Identification of CCAAT displacement protein (CDP/cut) as a locus-specific repressor of major histocompatibility complex gene expression in human tumor cells (Q44878113)

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scientific article published on 17 November 2000

Language	Label	Description	Also known as
English	Identification of CCAAT displacement protein (CDP/cut) as a locus-specific repressor of major histocompatibility complex gene expression in human tumor cells	scientific article published on 17 November 2000

Statements

scholarly article

1 reference

Europe PubMed Central

7 December 2017

Identification of CCAAT displacement protein (CDP/cut) as a locus-specific repressor of major histocompatibility complex gene expression in human tumor cells (English)

1 reference

Europe PubMed Central

7 December 2017

author name string

Snyder SR

1

1 reference

Europe PubMed Central

7 December 2017

Wang J

2

1 reference

Europe PubMed Central

7 December 2017

Waring JF

3

1 reference

Europe PubMed Central

7 December 2017

Ginder GD

4

1 reference

Europe PubMed Central

7 December 2017

language of work or name

0 references

publication date

17 November 2000

1 reference

Europe PubMed Central

7 December 2017

Journal of Biological Chemistry

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Europe PubMed Central

7 December 2017

276

1 reference

Europe PubMed Central

7 December 2017

7

1 reference

Europe PubMed Central

7 December 2017

5323-5330

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Europe PubMed Central

7 December 2017

Human cytotoxic T-lymphocyte recognition of an HLA-A3 gene product expressed on murine L cells: the only human gene product required on the target cells for lysis is the class I heavy chain

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HLA-E is a major ligand for the natural killer inhibitory receptor CD94/NKG2A

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In vivo expression of natural killer cell inhibitory receptors by human melanoma-specific cytolytic T lymphocytes

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Molecular mechanisms used by tumors to escape immune recognition: immunogenetherapy and the cell biology of major histocompatibility complex class I.

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Markedly decreased expression of class I histocompatibility antigens, protein, and mRNA in human small-cell lung cancer

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A transcription factor interacting with the class I gene enhancer is inactive in tumorigenic cell lines which suppress major histocompatibility complex class I genes

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Regulation of MHC class I and II gene transcription: differences and similarities

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Adenovirus 12-mediated down-regulation of the major histocompatibility complex (MHC) class I promoter: identification of a negative regulatory element responsive to Ad12 E1A

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Transcriptional regulation of MHC class I gene expression in rat oligodendrocytes.

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Negative regulation of the major histocompatibility complex class I promoter in embryonal carcinoma cells

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Negative regulation of the major histocompatibility class I gene in undifferentiated embryonal carcinoma cells

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In vivo function of regulatory DNA sequence elements of a major histocompatibility complex class I gene

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Regulation of major histocompatibility complex class I gene expression in thyroid cells. Role of the cAMP response element-like sequence

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A complex regulatory DNA element associated with a major histocompatibility complex class I gene consists of both a silencer and an enhancer

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MHC class I heavy chain mRNA must exceed a threshold level for the reconstitution of cell surface expression of class I MHC complexes in cells transformed by the highly oncogenic adenovirus 12.

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Natural variation of the expression of HLA and endogenous antigen modulates CTL recognition in an in vitro melanoma model

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Molecular organization of the class I genes of human major histocompatibility complex

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Site-directed mutagenesis by overlap extension using the polymerase chain reaction

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Interferon-gamma induction of the human leukocyte antigen-E gene is mediated through binding of a complex containing STAT1alpha to a distinct interferon-gamma-responsive element

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Human CCAAT displacement protein is homologous to the Drosophila homeoprotein, cut

1 reference

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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

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Methylation of the minimal promoter of an embryonic globin gene silences transcription in primary erythroid cells

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MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex

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Sequence-specific DNA binding of individual cut repeats of the human CCAAT displacement/cut homeodomain protein

1 reference

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CCAAT displacement activity involves CUT repeats 1 and 2, not the CUT homeodomain

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The molecular biology of the CCAAT-binding factor NF-Y

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Primary structure and expression of a product from cut, a locus involved in specifying sensory organ identity in Drosophila

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The nuclear matrix protein CDP represses hepatic transcription of the human cholesterol-7alpha hydroxylase gene.

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Human cut-like repressor protein binds TGFbeta type II receptor gene promoter

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Repressor activity of CCAAT displacement protein in HL-60 myeloid leukemia cells.

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The human cut homeodomain protein represses transcription from the c-myc promoter

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The mammalian Cut homeodomain protein functions as a cell-cycle-dependent transcriptional repressor which downmodulates p21WAF1/CIP1/SDI1 in S phase

1 reference

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Repressor elements in the coding region of the human histone H4 gene interact with the transcription factor CDP/cut

1 reference

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CCAAT displacement protein (CDP/cut) binds a negative regulatory element in the human tryptophan hydroxylase gene

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CDP is a repressor of mouse mammary tumor virus expression in the mammary gland

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Cux/CDP homeoprotein is a component of NF-muNR and represses the immunoglobulin heavy chain intronic enhancer by antagonizing the bright transcription activator

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DNA-binding specificity of the cut repeats from the human cut-like protein

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TRANSFAC: an integrated system for gene expression regulation

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The human cut homeodomain protein can repress gene expression by two distinct mechanisms: active repression and competition for binding site occupancy

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Two upstream elements activate transcription of a major histocompatibility complex class I genein vitro

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Mutually exclusive interaction of the CCAAT-binding factor and of a displacement protein with overlapping sequences of a histone gene promoter

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The protein CDP, but not CP1, footprints on the CCAAT region of the γ-globin gene in unfractionated B-cell extracts

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Major histocompatibility antigens: the human (HLA-A, -B, -C) and murine (H-2K, H-2D) class I molecules

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Defective expression of MHC class I antigens is frequent in B-cell lymphomas of high-grade malignancy

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The human leukocyte antigen A2 interferon-stimulated response element consensus sequence binds a nuclear factor required for constitutive expression

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A multiplicity of CCAAT box-binding proteins

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Transcriptional repression of the cystic fibrosis transmembrane conductance regulator gene, mediated by CCAAT displacement protein/cut homolog, is associated with histone deacetylation

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Identifiers

10.1074/JBC.M009454200

1 reference

Europe PubMed Central

7 December 2017

1 reference

Europe PubMed Central

7 December 2017

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