Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A

Jian Xu, Daniel E. Bauer, Marc A. Kerenyi, Thuy D. Vo, Serena Hou, Yu Jung Hsu, Huilan Yao, Jennifer J. Trowbridge, Gail Mandel, Stuart H. Orkin

Research output: Contribution to journalArticle

90 Citations (Scopus)

Abstract

Reactivation of fetal hemoglobin (HbF) in adults ameliorates the severity of the common β-globin disorders. The transcription factor BCL11A is a critical modulator of hemoglobin switching and HbF silencing, yet the molecular mechanism through which BCL11A coordinates the developmental switch is incompletely understood. Particularly, the identities of BCL11A cooperating protein complexes and their roles in HbF expression and erythroid development remain largely unknown. Here we determine the interacting partner proteins of BCL11A in erythroid cells by a proteomic screen. BCL11A is found within multiprotein complexes consisting of erythroid transcription factors, transcriptional corepressors, and chromatin-modifying enzymes. We show that the lysine-specific demethylase 1 and repressor element-1 silencing transcription factor corepressor 1 (LSD1/CoREST) histone demethylase complex interacts with BCL11A and is required for full developmental silencing of mouse embryonic β-like globin genes and human γ-globin genes in adult erythroid cells in vivo. In addition, LSD1 is essential for normal erythroid development. Furthermore, the DNA methyltransferase 1 (DNMT1) is identified as a BCL11A-associated protein in the proteomic screen. DNMT1 is required to maintain HbF silencing in primary human adult erythroid cells. DNMT1 haploinsufficiency combined with BCL11A deficiency further enhances γ-globin expression in adult animals. Our findings provide important insights into the mechanistic roles of BCL11A in HbF silencing and clues for therapeutic targeting of BCL11A in β-hemoglobinopathies.

Original languageEnglish (US)
Pages (from-to)6518-6523
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume110
Issue number16
DOIs
StatePublished - Apr 16 2013

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Fetal Hemoglobin
Co-Repressor Proteins
Globins
Erythroid Cells
Methyltransferases
Transcription Factors
Proteomics
DNA
Histone Demethylases
Transcriptional Silencer Elements
Haploinsufficiency
Multiprotein Complexes
Hemoglobinopathies
Proteins
Genes
Lysine
Chromatin
Hemoglobins
Enzymes
Therapeutics

ASJC Scopus subject areas

  • General

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Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A. / Xu, Jian; Bauer, Daniel E.; Kerenyi, Marc A.; Vo, Thuy D.; Hou, Serena; Hsu, Yu Jung; Yao, Huilan; Trowbridge, Jennifer J.; Mandel, Gail; Orkin, Stuart H.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 110, No. 16, 16.04.2013, p. 6518-6523.

Research output: Contribution to journalArticle

Xu, J, Bauer, DE, Kerenyi, MA, Vo, TD, Hou, S, Hsu, YJ, Yao, H, Trowbridge, JJ, Mandel, G & Orkin, SH 2013, 'Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A', Proceedings of the National Academy of Sciences of the United States of America, vol. 110, no. 16, pp. 6518-6523. https://doi.org/10.1073/pnas.1303976110
Xu, Jian ; Bauer, Daniel E. ; Kerenyi, Marc A. ; Vo, Thuy D. ; Hou, Serena ; Hsu, Yu Jung ; Yao, Huilan ; Trowbridge, Jennifer J. ; Mandel, Gail ; Orkin, Stuart H. / Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A. In: Proceedings of the National Academy of Sciences of the United States of America. 2013 ; Vol. 110, No. 16. pp. 6518-6523.
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