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Issue 850 coverCOOLEY'S ANEMIA: SEVENTH SYMPOSIUM Copyright © 1998 by the New York Academy of Sciences
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Articles by GINDER, G. D.
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Annals of the New York Academy of Sciences 850:70-79 (1998)
© 1998 New York Academy of Sciences

Silencing and Activation of Embryonic Globin Gene Expression

GORDON D. GINDERa-e, RAKESH SINGALa,b, JANE A. LITTLEa,b,d, NANCY DEMPSEYa,b, RICHARD FERRISa,b AND SHOU ZHEN WANGa,b,d

aDivision of Oncology, University of Minnesota, Minneapolis, Minnesota, USA
bDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, USA
cInstitute of Human Genetics, University of Minnesota, Minneapolis, Minnesota, USA
dCancer Center, University of Minnesota, Minneapolis, Minnesota, USA

eAddress correspondence to: Gordon D. Ginder, M.D., Professor of Internal Medicine and Human Genetics, Director, Massey Cancer Center, Virginia Commonwealth University, 401 College Street, P. O. Box 980037, Richmond, VA 23298-0037; Tel: (804) 828-0450; Fax: (804) 828-8453; E-mail: gginder{at}mcc1.mcc.vcu.edu

An understanding of the mechanisms that control developmental stage-specific transcription of globin genes offers the promise of successful therapeutic activation of fetal or embryonic ß-type genes in ß-thalassemia syndromes. A large body of evidence supports the notion of conservation of such mechanisms across vertebrate species and validates the use of pre-clinical studies of silencing and activation of fetal or embryonic globin genes in animals. Using globin gene transfections into primary avian erythroid cells and cultured murine erythroleukemia cells, we have studied mechanisms involved in stage-specific embryonic ß-type globin gene silencing and activation. These studies show that 1) methylation of the exact CpG nucleotides that are methylated in normal adult erythroid cells in vivo is capable of blocking transcription of a transfected embryonic globin gene promoter via binding of a methyl DNA binding protein in primary erythroid cells. 2) Activation of embryonic ß-type globin gene transcription in adult erythroid cells by short chain fatty acids is mediated through specific DNA sequences both in the promoter and downstream of the promoter.




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