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Sequence Analysis of the Mouse RAG Locus lntergenic Region
Author(s) -
F. E. Bertrand,
S. L. Olsona,
Danielle Martin,
Guang-fu Wu
Publication year - 1997
Publication title -
journal of immunology research
Language(s) - English
Resource type - Journals
eISSN - 2314-8861
pISSN - 2314-7156
DOI - 10.1155/1998/54045
Subject(s) - biology , locus (genetics) , genetics , gene , transcription (linguistics) , recombination signal sequences , microbiology and biotechnology , gene rearrangement , open reading frame , recombination activating gene , peptide sequence , recombination , linguistics , philosophy
The recombination activating genes RAG-1 and RAG-2 are highly conserved throughout evolution and are necessary and essential for the DNA rearrangement of antigen-receptor gene segments. These convergently transcribed genes are expressed primarily by developing B and T lineage cells. In addition, recent data suggest that the RAG locus can be reactivated in mouse germinal center B cells. Despite these well-defined patterns of expression, little is known about mechanism(s) regulating transcription of the RAG locus. Experiments with a mouse fibroblast line stably transfected with a genomic fragment of the RAG locus suggest that the intergenic region between RAG-1 and RAG-2 may contain information modulating RAG transcription. In order to begin testing this hypothesis, we have sequenced the 7.0-kb RAG intergenic region of the mouse. The sequence did not contain open reading frames larger than 60 amino acids. Analysis with GCG software identified several potential transcription-factor binding sequences within this region. Many of these are associated with transcriptional regulation of the Ig locus.

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