Zinc finger protein Zfp335 is required for the formation of the naïve T cell compartment

BY Han, S Wu, CS Foo, RM Horton, CN Jenne… - Elife, 2014 - elifesciences.org
BY Han, S Wu, CS Foo, RM Horton, CN Jenne, SR Watson, B Whittle, CC Goodnow
Elife, 2014elifesciences.org
The generation of naïve T lymphocytes is critical for immune function yet the mechanisms
governing their maturation remain incompletely understood. We have identified a mouse
mutant, bloto, that harbors a hypomorphic mutation in the zinc finger protein Zfp335. Zfp335
bloto/bloto mice exhibit a naïve T cell deficiency due to an intrinsic developmental defect that
begins to manifest in the thymus and continues into the periphery, affecting T cells that have
recently undergone thymic egress. The effects of Zfp335bloto are multigenic and cannot be …
The generation of naïve T lymphocytes is critical for immune function yet the mechanisms governing their maturation remain incompletely understood. We have identified a mouse mutant, bloto, that harbors a hypomorphic mutation in the zinc finger protein Zfp335. Zfp335bloto/bloto mice exhibit a naïve T cell deficiency due to an intrinsic developmental defect that begins to manifest in the thymus and continues into the periphery, affecting T cells that have recently undergone thymic egress. The effects of Zfp335bloto are multigenic and cannot be attributed to altered thymic selection, proliferation or Bcl2-dependent survival. Zfp335 binds to promoter regions via a consensus motif, and its target genes are enriched in categories related to protein metabolism, mitochondrial function, and transcriptional regulation. Restoring the expression of one target, Ankle2, partially rescues T cell maturation. These findings identify Zfp335 as a transcription factor and essential regulator of late-stage intrathymic and post-thymic T cell maturation.
DOI: http://dx.doi.org/10.7554/eLife.03549.001
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