Transcription factors regulate early T cell development via redeployment of other factors: Functional dynamics of constitutively required factors in cell fate decisions
- PMID: 33624856
- DOI: 10.1002/bies.202000345
Transcription factors regulate early T cell development via redeployment of other factors: Functional dynamics of constitutively required factors in cell fate decisions
Abstract
Establishment of cell lineage identity from multipotent progenitors is controlled by cooperative actions of lineage-specific and stably expressed transcription factors, combined with input from environmental signals. Lineage-specific master transcription factors activate and repress gene expression by recruiting consistently expressed transcription factors and chromatin modifiers to their target loci. Recent technical advances in genome-wide and multi-omics analysis have shed light on unexpected mechanisms that underlie more complicated actions of transcription factors in cell fate decisions. In this review, we discuss functional dynamics of stably expressed and continuously required factors, Notch and Runx family members, throughout developmental stages of early T cell development in the thymus. Pre- and post-commitment stage-specific transcription factors induce dynamic redeployment of Notch and Runx binding genomic regions. Thus, together with stage-specific transcription factors, shared transcription factors across distinct developmental stages regulate acquisition of T lineage identity.
Keywords: Notch signal; Runx factors; cell fate decision; early T cell development; stage-specific action; transcription factor network.
© 2021 Wiley Periodicals LLC.
References
REFERENCES
-
- Chronis, C., Fiziev, P., Papp, B., Butz, S., Bonora, G., Sabri, S., Ernst, J., & Plath, K. (2017). Cooperative binding of transcription factors orchestrates reprogramming. Cell, 168(3), 442-59.e20. https://doi.org/10.1016/j.cell.2016.12.016
-
- Takahashi, K., & Yamanaka, S. (2016). A decade of transcription factor-mediated reprogramming to pluripotency. Nature Reviews Molecular Cell Biology, 17(3), 183-193. https://doi.org/10.1038/nrm.2016.8
-
- Cai, Z., De Bruijn, M., Ma, X., Dortland, B., Luteijn, T., Downing, J. R., & Dzierzak, E. (2000). Haploinsufficiency of AML1 affects the temporal and spatial generation of hematopoietic stem cells in the mouse embryo. Immunity, 13(4), 423-431. https://doi.org/10.1016/s1074-7613(00)00042-x
-
- Rodrigues, N. P. (2005). Haploinsufficiency of GATA-2 perturbs adult hematopoietic stem-cell homeostasis. Blood, 106(2), 477-484. https://doi.org/10.1182/blood-2004-08-2989
-
- Talebian, L., Li, Z., Guo, Y., Gaudet, J., Speck, M. E., Sugiyama, D., Kaur, P., Pear, W. S., Maillard, I., & Speck, N. A. (2007). T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFbeta dosage. Blood, 109(1), 11-21. https://doi.org/10.1182/blood-2006-05-021188
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
