نتایج جستجو برای: tat

تعداد نتایج: 6516  

Journal: :Journal of virology 1999
B A Morse L M Carruth J E Clements

The visna virus Tat protein is required for efficient viral transcription from the visna virus long terminal repeat (LTR). AP-1 sites within the visna virus LTR, which can be bound by the cellular transcription factors Fos and Jun, are also necessary for Tat-mediated transcriptional activation. A potential mechanism by which the visna virus Tat protein could target the viral promoter is by prot...

Journal: :Current Biology 1999
Melanie Ott Martina Schnölzer Jerry Garnica Wolfgang Fischle Stephane Emiliani Hans-Richard Rackwitz Eric Verdin

The human immunodeficiency virus 1 (HIV-1) Tat protein activates transcriptional elongation by recruiting the positive transcription elongation factor (pTEFb) complex to the TAR RNA element, which is located at the 5' extremity of all viral transcripts [1-3]. Tat also associates in vitro and in vivo with the transcriptional coactivator p300/CBP [4-6]. This association has been proposed to recru...

Journal: :The Journal of infectious diseases 2000
R Benelli A Barbero S Ferrini P Scapini M Cassatella F Bussolino C Tacchetti D M Noonan A Albini

The extracellular activities of the human immunodeficiency virus (HIV) transactivator protein (Tat) include induction of angiogenesis and stimulation of monocyte migration. Here it is shown that polymorphonuclear leukocytes (PMNL), mostly neutrophils, rapidly invade in response to Tat in vivo and initiate the formation of new vessels. In vitro, Tat was chemotactic for PMNL and induced calcium (...

Journal: :Molecular microbiology 2003
Stefania Meloni Luis Rey Stephan Sidler Juan Imperial Tomás Ruiz-Argüeso José M Palacios

The Tat (twin-arginine translocation) system mediates export of periplasmic proteins in folded conformation. Proteins transported via Tat contain a characteristic twin-arginine motif in their signal peptide. Genetic determinants (tatABC genes) of the Tat system from Rhizobium leguminosarum bv. viciae were cloned and characterized, and a tatBC deletion mutant was constructed. The mutant lacked t...

2008
Jing Ai Xianliang Xin Mingyue Zheng Shuai Wang Shuying Peng Jing Li Limei Wang Hualiang Jiang Meiyu Geng

Tat protein, released by HIV-infected cells, has a battery of important biological effects leading to distinct AIDS-associated pathologies. Cell surface heparan sulfate protoglycans (HSPGs) have been accepted as endogenous Tat receptors, and the Tat basic domain has been identified as the heparin binding site. However, findings that deletion or substitution of the basic domain inhibits but does...

Journal: :Journal of virology 1995
C D Southgate M R Green

Lentivirus Tat proteins comprise a novel class of RNA-binding transcriptional activators that are essential for viral replication. In this study, we performed a series of protein fusion experiments to delineate the minimal protein domains and promoter elements required for Tat action. We show that a 15-amino-acid region of equine infectious anemia virus (EIAV) Tat protein, when fused to the GAL...

Journal: :The Journal of biological chemistry 2001
M Rusnati C Urbinati A Caputo L Possati H Lortat-Jacob M Giacca D Ribatti M Presta

HIV-1 Tat protein, released from HIV-infected cells, may act as a pleiotropic heparin-binding growth factor. From this observation, extracellular Tat has been implicated in the pathogenesis of AIDS and of AIDS-associated pathologies. Here we demonstrate that the heparin analog pentosan polysulfate (PPS) inhibits the interaction of glutathione S-transferase (GST)-Tat protein with heparin immobil...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2005
Chunxiang Zhang Deepti Chaturvedi Laura Jaggar Debra Magnuson John M Lee Tarun B Patel

OBJECTIVE To determine whether the human sprouty 2 (hSPRY2) protein, an inhibitor of receptor tyrosine kinase actions, regulates vascular smooth muscle cell (VSMC) proliferation, migration, and neointima formation in injured carotid artery. METHODS AND RESULTS The hSPRY2 protein or green fluorescent protein (GFP; control) was transduced into VSMCs by placing an N-terminal TAT epitope on the p...

2004
Katsuya Hirano Dmitry N. Derkach Mayumi Hirano Junji Nishimura Shosuke Takahashi Hideo Kanaide

Objective—The region of the 110 kDa regulatory subunit (MYPT1) of smooth muscle myosin phosphatase involved in the regulation of contraction was determined under physiological conditions. Methods and Results—Using HIV Tat protein-mediated protein transduction, the N-terminal fragments of MYPT1 were introduced to the intact porcine coronary arterial strips. Pre-incubation with 3 mol/L TAT-MYPT1,...

2017
Jianru Pan Huocong He Ying Su Guangjin Zheng Junxin Wu Shutao Liu Pingfan Rao

GST-TAT-SOD was the fusion of superoxide dismutase (SOD), cell-permeable peptide TAT, and glutathione-S-transferase (GST). It was proved to be a potential selective radioprotector in vitro in our previous work. This study evaluated the in vivo radioprotective activity of GST-TAT-SOD against whole-body irradiation. We demonstrated that intraperitoneal injection of 0.5 ml GST-TAT-SOD (2 kU/ml) 2 ...

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