(Q28216580)

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Sp1 and Sp3 recruit histone deacetylase to repress transcription of human telomerase reverse transcriptase (hTERT) promoter in normal human somatic cells

scientific article (publication date: 11 October 2002)

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Sp1 and Sp3 recruit histone deacetylase to repress transcription of human telomerase reverse transcriptase (hTERT) promoter in normal human somatic cells (English)

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author name string

Jaejoon Won

1

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Jeongbin Yim

2

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Tae Kook Kim

3

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language of work or name

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publication date

11 October 2002

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Journal of Biological Chemistry

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277

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41

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38230-8

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Telomere shortening and apoptosis in telomerase-inhibited human tumor cells

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The RNA component of human telomerase

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In vivo and in vitro analyses of Myc for differential promoter activities of the human telomerase (hTERT) gene in normal and tumor cells.

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Direct activation of TERT transcription by c-MYC.

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Telomerase activity in hybrids between telomerase-negative and telomerase-positive immortal human cells is repressed in the different complementation groups but not in the same complementation group of immortality

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Can ends justify the means?: telomeres and the mechanisms of replicative senescence and immortalization in mammalian cells

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Identification and characterization of negative regulatory elements of the human telomerase catalytic subunit (hTERT) gene promoter: possible role of MZF-2 in transcriptional repression of hTERT.

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Identification of Mad as a repressor of the human telomerase (hTERT) gene

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Histone deacetylation is involved in the transcriptional repression of hTERT in normal human cells

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Telomerase activation by histone deacetylase inhibitor in normal cells

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Histone deacetylase 1 can repress transcription by binding to Sp1.

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Sp3 and Sp4 can repress transcription by competing with Sp1 for the core cis-elements on the human ADH5/FDH minimal promoter

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Sp1 cooperates with c-Myc to activate transcription of the human telomerase reverse transcriptase gene (hTERT).

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Insulin-like growth factor-I regulates transcription of the elastin gene through a putative retinoblastoma control element. A role for Sp3 acting as a repressor of elastin gene transcription.

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Sp3 represses transcription when tethered to promoter DNA or targeted to promoter proximal RNA.

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Sp3 is a bifunctional transcription regulator with modular independent activation and repression domains.

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Sp1 activates and inhibits transcription from separate elements in the proximal promoter of the human adenine nucleotide translocase 2 (ANT2) gene.

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A role for Sp and helix-loop-helix transcription factors in the regulation of the human Id4 gene promoter activity

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An Sp1-binding Silencer Element Is a Critical Negative Regulator of the Megakaryocyte-specific αIIb Gene

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Activation of the p21WAF1/CIP1 promoter independent of p53 by the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) through the Sp1 sites

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Different activation domains of Sp1 govern formation of multimers and mediate transcriptional synergism

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Analysis of Sp1 in vivo reveals multiple transcriptional domains, including a novel glutamine-rich activation motif

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Telomere end-replication problem and cell aging

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Toward identifying a cellular determinant of telomerase repression

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The Wilms' tumor 1 tumor suppressor gene represses transcription of the human telomerase reverse transcriptase gene

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Identifiers

10.1074/JBC.M206064200

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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