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The zinc finger protein cKrox directs CD4 lineage differentiation during intrathymic T cell positive selection

  1. Author:
    Sun, G. P.
    Liu, X. L.
    Mercado, P.
    Jenkinson, S. R.
    Kypriotou, M.
    Feigenbaum, L.
    Galera, P.
    Bosselut, R.
  2. Author Address

    Bosselut, R, NCI, Lab Immune Cell Biol, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Lab Immune Cell Biol, Ctr Canc Res, NIH, Bethesda, MD 20892 USA. CHU Caen, Fac Med, Lab Biochim Tissu Conjonctif, F-14000 Caen, France. NCI, Frederick Canc Res & Dev Ctr, Sci Applicat Int Corp, Frederick, MD 21702 USA.
    1. Year: 2005
  1. Journal: Nature Immunology
    1. 6
    2. 4
    3. Pages: 373-381
  2. Type of Article: Article
  1. Abstract:

    The genetic programs directing CD4 or CD8 T cell differentiation in the thymus remain poorly understood. While analyzing gene expression during intrathymic T cell selection, we found that Zfp67, encoding the zinc finger transcription factor cKrox, was upregulated during the differentiation of CD4(+) but not CD8(+) T cells. Expression of a cKrox transgene impaired CD8 T cell development and caused major histocompatibility complex class I - restricted thymocytes to differentiate into CD4(+) T cells with helper properties rather than into cytotoxic CD8(+) T cells, as normally found. CD4 lineage differentiation mediated by cKrox required its N-terminal BTB (bric-a-brac, tramtrack, broad complex) domain. These findings identify cKrox as a chief CD4 differentiation factor during positive selection

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External Sources

  1. WOS: 000227860000011

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