Abstract:
:Previous in vitro studies defined the minimal regions of RAG1 and RAG2 essential for V(D)J recombination. In order to characterize the role of the C-terminal "dispensable" portion of RAG2, we generated core-RAG2 knock-in mice. We found that the core-RAG2-containing recombinase complex is selectively defective in catalyzing V-to-DJ rearrangement at the IgH and TCRbeta loci, resulting in partial developmental blocks in B and T lymphopoiesis. Analysis of recombination intermediates showed defects at the cleavage phase of the reaction. We also observed a reduction in overall recombinase activity in core-RAG2-expressing thymocytes, leading us to suggest that the interaction of a defective recombinase with RSS sequences unique to VH and Vbeta gene segments may underlie the specific V-to-DJ rearrangement defect in core-RAG2 mice.
journal_name
Immunityjournal_title
Immunityauthors
Liang HE,Hsu LY,Cado D,Cowell LG,Kelsoe G,Schlissel MSdoi
10.1016/s1074-7613(02)00448-xkeywords:
subject
Has Abstractpub_date
2002-11-01 00:00:00pages
639-51issue
5eissn
1074-7613issn
1097-4180pii
S1074-7613(02)00448-Xjournal_volume
17pub_type
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