Ing1 mediates p53 accumulation and chromatin modification in response to oncogenic stress (Q42517415)

1 November 2017

title

Ing1 mediates p53 accumulation and chromatin modification in response to oncogenic stress (English)

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1 November 2017

4

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1 November 2017

María Abad

1

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1 November 2017

Camino Menéndez

2

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1 November 2017

Annette Füchtbauer

3

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1 November 2017

Ernst-Martin Füchtbauer

5

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1 November 2017

Ignacio Palmero

6

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1 November 2017

language of work or name

English

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publication date

10 August 2007

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Journal of Biological Chemistry

1 November 2017

number of pages

8

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based on heuristic

inferred from page(s)

published in

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1 November 2017

volume

282

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1 November 2017

issue

42

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1 November 2017

page(s)

31060-31067

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Intrinsic tumour suppression

1 November 2017

cites work

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DNA damage-inducible gene p33ING2 negatively regulates cell proliferation through acetylation of p53

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Human ING1 proteins differentially regulate histone acetylation

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Role of the Sin3-histone deacetylase complex in growth regulation by the candidate tumor suppressor p33(ING1).

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ING tumor suppressor proteins are critical regulators of chromatin acetylation required for genome expression and perpetuation

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Solution structure and NMR characterization of the binding to methylated histone tails of the plant homeodomain finger of the tumour suppressor ING4

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The PHD finger of the chromatin-associated protein ING2 functions as a nuclear phosphoinositide receptor

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Growth inhibition by the tumor suppressor p33ING1 in immortalized and primary cells: involvement of two silencing domains and effect of Ras.

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ING2 regulates the onset of replicative senescence by induction of p300-dependent p53 acetylation

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The candidate tumour suppressor protein ING4 regulates brain tumour growth and angiogenesis

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Structure and regulation of the mouse ing1 gene. Three alternative transcripts encode two phd finger proteins that have opposite effects on p53 function

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Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a

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PML regulates p53 acetylation and premature senescence induced by oncogenic Ras

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Ras induces p21Cip1/Waf1 cyclin kinase inhibitor transcriptionally through Sp1-binding sites

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Murine fibroblasts lacking p21 undergo senescence and are resistant to transformation by oncogenic Ras.

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Targeted disruption of the mouse ing1 locus results in reduced body size, hypersensitivity to radiation and elevated incidence of lymphomas

21 January 2018

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Deletion of p37Ing1 in mice reveals a p53-independent role for Ing1 in the suppression of cell proliferation, apoptosis, and tumorigenesis

21 January 2018

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HP1 and the dynamics of heterochromatin maintenance

21 January 2018

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Components of a pathway maintaining histone modification and heterochromatin protein 1 binding at the pericentric heterochromatin in Mammalian cells

21 January 2018

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Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component

21 January 2018

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mSin3-associated protein, mSds3, is essential for pericentric heterochromatin formation and chromosome segregation in mammalian cells

21 January 2018

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Tethering of HP1 proteins to chromatin is relieved by phosphoacetylation of histone H3.

21 January 2018

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mSin3A corepressor regulates diverse transcriptional networks governing normal and neoplastic growth and survival

21 January 2018

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Oncogenic Ras induces p19ARF and growth arrest in mouse embryo fibroblasts lacking p21Cip1 and p27Kip1 without activating cyclin D-dependent kinases

21 January 2018

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Activation of ARF by oncogenic stress in mouse fibroblasts is independent of E2F1 and E2F2

21 January 2018

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p19ARF links the tumour suppressor p53 to Ras

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M701639200

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1 November 2017

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