BCL11B is positioned upstream of PLZF and RORγt to control thymic development of mucosal-associated invariant T cells and MAIT17 program

Theodore T. Drashansky, Eric Y. Helm, Nina Curkovic, Jaimee Cooper, Pingyan Cheng, Xianghong Chen, Namrata Gautam, Lingsong Meng, Alexander J. Kwiatkowski, William O. Collins, Benjamin G. Keselowsky, Derek Sant'Angelo, Zhiguang Huo, Weizhou Zhang, Liang Zhou, Dorina Avram

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Mucosal-associated invariant T (MAIT) cells recognize microbial riboflavin metabolites presented by MR1 and play role in immune responses to microbial infections and tumors. We report here that absence of the transcription factor (TF) Bcl11b in mice alters predominantly MAIT17 cells in the thymus and further in the lung, both at steady state and following Salmonella infection. Transcriptomics and ChIP-seq analyses show direct control of TCR signaling program and position BCL11B upstream of essential TFs of MAIT17 program, including RORγt, ZBTB16 (PLZF), and MAF. BCL11B binding at key MAIT17 and at TCR signaling program genes in human MAIT cells occurred mostly in regions enriched for H3K27Ac. Unexpectedly, in human MAIT cells, BCL11B also bound at MAIT1 program genes, at putative active enhancers, although this program was not affected in mouse MAIT cells in the absence of Bcl11b. These studies endorse BCL11B as an essential TF for MAIT cells both in mice and humans.

Original languageEnglish (US)
Article number102307
JournaliScience
Volume24
Issue number4
DOIs
StatePublished - Apr 23 2021

All Science Journal Classification (ASJC) codes

  • General

Keywords

  • Immunology
  • Systems Biology
  • Transcriptomics

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