JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kahn, R.
Right arrow Articles by Radding, C. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kahn, R.
Right arrow Articles by Radding, C. M.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

J. Biol. Chem., Vol. 259, Issue 12, 7495-7503, Jun, 1984

Separation of the presynaptic and synaptic phases of homologous pairing promoted by recA protein

R Kahn and CM Radding

Homologous pairing of single strands with duplex DNA promoted by recA protein occurred without a lag only when the protein was preincubated with ATP and single-stranded DNA. The rate-limiting presynaptic interaction of recA protein and single strands showed a high temperature coefficient: it proceeded 30 times more slowly at 30 degrees C than at 37 degrees C, whereas synapsis showed a normal temperature coefficient. Thus, the presynaptic phase could be separated experimentally from the rest of the reaction by preincubation of single strands with recA protein and ATP at 37 degrees C, followed by a shift to 30 degrees C before double-stranded DNA was added. The presynaptic phase was an order of magnitude more sensitive to inhibition by ADP than was subsequent strand exchange. Presynaptic complexes that were formed at 37 degrees C decayed only slowly at 30 degrees C, but Escherichia coli single strand binding protein caused complexes to form rapidly at 30 degrees C which indicates that single strand binding protein accelerated the rate of formation of complexes. Preincubation synchronized the initial pairing reaction, and further revealed the rapid formation of nascent heteroduplex DNA 250-300 base pairs in length.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
T. Shibata, T. Nishinaka, T. Mikawa, H. Aihara, H. Kurumizaka, S. Yokoyama, and Y. Ito
Homologous genetic recombination as an intrinsic dynamic property of a DNA structure induced by RecA/Rad51-family proteins: A possible advantage of DNA over RNA as genomic material
PNAS, July 17, 2001; 98(15): 8425 - 8432.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
T. Nishinaka, A. Shinohara, Y. Ito, S. Yokoyama, and T. Shibata
Base pair switching by interconversion of sugar puckers in DNA extended by proteins of RecA-family: A model for homology search in homologous genetic recombination
PNAS, September 15, 1998; 95(19): 11071 - 11076.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Q. Shan and M. M. Cox
RecA Filament Dynamics during DNA Strand Exchange Reactions
J. Biol. Chem., April 25, 1997; 272(17): 11063 - 11073.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
H. Kurumizaka, H. Aihara, S. Ikawa, T. Kashima, L. R. Bazemore, K. Kawasaki, A. Sarai, C. M. Radding, and T. Shibata
A Possible Role of the C-terminal Domain of the RecA Protein. A GATEWAY MODEL FOR DOUBLE-STRANDED DNA BINDING
J. Biol. Chem., December 27, 1996; 271(52): 33515 - 33524.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Q. Shan, M. M. Cox, and R. B. Inman
DNA Strand Exchange Promoted by RecA K72R
J. Biol. Chem., March 8, 1996; 271(10): 5712 - 5724.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
F. Salinas, H. Jiang, and T. Kodadek
Homology Dependence of UvsX Protein-catalyzed Joint Molecule Formation
J. Biol. Chem., March 10, 1995; 270(10): 5181 - 5186.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. G. Thomas, T. B. Thompson, I. Rayment, and J. C. Escalante-Semerena
Analysis of the Adenosylcobinamide Kinase/Adenosylcobinamide-phosphate Guanylyltransferase (CobU) Enzyme of Salmonella typhimurium LT2. IDENTIFICATION OF RESIDUE His-46 AS THE SITE OF GUANYLYLATION
J. Biol. Chem., September 1, 2000; 275(36): 27576 - 27586.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1984 by the American Society for Biochemistry and Molecular Biology.