Source:http://linkedlifedata.com/resource/pubmed/id/17314097
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rdf:type | |
lifeskim:mentions |
umls-concept:C0031727,
umls-concept:C0039371,
umls-concept:C0079904,
umls-concept:C0086427,
umls-concept:C0205224,
umls-concept:C0271510,
umls-concept:C0332307,
umls-concept:C0599894,
umls-concept:C0851285,
umls-concept:C1521840,
umls-concept:C1552644,
umls-concept:C1704708,
umls-concept:C1705914,
umls-concept:C1709060,
umls-concept:C1823153,
umls-concept:C2349976
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pubmed:issue |
16
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pubmed:dateCreated |
2007-4-16
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pubmed:abstractText |
The switching on-and-off of I-kappaB kinase (IKK) and NF-kappaB occurs rapidly after signaling. How activated IKK becomes down-regulated is not well understood. Here we show that following tumor necrosis factor-alpha stimulation, protein phosphatase 2A (PP2A) association with IKK is increased. A heptad repeat in IKKgamma, helix 2 (HLX2), mediates PP2A recruitment. Two other heptad repeats downstream of HLX2, termed coiled-coil region 2 (CCR2) and leucine zipper (LZ), bind HLX2 and negatively regulate HLX2 interaction with PP2A. HTLV-1 transactivator Tax also binds HLX2, and this interaction is enhanced by CCR2 but reduced by LZ. In the presence of Tax, PP2A-IKKgamma binding is greatly strengthened. Interestingly, peptides spanning CCR2 and/or LZ disrupt IKKgamma-Tax and IKKgamma-PP2A interactions and potently inhibit NF-kappaB activation by Tax and tumor necrosis factor-alpha. We propose that when IKK is resting, HLX2, CCR2, and LZ form a helical bundle in which HLX2 is sequestered. The HLX2-CCR2-LZ bundle becomes unfolded by signal-induced modifications of IKKgamma or after Tax binding. In this conformation, IKK becomes activated. IKKgamma then recruits PP2A via the exposed HLX2 domain for rapid down-regulation of IKK. Tax-PP2A interaction, however, renders PP2A inactive, thus maintaining Tax-PP2A-IKK in an active state. Finally, CCR2 and LZ possibly inhibit IKK activation by stabilizing the HLX2-CCR2-LZ bundle.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Gene Products, tax,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Transferase,
http://linkedlifedata.com/resource/pubmed/chemical/I-kappa B Kinase,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoprotein Phosphatases,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Phosphatase 2
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
282
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
12119-26
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17314097-Animals,
pubmed-meshheading:17314097-Cell Line,
pubmed-meshheading:17314097-Cell Line, Tumor,
pubmed-meshheading:17314097-Gene Expression Regulation, Viral,
pubmed-meshheading:17314097-Gene Products, tax,
pubmed-meshheading:17314097-Glutathione Transferase,
pubmed-meshheading:17314097-Humans,
pubmed-meshheading:17314097-I-kappa B Kinase,
pubmed-meshheading:17314097-Mice,
pubmed-meshheading:17314097-Models, Genetic,
pubmed-meshheading:17314097-NF-kappa B,
pubmed-meshheading:17314097-Phosphoprotein Phosphatases,
pubmed-meshheading:17314097-Protein Binding,
pubmed-meshheading:17314097-Protein Phosphatase 2,
pubmed-meshheading:17314097-Protein Structure, Tertiary,
pubmed-meshheading:17314097-Two-Hybrid System Techniques
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pubmed:year |
2007
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pubmed:articleTitle |
Heptad repeats regulate protein phosphatase 2a recruitment to I-kappaB kinase gamma/NF-kappaB essential modulator and are targeted by human T-lymphotropic virus type 1 tax.
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pubmed:affiliation |
Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
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