(Q33977927)

30 July 2017

title

The SANT domain of human MI-ER1 interacts with Sp1 to interfere with GC box recognition and repress transcription from its own promoter (English)

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30 July 2017

Zhihu Ding

1

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30 July 2017

Laura L Gillespie

series ordinal

2

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30 July 2017

F Corinne Mercer

series ordinal

3

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30 July 2017

Gary D Paterno

series ordinal

4

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30 July 2017

language of work or name

English

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publication date

26 April 2004

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Journal of Biological Chemistry

30 July 2017

published in

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30 July 2017

volume

279

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30 July 2017

issue

27

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30 July 2017

page(s)

28009-28016

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cDNA cloning of a novel, developmentally regulated immediate early gene activated by fibroblast growth factor and encoding a nuclear protein

30 July 2017

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1 reference

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Human MI-ER1 alpha and beta function as transcriptional repressors by recruitment of histone deacetylase 1 to their conserved ELM2 domain

21 January 2018

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Molecular cloning of human er1 cDNA and its differential expression in breast tumours and tumour-derived cell lines

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Genomic organization of the human mi-er1 gene and characterization of alternatively spliced isoforms: regulated use of a facultative intron determines subcellular localization

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Nuclear localization signals in the Xenopus FGF embryonic early response 1 protein

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The SANT domain: a putative DNA-binding domain in the SWI-SNF and ADA complexes, the transcriptional co-repressor N-CoR and TFIIIB.

21 January 2018

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The SMRT and N-CoR corepressors are activating cofactors for histone deacetylase 3

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CoREST is an integral component of the CoREST- human histone deacetylase complex

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The SANT domain of Ada2 is required for normal acetylation of histones by the yeast SAGA complex

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A SANT motif in the SMRT corepressor interprets the histone code and promotes histone deacetylation

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The GLI gene encodes a nuclear protein which binds specific sequences in the human genome

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MTA3, a Mi-2/NuRD complex subunit, regulates an invasive growth pathway in breast cancer

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Drosophila TFIID binds to a conserved downstream basal promoter element that is present in many TATA-box-deficient promoters

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A tale of three fingers: the family of mammalian Sp/XKLF transcription factors

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21 January 2018

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21 January 2018

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21 January 2018

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The Sp1-like protein BTEB3 inhibits transcription via the basic transcription element box by interacting with mSin3A and HDAC-1 co-repressors and competing with Sp1.

21 January 2018

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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

21 January 2018

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Interaction of Sp1 with the growth- and cell cycle-regulated transcription factor E2F

21 January 2018

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Evidence for physical interaction between the zinc-finger transcription factors YY1 and Sp1

21 January 2018

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Cell cycle-regulated association of E2F1 and Sp1 is related to their functional interaction

21 January 2018

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Association of p107 with Sp1: genetically separable regions of p107 are involved in regulation of E2F- and Sp1-dependent transcription

21 January 2018

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The promyelocytic leukemia protein interacts with Sp1 and inhibits its transactivation of the epidermal growth factor receptor promoter

21 January 2018

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POZ domain transcription factor, FBI-1, represses transcription of ADH5/FDH by interacting with the zinc finger and interfering with DNA binding activity of Sp1

21 January 2018

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21 January 2018

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pRB induces Sp1 activity by relieving inhibition mediated by MDM2.

21 January 2018

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Histone deacetylase 1 can repress transcription by binding to Sp1.

21 January 2018

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RBP1 recruits both histone deacetylase-dependent and -independent repression activities to retinoblastoma family proteins

21 January 2018

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Stra13 expression is associated with growth arrest and represses transcription through histone deacetylase (HDAC)-dependent and HDAC-independent mechanisms

21 January 2018

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Ligand-dependent nuclear receptor corepressor LCoR functions by histone deacetylase-dependent and -independent mechanisms

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M403793200

1 reference

30 July 2017

1 reference