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Original Article |
Correspondence to: Erik Selsing, Department of Pathology, Tufts University School of Medicine, Boston, MA 02111. Tel:617-636-0467 Fax:617-636-6903 E-mail:eselsing{at}opal.tufts.edu.
Class switch DNA recombinations change the constant (C) region of the antibody heavy (H) chain expressed by a B cell and thereby change the antibody effector function. Unusual tandemly repeated sequence elements located upstream of H chain gene exons have long been thought to be important in the targeting and/or mechanism of the switch recombination process. We have deleted the entire switch tandem repeat element (Sµ) from the murine µ H chain gene. We find that the Sµ tandem repeats are not required for class switching in the mouse immunoglobulin H-chain locus, although the efficiency of switching is clearly reduced. Our data demonstrate that sequences outside of the Sµ tandem repeats must be capable of directing the class switch mechanism. The maintenance of the highly repeated Sµ element during evolution appears to reflect selection for a highly efficient switching process rather than selection for a required sequence element.
Key Words: gene rearrangement, B lymphocyte, heavy chain, class switching, immunoglobulin isotype
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