An extrachromosomal switch recombination substrate reveals kinetics and substrate requirements of switch recombination in primary murine B cells
Author(s) -
Katja Petry,
Gregor Siebenkotten,
Rainer Christine,
Katharina Hein,
Andreas Radbruch
Publication year - 1999
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/11.5.753
Subject(s) - immunoglobulin class switching , recombination , microbiology and biotechnology , site specific recombination , extrachromosomal dna , cre lox recombination , biology , cre recombinase , flp frt recombination , transfection , primary cell , chemistry , recombinase , b cell , genetics , gene , genetic recombination , transgene , antibody , plasmid , genetically modified mouse
Ig class switch recombination occurs in B lymphocytes upon activation, and is targeted to distinct switch (S) regions by cytokine-mediated induction of switch transcripts spanning the entire S region and the adjacent constant region gene segments. Using a novel type of switch recombination substrate, constructed according to the intron-exon structure of the IgH locus, but with heterologous elements, we here have tested the structural requirements for targeting and the kinetics of switch recombination in activated primary murine B cells. When transfected at various times after activation, up to 10% of the transfected B cells perform recombination of the substrate within 12 h. Switch recombination in primary B cells is restricted to the first 72 h after onset of activation, then rapidly decreases to background levels, as obtained in plasmacytoma cells or with substrates carrying no S region sequences. In terms of structural requirements, switch recombination is targeted to any transcription unit that contains an intronic S region and depends on processing of the primary transcript by splicing.
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