Skip Navigation

This Article
Right arrow Print PDF (2632K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Wang, J. C.
Right arrow Articles by Becherer, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, J. C.
Right arrow Articles by Becherer, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1983, Vol. 11, No. 6 1773-1790
© 1983


MOLECULAR BIOLOGY

Cloning of the gene topA encoding for DNA topoisomerase 1 and the physical mapping of the cysB–topA–trpAregion of Escherichia colt

James C. Wang and Kathleen Becherer

Department of Biochemistry and Molecular Biology, Harvard University Cambridge, MA 02138, USA

Received January 5, 1983. Accepted February 10, 1983.

The gene topA of Escherichia coli that encodes for DNA topoisomerase I has been cloned by a combination of genetic and radioimmunal screening. The gene has been mapped to be within a 3.4 Kb segment of the bacterial genome. The intracellular level of the enzyme in strains harboring extra chromosomal copies of topA gene increases with increasing copy number of the gene and the introduction of extra chromosomal copies of the topA gene truncated at its 3’ side into a topA strain of E. coli does not significantly influence the expression of the chromosomal copy oftopA. These results suggest that the expression of topA is not tightly regulated. Strains in which DNA topoisomerase I is overproduced grow significantly slower in broth and give smaller size colonies on agar plates. Physical mapping of a 20 Kb region containing cysB; topA and trpA has also been carried out with a number of restriction enzymes; topA is found to be immediately adjacent to cysB and is separated from trpA by a 7 Kb segment where no known gene resides.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
V. A. Stupina and J. C. Wang
Viability of Escherichia coli topA Mutants Lacking DNA Topoisomerase I
J. Biol. Chem., January 7, 2005; 280(1): 355 - 360.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
M. K. B. Berlyn
Linkage Map of Escherichia coli K-12, Edition 10: The Traditional Map
Microbiol. Mol. Biol. Rev., September 1, 1998; 62(3): 814 - 984.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
E. Fritz, S. H. Elsea, P. I. Patel, and M. S. Meyn
Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype
PNAS, April 29, 1997; 94(9): 4538 - 4542.
[Abstract] [Full Text] [PDF]


Home page
J Biomol ScreenHome page
C. G. Lerner, A. Y. C. Saiki, A. C. Mackinnon, and X. Xuei
High Throughput Screen for Inhibitors of Bacterial DNA Topoisomerase I Using the Scintillation Proximity Assay
J Biomol Screen, April 1, 1996; 1(3): 135 - 143.
[Abstract] [PDF]


Home page
ScienceHome page
C. Smith, J. Econome, A Schutt, S Klco, and C. Cantor
A physical map of the Escherichia coli K12 genome
Science, June 12, 1987; 236(4807): 1448 - 1453.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
Y. Wang, A. S. Lynch, S.-J. Chen, and J. C. Wang
On the Molecular Basis of the Thermal Sensitivity of an Escherichia coli topA Mutant
J. Biol. Chem., January 4, 2002; 277(2): 1203 - 1209.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.