Tumor suppressor NM23-H1 is a granzyme A-activated DNase during CTL-mediated apoptosis, and the nucleosome assembly protein SET is its inhibitor (Q28182042)

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scientific article (publication date: 7 March 2003)

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English	Tumor suppressor NM23-H1 is a granzyme A-activated DNase during CTL-mediated apoptosis, and the nucleosome assembly protein SET is its inhibitor	scientific article (publication date: 7 March 2003)

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scholarly article

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Tumor suppressor NM23-H1 is a granzyme A-activated DNase during CTL-mediated apoptosis, and the nucleosome assembly protein SET is its inhibitor (English)

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apoptotic process

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author name string

Zusen Fan

1

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Paul J Beresford

2

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David Y Oh

3

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Dong Zhang

4

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Judy Lieberman

5

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language of work or name

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publication date

7 March 2003

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112

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5

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659-72

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Tumor suppression and potentiation by manipulation of pp32 expression

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Recombinant human granzyme A binds to two putative HLA-associated proteins and cleaves one of them

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Granzyme A loading induces rapid cytolysis and a novel form of DNA damage independently of caspase activation

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Granzyme A activates an endoplasmic reticulum-associated caspase-independent nuclease to induce single-stranded DNA nicks

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DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall.

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Protein ligands to HuR modulate its interaction with target mRNAs in vivo

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The oncoprotein Set/TAF-1beta, an inhibitor of histone acetyltransferase, inhibits active demethylation of DNA, integrating DNA methylation and transcriptional silencing

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Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

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A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD

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HMG2 interacts with the nucleosome assembly protein SET and is a target of the cytotoxic T-lymphocyte protease granzyme A

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Cleaving the oxidative repair protein Ape1 enhances cell death mediated by granzyme A

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Ref-1 regulates the transactivation and pro-apoptotic functions of p53 in vivo.

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DNA damage in the nucleosome core is refractory to repair by human excision nuclease

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Cloning and functional analysis of the ndk1 gene encoding nucleoside-diphosphate kinase in Schizosaccharomyces pombe

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BCL-2 blocks perforin-induced nuclear translocation of granzymes concomitant with protection against the nuclear events of apoptosis

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Multi-step chromatin degradation in apoptosis. DNA breakdown in apoptosis

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Overexpression of Helicard, a CARD-containing helicase cleaved during apoptosis, accelerates DNA degradation

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Preferential sites of early DNA cleavage in apoptosis and the pathway of nuclear damage

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The human Nm23/nucleoside diphosphate kinases

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Large-scale fragmentation of mammalian DNA in the course of apoptosis proceeds via excision of chromosomal DNA loops and their oligomers

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Endonuclease G is an apoptotic DNase when released from mitochondria

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Molecular identification of I1PP2A, a novel potent heat-stable inhibitor protein of protein phosphatase 2A.

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DFF, a heterodimeric protein that functions downstream of caspase-3 to trigger DNA fragmentation during apoptosis

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The gene for nucleoside diphosphate kinase functions as a mutator gene in Escherichia coli.

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NM23-H1 and NM23-H2 repress transcriptional activities of nuclease-hypersensitive elements in the platelet-derived growth factor-A promoter

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BRCA1: exploring the links to transcription

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Cellular localization and expression of template-activating factor I in different cell types.

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Synergistic roles of granzymes A and B in mediating target cell death by rat basophilic leukemia mast cell tumors also expressing cytolysin/perforin

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Cleavage of DNA by human NM23-H2/nucleoside diphosphate kinase involves formation of a covalent protein-DNA complex

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Human c-myc transcription factor PuF identified as nm23-H2 nucleoside diphosphate kinase, a candidate suppressor of tumor metastasis

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Mutational analysis of NM23-H2/NDP kinase identifies the structural domains critical to recognition of a c-myc regulatory element

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Catalysis of DNA cleavage and nucleoside triphosphate synthesis by NM23-H2/NDP kinase share an active site that implies a DNA repair function

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Structure-based mutational and functional analysis identify human NM23-H2 as a multifunctional enzyme

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Lymphocyte-mediated cytotoxicity.

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Target cell lysis by CTL granule exocytosis is independent of ICE/Ced-3 family proteases

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Regulation of histone acetylation and transcription by INHAT, a human cellular complex containing the set oncoprotein

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Regulation of histone acetylation and transcription by nuclear protein pp32, a subunit of the INHAT complex.

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Direct cleavage of the human DNA fragmentation factor-45 by granzyme B induces caspase-activated DNase release and DNA fragmentation

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A natural killer cell granule protein that induces DNA fragmentation and apoptosis

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Functional interaction between nucleosome assembly proteins and p300/CREB-binding protein family coactivators

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Granzyme A initiates an alternative pathway for granule-mediated apoptosis.

1 reference

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Evidence for a novel gene associated with low tumor metastatic potential

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An 'environment to nucleus' signaling system operates in B lymphocytes: redox status modulates BSAP/Pax-5 activation through Ref-1 nuclear translocation

1 reference

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DFF45/ICAD can be directly processed by granzyme B during the induction of apoptosis

1 reference

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Identification of the nuclear factor HMG2 as an activator for DFF nuclease activity

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Role of proteolysis in apoptosis: involvement of serine proteases in internucleosomal DNA fragmentation in immature thymocytes

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Granzymes A and B directly cleave lamins and disrupt the nuclear lamina during granule-mediated cytolysis

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Induction of rapid histone degradation by the cytotoxic T lymphocyte protease Granzyme A.

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Identifiers

10.1016/S0092-8674(03)00150-8

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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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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