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Journal of Biological Chemistry
Article . 2002 . Peer-reviewed
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Journal of Biological Chemistry
Article
License: CC BY
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Induction of Homologue of Slimb Ubiquitin Ligase Receptor by Mitogen Signaling

Authors: Vladimir S, Spiegelman; Weigang, Tang; Andrew M, Chan; Makoto, Igarashi; Stuart A, Aaronson; David A, Sassoon; Masaru, Katoh; +2 Authors

Induction of Homologue of Slimb Ubiquitin Ligase Receptor by Mitogen Signaling

Abstract

Homologue of Slimb (HOS) is the substrate-recognizing component of the SCF(HOS)-Roc1 E3 ubiquitin protein ligase. This ligase mediates ubiquitination of the inhibitor of NF-kappaB transcription factor (IkappaB). We have found that HOS is highly expressed in a number of human cancer cell lines. The rates of the HOS gene transcription as well as HOS mRNA and protein levels were up-regulated in cells treated with mitogens or transfected with the inducers of mitogen-activated protein kinase pathway. Conversely, mitogen withdrawal strikingly reduced HOS levels during differentiation of mouse myoblasts. Activators of mitogen-activated protein kinase accelerated IkappaBalpha degradation and increased NF-kappaB transcriptional activity. Inhibition of HOS function via expression of dominant negative HOS (HOS(DeltaF)) initiated mouse myoblast differentiation and prevented Ras-mediated acceleration of IkappaBalpha degradation as well as NF-kappaB trans-activation and transformation of NIH3T3 cells. These data link the induction of HOS in proliferating cells with mitogen-signaling-dependent inhibition of cell differentiation and promotion of cell transformation.

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Keywords

Cell Nucleus, Dose-Response Relationship, Drug, Immunoblotting, NF-kappa B, Down-Regulation, Cell Differentiation, 3T3 Cells, Fibroblasts, Blotting, Northern, Ornithine Decarboxylase, Precipitin Tests, Enzyme Activation, Ligases, Mice, Cell Transformation, Neoplastic, Animals, Humans, Mitogens, Genes, Dominant, Signal Transduction

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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    58
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
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    Top 10%
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    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
58
Top 10%
Top 10%
Top 10%
gold
Related to Research communities
Cancer Research