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Gene expression in mature CD4 and CD8 from WT mice and mature CD4 from DBTBLZ or Mta2-DBTBLZ retrogenic mice

ABSTRACT: T cell precursors develop into cytotoxic CD8 and helper CD4+ T cells in thymus. Thpok, a BTB/POZ family transcription factor, enforces commitment to the CD4 lineage and suppresses cytotoxic gene expression. However, it is still not fully understood how Thpok directs CD4 T cell development. Here, using mass-spectrometry, we identify nucleosome remodeling and deacetylase (NuRD) complex as a novel Thpok cofactor. We demonstrate that the Thpok BTB domain is essential for NuRD recruitment. Reconstituting NuRD binding to a BTB-less version of Thpok (which cannot bind NuRD) restored CD4 T cell in vivo. RNA sequencing showed that CD4 T cells expressing the reconstituted protein express a transcriptome similar to that of CD4 T cells expressing Thpok. Thus, our results demonstrate that NuRD recruitment is both necessary and sufficient for the function of the Thpok BTB domain in CD4 T cell development.

ORGANISM(S): Mus musculus

PROVIDER: GSE171610 | GEO | 2022/06/10

REPOSITORIES: GEO

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NuRD complex recruitment to Thpok mediates CD4+ T cell lineage differentiation

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NuRD complex recruitment to Thpok mediates CD4+ T cell lineage differentiation

Project description:NuRD complex recruitment to Thpok mediates CD4+ T cell lineage differentiation

| PRJNA821414 | ENA

Transcriptional changes in intraepithelial CD4 lymphocytes

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| MSV000088126 | MassIVE

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