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Coreceptor gene imprinting governs thymocyte lineage fate.

Stanley Adoro | Thomas McCaughtry | Batu Erman | Amala Alag | François Van Laethem | Jung-Hyun Park | Xuguang Tai | Motoko Kimura | Lie Wang | Alex Grinberg | Masato Kubo | Remy Bosselut | Paul Love | Alfred Singer
The EMBO journal | 2012

Immature thymocytes are bipotential cells that are signalled during positive selection to become either helper- or cytotoxic-lineage T cells. By tracking expression of lineage determining transcription factors during positive selection, we now report that the Cd8 coreceptor gene locus co-opts any coreceptor protein encoded within it to induce thymocytes to express the cytotoxic-lineage factor Runx3 and to adopt the cytotoxic-lineage fate, findings we refer to as 'coreceptor gene imprinting'. Specifically, encoding CD4 proteins in the endogenous Cd8 gene locus caused major histocompatibility complex class II-specific thymocytes to express Runx3 during positive selection and to differentiate into CD4(+) cytotoxic-lineage T cells. Our findings further indicate that coreceptor gene imprinting derives from the dynamic regulation of specific cis Cd8 gene enhancer elements by positive selection signals in the thymus. Thus, for coreceptor-dependent thymocytes, lineage fate is determined by Cd4 and Cd8 coreceptor gene loci and not by the specificity of T-cell antigen receptor/coreceptor signalling. This study identifies coreceptor gene imprinting as a critical determinant of lineage fate determination in the thymus.

Pubmed ID: 22036949

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Associated grants

  • Agency: Intramural NIH HHS, United States

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