously replicating plasmids carrying deletions in subregion I is lower, and nevertheless the copy numbers of these plasmids in host bacteria are higher than those of the wild-type plasmid. Efficient and stable binding of the Rep protein to the origin might be important for the replication efficiency to be at the normal (low) level. Subregion II might be essential for interaction with the catalytic domain of the Rep protein for primer RNA synthesis. The 8-bp sequence across the border of subregions II and III, including the primer sequence, is conserved in the (putative) origins of many plasmids, the putative Rep proteins of which are related to the ColE2-P9 Rep protein. Subregion III might be required for a step that is necessary after Rep protein binding has taken place.

* Corresponding author. Mailing address: Department of Biology, Faculty of Science, Shinshu University, Matsumoto, Nagano 390-8621, Japan. Phone: 81-263-37-2489. Fax: 81-263-37-2560. E-mail: tateito{at}gipac.shinshu-u.ac.jp.

{dagger} Present address: Department of Biochemistry, Suzhou Medical College, Suzhou, Jiangsu 215007, People's Republic of China.

Journal of Bacteriology, February 2006, p. 999-1010, Vol. 188, No. 3
0021-9193/06/$08.00+0     doi:10.1128/JB.188.3.999-1010.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Chatterjee, S., Basu, A., Basu, A., Das Gupta, S. K. (2007). DNA Bending in the Mycobacterial Plasmid pAL5000 Origin-RepB Complex. J. Bacteriol. 189: 8584-8592 [Abstract] [Full Text]  
  • Aoki, K., Shinohara, M., Itoh, T. (2007). Distinct Functions of the Two Specificity Determinants in Replication Initiation of Plasmids ColE2-P9 and ColE3-CA38. J. Bacteriol. 189: 2392-2400 [Abstract] [Full Text]  
  • Han, M., Yagura, M., Itoh, T. (2007). Specific Interaction between the Initiator Protein (Rep) and Origin of Plasmid ColE2-P9. J. Bacteriol. 189: 1061-1071 [Abstract] [Full Text]  


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