TY - JOUR
T1 - Regions of RAG1 protein critical for V(D)J recombination
AU - Kirch, Susan A.
AU - Sudarsanam, Priya
AU - Oettinger, Maijorie A.
N1 - Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
PY - 1996/4
Y1 - 1996/4
N2 - The products of the recombination activating genes RAG1 and RAG2 are essential for activating V(D)J recombination, and thus are indispensable for the production of functional and diverse antigen receptors. To investigate the function of RAG1, we have tested a series of insertion and substitution mutations for their ability to induce V(D)J rearrangement on both deletional and inversional plasmid substrates. With these substrates we were also able to assess the effects of these mutations on both coding and signal joint formation, and to show that any one mutant affected all these reactions similarly. As defined previously, the core active regions of RAG1 and RAG2 permit the deletion of 40% and 25%, respectively, of well-conserved sequence. We show here that this 'dispensable' region of RAG1 is not necessary for coding joint formation or for recombination of an integrated substrate, and that this portion is not functionally redundant with the 'dispensable' region of RAG2. Recombination with these core regions is also still subject to the 12/23 joining rule. Further, the minimal essential core region of RAG1 can be located within an even smaller portion of the gene.
AB - The products of the recombination activating genes RAG1 and RAG2 are essential for activating V(D)J recombination, and thus are indispensable for the production of functional and diverse antigen receptors. To investigate the function of RAG1, we have tested a series of insertion and substitution mutations for their ability to induce V(D)J rearrangement on both deletional and inversional plasmid substrates. With these substrates we were also able to assess the effects of these mutations on both coding and signal joint formation, and to show that any one mutant affected all these reactions similarly. As defined previously, the core active regions of RAG1 and RAG2 permit the deletion of 40% and 25%, respectively, of well-conserved sequence. We show here that this 'dispensable' region of RAG1 is not necessary for coding joint formation or for recombination of an integrated substrate, and that this portion is not functionally redundant with the 'dispensable' region of RAG2. Recombination with these core regions is also still subject to the 12/23 joining rule. Further, the minimal essential core region of RAG1 can be located within an even smaller portion of the gene.
KW - RAG1
KW - RAG2
KW - Site-directed mutagenesis
KW - V(D)J recombination
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U2 - 10.1002/eji.1830260425
DO - 10.1002/eji.1830260425
M3 - Article
C2 - 8625984
AN - SCOPUS:0029917808
SN - 0014-2980
VL - 26
SP - 886
EP - 891
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 4
ER -