HECT ubiquitin ligase Smurf1 targets the tumor suppressor ING2 for ubiquitination and degradation (Q24338460)

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Min Wu

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Guichun Xing

4

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Shan He

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Yuxin Yin

6

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Chunyan Tian

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Fuchu He

8

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Lingqiang Zhang

The new tumor suppressor genes ING: genomic structure and status in cancer

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language of work or name

English

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publication date

16 July 2010

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published in

FEBS Letters

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volume

584

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page(s)

3005-12

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issue

14

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cites work

1 reference

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The ING gene family in the regulation of cell growth and tumorigenesis

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Different HATS of the ING1 gene family

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Leucine zipper-like domain is required for tumor suppressor ING2-mediated nucleotide excision repair and apoptosis

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

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

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

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Nuclear ING2 expression is reduced in human cutaneous melanomas

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A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation

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Smad7 binds to Smurf2 to form an E3 ubiquitin ligase that targets the TGF beta receptor for degradation

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Regulation of cell polarity and protrusion formation by targeting RhoA for degradation

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Regulation of the polarity protein Par6 by TGFbeta receptors controls epithelial cell plasticity

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Targeting WW domains linker of HECT-type ubiquitin ligase Smurf1 for activation by CKIP-1

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KRAB-type zinc-finger protein Apak specifically regulates p53-dependent apoptosis.

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Histone methyltransferase protein SETD2 interacts with p53 and selectively regulates its downstream genes

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High-throughput mapping of a dynamic signaling network in mammalian cells

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Ubiquitin ligase Smurf1 targets TRAF family proteins for ubiquitination and degradation

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Regulation of planar cell polarity by Smurf ubiquitin ligases

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Smurf1 directly targets hPEM-2, a GEF for Cdc42, via a novel combination of protein interaction modules in the ubiquitin-proteasome pathway

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The Nedd4 family of E3 ubiquitin ligases: functional diversity within a common modular architecture

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Cloning of a novel gene (ING1L) homologous to ING1, a candidate tumor suppressor

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Phylogenetic analysis of the ING family of PHD finger proteins

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The tumor suppressor ING3 is degraded by SCF(Skp2)-mediated ubiquitin-proteasome system

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NAD(P)H quinone oxidoreductase 1 inhibits the proteasomal degradation of the tumour suppressor p33(ING1b)

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Two wobble-splicing events affect ING4 protein subnuclear localization and degradation

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ONCOGENESIS: Landscaping the Cancer Terrain

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Decreased expression of ING2 gene and its clinicopathological significance in hepatocellular carcinoma

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inferred from DOI database lookup

7 January 2021

based on heuristic

Molecular mechanism of histone H3K4me3 recognition by plant homeodomain of ING2

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.05.033

inferred from DOI database lookup

7 January 2021

based on heuristic

ING2 PHD domain links histone H3 lysine 4 methylation to active gene repression

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2010.05.033