Modification of octamer binding transcriptional factor is related to H2B histone gene repression during dimethyl sulfoxide-dependent differentiation of HL-60 cells.

Lee MS; Son MY; Park JI; Park C; Lee YC; Son CB; Kim YS; Paik SG; Yoon WH; Park SK; Hwang BD; Lim K

doi:10.1016/s0304-3835(01)00654-1

Modification of octamer binding transcriptional factor is related to H2B histone gene repression during dimethyl sulfoxide-dependent differentiation of HL-60 cells.

Lee MS ¹,

Son MY ,

Park JI ,

Park C ,

Lee YC ,

Son CB ,

Kim YS ,

Affiliations

1. Department of Food & Nutrition, Chungnam National University, 305-764, Daejeon, South Korea.
Authors
Lee MS¹
(1 author)

ORCIDs linked to this article

Cancer Letters, 01 Oct 2001, 172(2):165-170
https://doi.org/10.1016/s0304-3835(01)00654-1 PMID: 11566492

Abstract

Transcriptional regulation of H2B histone gene during dimethyl sulfoxide (DMSO)-dependent differentiation of HL-60 cells has been investigated using DNase I footprinting and DNA mobility shift assay. The level of histone H2B mRNA showed a slight decline at 2 days and hardly detectable at 4 days after DMSO treatment. H2B histone mRNA was repressed in proportion to the concentration of DMSO. In DNase I footprinting analysis, one nuclear factor (octamer binding transcription factor, OTF) bound at -42 bp (octamer motif, ATTTGCAT) in undifferentiated HL-60 cells. The binding pattern of OTF was unchanged during DMSO-dependent differentiation. One protein complex (OTF) was detected by DNA mobility shift assay in undifferentiated HL-60 cells. The mobility of OTF was partially retarded during DMSO-dependent differentiation and the retardant OTF was not newly synthesized protein. These results suggest that the posttranslational modification of OTF may be responsible for the repression of H2B histone gene during DMSO-dependent differentiation of HL-60 cells.

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References

Articles referenced by this article (25)

Continuous growth and differentiation of human myeloid leukaemic cells in suspension culture.
Collins SJ, Gallo RC, Gallagher RE
Nature, (5635):347-349 1977
MED: 271272
Induction of morphological and functional differentiation of human promyelocytic leukemia cells (HL-60) by componuds which induce differentiation of murine leukemia cells.
Collins SJ, Bodner A, Ting R, Gallo RC
Int J Cancer, (2):213-218 1980
MED: 6156128
Terminal differentiation of human promyelocytic leukemia cells induced by dimethyl sulfoxide and other polar compounds.
Collins SJ, Ruscetti FW, Gallagher RE, Gallo RC
Proc Natl Acad Sci U S A, (5):2458-2462 1978
MED: 276884
Dimethylsulfoxide, retinoic acid 12-O-tetradecanoyl-phorbol-13-acetate induce a selective decrease in the phosphorylation of P150, a surface membrane phosphoprotein of HL-60 cells resistant to adriamycin
Marsh
Biochem. Biol. Res. Commun. 1986
The cytoplasmic synthesis of histones in hela cells and its temporal relationship to DNA replication.
Robbins E, Borun TW
Proc Natl Acad Sci U S A, (2):409-416 1967
MED: 16591485
Regulation of human histone gene expression: Kinetics of accumulation and changes in the rate of synthesis and half life of individual histone mRNAs during the HeLa cell cycle
Heintz
Mol. Cell. Biol. 1983
Histone mRNA concentrations are regulated at the level of transcription and mRNA degradation.
Sittman DB, Graves RA, Marzluff WF
Proc Natl Acad Sci U S A, (7):1849-1853 1983
MED: 6572946
Multilevel regulation of replication-dependent histone genes.
Schumperli D
Trends Genet, (7):187-191 1988
MED: 3070866
Cell-cycle regulatory sequences in a hamster histone promoter and their interactions with cellular factors.
Artishevsky A, Wooden S, Sharma A, Resendez E Jr, Lee AS
Nature, (6133):823-827 1987
MED: 3627229
Cell cycle regulation of a mouse histone H4 gene requires the H4 promoter.
Seiler-Tuyns A, Paterson BM
Mol Cell Biol, (3):1048-1054 1987
MED: 3561406

Show 10 more references (10 of 25)

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Modification of octamer binding transcriptional factor is related to H2B histone gene repression during dimethyl sulfoxide-dependent differentiation of HL-60 cells.

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Authors

ORCIDs linked to this article

Abstract

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References

Continuous growth and differentiation of human myeloid leukaemic cells in suspension culture.

Induction of morphological and functional differentiation of human promyelocytic leukemia cells (HL-60) by componuds which induce differentiation of murine leukemia cells.

Terminal differentiation of human promyelocytic leukemia cells induced by dimethyl sulfoxide and other polar compounds.

Dimethylsulfoxide, retinoic acid 12-O-tetradecanoyl-phorbol-13-acetate induce a selective decrease in the phosphorylation of P150, a surface membrane phosphoprotein of HL-60 cells resistant to adriamycin

The cytoplasmic synthesis of histones in hela cells and its temporal relationship to DNA replication.

Regulation of human histone gene expression: Kinetics of accumulation and changes in the rate of synthesis and half life of individual histone mRNAs during the HeLa cell cycle

Histone mRNA concentrations are regulated at the level of transcription and mRNA degradation.

Multilevel regulation of replication-dependent histone genes.

Cell-cycle regulatory sequences in a hamster histone promoter and their interactions with cellular factors.

Cell cycle regulation of a mouse histone H4 gene requires the H4 promoter.

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Citations of article over time

Smart citations by scite.ai
Explore citation contexts and check if this article has been supported or disputed.
https://scite.ai/reports/10.1016/s0304-3835(01)00654-1

Article citations

The Emerging Key Role of the mGluR1-PKCγ Signaling Pathway in the Pathogenesis of Spinocerebellar Ataxias: A Neurodevelopmental Viewpoint.

Differentiation of Monocytic Cells Is Accompanied by a Change in the Expression of the Set of Oct-1 Isoforms.

Modeling the dynamics of transcriptional gene regulatory networks for animal development.

Polyglutamine-expanded spinocerebellar ataxia-7 protein disrupts normal SAGA and SLIK histone acetyltransferase activity.

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Modification of octamer binding transcriptional factor is related to H2B histone gene repression during dimethyl sulfoxide-dependent differentiation of HL-60 cells.

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Dimethylsulfoxide, retinoic acid 12-O-tetradecanoyl-phorbol-13-acetate induce a selective decrease in the phosphorylation of P150, a surface membrane phosphoprotein of HL-60 cells resistant to adriamycin

Regulation of human histone gene expression: Kinetics of accumulation and changes in the rate of synthesis and half life of individual histone mRNAs during the HeLa cell cycle

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