Abstract
We show that knockdown of KLF1 in human and mouse adult erythroid progenitors markedly reduces BCL11A levels and increases human γ-globin/β-globin expression ratios. These results suggest that KLF1 controls globin gene switching by directly activating β-globin and indirectly repressing γ-globin gene expression. Controlled knockdown of KLF1 in adult erythroid progenitors may provide a method to activate fetal hemoglobin expression in individuals with β-thalassemia or sickle cell disease.
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Change history
24 October 2010
In the version of this supplementary file originally posted online, there were several lines missing from the schematic drawings in Supplementary Figures 2–4. The errors have been corrected in this file as of 24 September 2010.
References
Zhou, D., Pawlik, K.M., Ren, J., Sun, C.W. & Townes, T.M. J. Biol. Chem. 281, 16052–16057 (2006).
Xue, L., Chen, X., Chang, Y. & Bieker, J.J. Blood 103, 4078–4083 (2004).
Lettre, G. et al. Proc. Natl. Acad. Sci. USA 105, 11869–11874 (2008).
Sankaran, V.G. et al. Science 322, 1839–1842 (2008).
Sankaran, V.G. et al. Nature 460, 1093–1097 (2009).
Xu, J. et al. Genes Dev. 24, 783–798 (2010).
Behringer, R.R., Ryan, T.M., Palmiter, R.D., Brinster, R.L. & Townes, T.M. Genes Dev. 4, 380–389 (1990).
Carter, D., Chakalova, L., Osborne, C.S., Dai, Y.F. & Fraser, P. Nat. Genet. 32, 623–626 (2002).
Donze, D., Townes, T.M. & Bieker, J.J. J. Biol. Chem. 270, 1955–1959 (1995).
Drissen, R. et al. Genes Dev. 18, 2485–2490 (2004).
Enver, T. et al. Nature 344, 309–313 (1990).
Perkins, A.C., Gaensler, K.M. & Orkin, S.H. Proc. Natl. Acad. Sci. USA 93, 12267–12271 (1996).
Ryan, T.M., Sun, C.W., Ren, J. & Townes, T.M. Nucleic Acids Res. 28, 2736–2740 (2000).
Tewari, R. et al. EMBO J. 17, 2334–2341 (1998).
Townes, T.M. & Behringer, R.R. Trends Genet. 6, 219–223 (1990).
Acknowledgements
We thank L. Lamb for purification of CD34+ cells from mobilized peripheral blood mononuclear cells, T. Ley for the human β-globin BAC and S. McConnell for help with qRT-PCR. This work was supported by a grant from the US National Institutes of Health (1R01 DK073391).
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All authors contributed to the design of the experiments and to the writing of the paper. D.Z. produced the Klf1 ESH1Δ mice and performed most of the experiments. K.L. prepared the lentiviral shRNA viruses. C.-W.S. prepared the E10.5 yolk sac cells. K.M.P. contributed to the ChIP experiments.
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Supplementary Figures 1–6 and Supplementary Methods (PDF 648 kb)
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Zhou, D., Liu, K., Sun, CW. et al. KLF1 regulates BCL11A expression and γ- to β-globin gene switching. Nat Genet 42, 742–744 (2010). https://doi.org/10.1038/ng.637
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DOI: https://doi.org/10.1038/ng.637
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