Literature DB >> 17224162

Systematic RNAi studies on the role of Sp/KLF factors in globin gene expression and erythroid differentiation.

Jie Hong Hu1, Patrick Navas, Hua Cao, George Stamatoyannopoulos, Chao-Zhong Song.   

Abstract

Sp/KLF family of factors regulates gene expression by binding to the CACCC/GC/GT boxes in the DNA through their highly conserved three zinc finger domains. To investigate the role of this family of factors in erythroid differentiation and globin gene expression, we first measured the expression levels of selected Sp/KLF factors in primary cells of fetal and adult stages of erythroid development. This quantitative analysis revealed that their expression levels vary significantly in cells of either stages of the erythroid development. Significant difference in their expression levels was observed between fetal and adult erythroid cells for some Sp/KLF factors. Functional studies using RNA interference revealed that the silencing of Sp1 and KLF8 resulted in elevated level of gamma globin expression in K562 cells. In addition, K562 cells become visibly red after Sp1 knockdown. Benzidine staining revealed significant hemoglobinization of these cells, indicating erythroid differentiation. Moreover, the expression of PU.1, ETS1 and Notch1 is significantly down-regulated in the cells that underwent erythroid differentiation following Sp1 knockdown. Overexpression of PU.1 or ETS1 efficiently blocked the erythroid differentiation caused by Sp1 knockdown in K562 cells. The expression of c-Kit, however, was significantly up-regulated. These data indicate that Sp1 may play an important role in erythroid differentiation.

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Year:  2006        PMID: 17224162      PMCID: PMC1907364          DOI: 10.1016/j.jmb.2006.12.047

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  38 in total

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2.  Deregulated expression of the PU.1 transcription factor blocks murine erythroleukemia cell terminal differentiation.

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Journal:  Oncogene       Date:  1997-01-09       Impact factor: 9.867

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Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

4.  A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Krüppel family of nuclear proteins.

Authors:  I J Miller; J J Bieker
Journal:  Mol Cell Biol       Date:  1993-05       Impact factor: 4.272

5.  Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF.

Authors:  A C Perkins; A H Sharpe; S H Orkin
Journal:  Nature       Date:  1995-05-25       Impact factor: 49.962

6.  Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF gene.

Authors:  B Nuez; D Michalovich; A Bygrave; R Ploemacher; F Grosveld
Journal:  Nature       Date:  1995-05-25       Impact factor: 49.962

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Authors:  Natasha Rekhtman; Kevin S Choe; Igor Matushansky; Stuart Murray; Tomas Stopka; Arthur I Skoultchi
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Authors:  D Donze; T M Townes; J J Bieker
Journal:  J Biol Chem       Date:  1995-01-27       Impact factor: 5.157

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Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-30       Impact factor: 11.205

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3.  Krüppel-like Factor 4 activates HBG gene expression in primary erythroid cells.

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6.  A feedback loop consisting of microRNA 23a/27a and the β-like globin suppressors KLF3 and SP1 regulates globin gene expression.

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Journal:  Mol Cell Biol       Date:  2013-08-05       Impact factor: 4.272

7.  KLF8 recruits the p300 and PCAF co-activators to its amino terminal activation domain to activate transcription.

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10.  Erythroid induction of K562 cells treated with mithramycin is associated with inhibition of raptor gene transcription and mammalian target of rapamycin complex 1 (mTORC1) functions.

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