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HMBA releases P-TEFb from HEXIM1 and 7SK snRNA via PI3K/Akt and activities HIV transcription
Contreras, Xavier (Avtor), Barborič, Matjaž (Avtor), Lenasi, Tina (Avtor), Peterlin, Matija Boris (Avtor)

URLURL - Predstavitvena datoteka, za dostop obiščite http://pathogens.plosjournals.org/perlserv/?request=get-document&doi=10.1371%2Fjournal.ppat.0030146 Povezava se odpre v novem oknu

Izvleček
Hexamethylene bisacetamide (HMBA) is a potent inducer of cell differentiation and HIV production in chronically infected cells. However, its mechanism of action remains poorly defined. In this study, we demonstrate that HMBA activates transiently the PI3K/Act pathway, which leads to the phosphorylation of HEXIM1 and the subsequent release of active positive transcription elongation factor b (P-TEFb) from its transcriptionally inactivecomplex with HEXIM1 and 7SK small nuclear RNA (snRNA). As a result, P-TEFb is recruited tothe HIV promotoer to stimulate transcription elongation and viral production. Despite the continuous presence of HMBA, the released P-TEFb reassembles rapidly with 7SK sn RNA and HEXIM1. In contrast, a mutant HEXIM1 protein that cannot be phosphorrylated and released from P-TEFb and 7SK snRNA via the PI3K/Act pathway antagonizes this HMBA-mediated induction of viral production. Thus, our studies reveal how transcription is induced by HMBA and suggest how modifications in the equilibrium between active and inactive P-TEFb could contribute to cell differentiation.

Jezik:Angleški jezik
Ključne besede:infekcijske bolezni, AIDS, HIV, molekularna genetika
Vrsta gradiva:Delo ni kategorizirano (r6)
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:BF - Biotehniška fakulteta
Leto izida:2007
Št. strani:str. 1459-1469
Številčenje:Letn. 3, št. 10
UDK:575
ISSN pri članku:1553-7366
COBISS.SI-ID:2204808 Povezava se odpre v novem oknu
Število ogledov:516
Število prenosov:143
Metapodatki:XML RDF-CHPDL DC-XML DC-RDF
 
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Naslov:PLOS pathogens
Založnik:Public Library of Science
ISSN:1553-7366
COBISS.SI-ID:513029401 Povezava se odpre v novem oknu

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