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Nat Immunol. 2014 Dec;15(12):1171-80. doi: 10.1038/ni.3024. Epub 2014 Oct 26.

The transcription repressors Bach2 and Bach1 promote B cell development by repressing the myeloid program.

Author information

1
1] Department of Biochemistry, Tohoku University Graduate School of Medicine, Sendai, Japan. [2] CREST, Japan Science and Technology Agency, Sendai, Japan.
2
Department of Biochemistry, Tohoku University Graduate School of Medicine, Sendai, Japan.
3
RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
4
Department of Cellular Biology, Research Institute for Radiation Biology and Medicine, Graduate School of Biomedical Science, Hiroshima University, Hiroshima, Japan.
5
Laboratory for Immune Regeneration RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
6
1] Department of Biochemistry, Tohoku University Graduate School of Medicine, Sendai, Japan. [2] CREST, Japan Science and Technology Agency, Sendai, Japan. [3] Center for Regulatory Epigenome and Diseases, Tohoku University Graduate School of Medicine, Sendai, Japan.
7
1] RIKEN Center for Integrative Medical Sciences, Yokohama, Japan. [2] WPI Immunology Frontier Research Center, Osaka University, Suita, Japan.

Abstract

Mature lymphoid cells express the transcription repressor Bach2, which imposes regulation on humoral and cellular immunity. Here we found critical roles for Bach2 in the development of cells of the B lineage, commencing from the common lymphoid progenitor (CLP) stage, with Bach1 as an auxiliary. Overexpression of Bach2 in pre-pro-B cells deficient in the transcription factor EBF1 and single-cell analysis of CLPs revealed that Bach2 and Bach1 repressed the expression of genes important for myeloid cells ('myeloid genes'). Bach2 and Bach1 bound to presumptive regulatory regions of the myeloid genes. Bach2(hi) CLPs showed resistance to myeloid differentiation even when cultured under myeloid conditions. Our results suggest that Bach2 functions with Bach1 and EBF1 to promote B cell development by repressing myeloid genes in CLPs.

PMID:
25344725
DOI:
10.1038/ni.3024
[Indexed for MEDLINE]

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