bioRxiv · 10.1101/861542
An Erg driven transcriptional program controls B-lymphopoiesis
Abstract
Summary/AbstractB-cell development is initiated by the stepwise differentiation of hematopoietic stem cells into lineage committed progenitors, ultimately generating the mature B-cells that mediate protective immunity. This highly regulated process also generates clonal immunological diversity via recombination of immunoglobulin genes. While several transcription factors that control B-cell development and V(D)J recombination have been defined, how these processes are initiated and coordinated into a precise regulatory network remains poorly understood. Here, we show that the transcription factor ETS Related Gene (Erg) is essential for the earliest steps in B-cell differentiation. Erg initiates a transcriptional network involving the B-cell lineage defining genes, Ebf1 and Pax5, that directly promotes the expression of key genes involved in V(D)J recombination and formation of the B-cell receptor. Complementation of the Erg-deficiency with a productively rearranged immunoglobulin gene rescued B-cell development, demonstrating that Erg is an essential and exquisitely stage specific regulator of the gene regulatory network controlling B-lymphopoiesis.
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Ng, A. P., Coughlan, H. D., Hediyeh-zadeh, S., Behrens, K., Johanson, T. M., Low, M. S. Y., Bell, C. C., Gilan, O., Chan, Y.-C., Kueh, A. J., Boudier, T., DiRago, L., Hyland, C. D., Ierino, H., Mifsud, S., Viney, E., Willson, T., Dawson, M. A., Allan, R. S., Herold, M. J., Rogers, K., Tarlinton, D. M., Smyth, G., Davis, M. J., Nutt, S. L., Alexander, W. S.. 2019-12-03. An Erg driven transcriptional program controls B-lymphopoiesis. https://doi.org/10.1101/861542
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