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Molecular and Cellular Biology, March 2001, p. 2038-2047, Vol. 21, No. 6
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.6.2038-2047.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
A C-Terminal Region of RAG1 Contacts the Coding DNA
during V(D)J Recombination
Xianming
Mo,
Tu
Bailin, and
Moshe J.
Sadofsky*
Institute of Molecular Medicine and Genetics,
Medical College of Georgia, Augusta, Georgia 30912
Received 15 November 2000/Returned for modification 18 December
2000/Accepted 28 December 2000
The site-specific DNA rearrangement process, called V(D)J
recombination, creates much of the diversity of immune receptor molecules in the adaptive immune system. Central to this reaction is
the organization of the protein-DNA complex containing the proteins
RAG1 and RAG2 and their DNA targets. A long-term goal is to appreciate
the three-dimensional relationships between the proteins and DNA that
allow the assembly of the appropriate reaction intermediates, resulting
in concerted cleavage and directed rejoining of the DNA ends. Previous
cross-linking approaches have mapped RAG1 contacts on the DNA. RAG1
protein contacts the DNA at the conserved heptamer and nonamer
sequences as well as at the coding DNA adjacent to the heptamer. Here
we subject RAG1, covalently cross-linked to DNA substrates, to partial
cyanogen bromide degradation or trypsin proteolysis in order to map
contacts on the protein. We find that coding-sequence contacts occur
near the C terminus of RAG1, while contacts made within the
recombination signal sequence occur nearer the N terminus of the core
region of RAG1. A deletion protein lacking the C-terminal
DNA-contacting region is still capable of making the N-terminal
contacts. This suggests that the two binding interactions may exist on
two separate domains of the protein. A trypsin cleavage pattern of the
native protein supports this conclusion. A two-domain model for RAG1 is
evaluated with respect to the larger recombination complex.
*
Corresponding author. Mailing address: Medical College
of Georgia, Institute of Molecular Medicine and Genetics, CB-2803, Augusta, GA 30912. Phone: (706) 721-8761. Fax: (706) 721-8752. E-mail:
moshe{at}immag.mcg.edu.
Molecular and Cellular Biology, March 2001, p. 2038-2047, Vol. 21, No. 6
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.6.2038-2047.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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