Abstract
The T cell receptor (TCR) σ locus lies within the TCR α locus and is excised from the chromosome by Vα-Jα rearrangement. We show here that σ sequences persist in a large fraction of the DNA from mature CD4 +CD8 −αβ + mouse thymocytes. Virtually all σ loci in these cells are rearranged and present in extrachromosomal DNA. In immature αβ lineage thymocytes (CD3 −/loCD4 +CD8 +) and in CD4 +CDS −αβ + thymocytes expressing a transgene-encoded αβ receptor, rearranged σ genes are present both in chromosomal and extrachromosomal DNA. Thus, contrary to earlier proposals, commitment to the αβ lineage does not require recombinational silencing of the σ locus or its deletion by a site-specific mechanism prior to Vα-Jα rearrangement.
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