Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractCharacterisation of odorants in roasted stem tea using gas chromatography-mass spectrometry and gas chromatography-olfactometry analysis    Next AbstractFloral volatiles evoke partially similar responses in both florivores and pollinators and are correlated with non-volatile reward chemicals »

Cancer Res


Title:Identification of the interleukin 4 receptor alpha gene as a direct target for p73
Author(s):Sasaki Y; Mita H; Toyota M; Ishida S; Morimoto I; Yamashita T; Tanaka T; Imai K; Nakamura Y; Tokino T;
Address:"Department of Molecular Biology, Cancer Research Institute, Sapporo Medical University School of Medicine, Sapporo, Japan"
Journal Title:Cancer Res
Year:2003
Volume:63
Issue:23
Page Number:8145 - 8152
DOI:
ISSN/ISBN:0008-5472 (Print) 0008-5472 (Linking)
Abstract:"p73 has a high degree of structural homology to p53 and can activate transcription of p53-responsive genes. However, analysis of p73-deficient mice revealed a marked divergence in the physiological activities of p53 family genes and distinguishes p73 from p53. Mice deficient for p73 exhibit profound defects, including hippocampal dysgenesis, chronic infection, and inflammation, as well as abnormalities in pheromone sensory pathways. p73 plays important roles in neurogenesis, sensory pathways, and homeostatic regulation. Here, we found that the interleukin 4 receptor alpha (IL-4Ralpha) gene is up-regulated by p73 but not significantly by p53 in several human cancer cell lines. IL-4Ralphatranscription is also activated in response to cisplatin, a DNA-damaging agent known to induce p73. By using small interference RNA designed to target p73, we demonstrated that silencing endogenous p73 abrogates the induction of the IL-4Ralpha gene after cisplatin treatment. Furthermore, we identified a p73-binding site in the first intron of the IL-4Ralpha gene that can directly interact with the p73 protein in vivo. This p73-binding site consists of eight copies of a 10-bp consensus p53-binding motif and is a functional response element that is relatively specific for p73 among the p53 family. p73beta promoted localized nucleosomal acetylation through recruitment of coactivator p300, indicating that p73 regulates transcription of IL-4Ralpha through the unique p73-binding site. We also found that p73beta-transfected tumor cells are sensitive to IL-4-mediated apoptosis. Our data suggest that IL-4Ralpha could mediate, in part, certain immune responses and p73-dependent cell death"
Keywords:"Acetylation Apoptosis/drug effects/genetics Base Sequence Binding Sites Cell Line, Tumor Cisplatin/pharmacology Consensus Sequence DNA, Neoplasm/genetics/metabolism DNA-Binding Proteins/genetics/metabolism/*physiology Gene Expression Regulation, Neoplasti;"
Notes:"MedlineSasaki, Yasushi Mita, Hiroaki Toyota, Minoru Ishida, Setsuko Morimoto, Ichiro Yamashita, Toshiharu Tanaka, Toshihiro Imai, Kohzoh Nakamura, Yusuke Tokino, Takashi eng Research Support, Non-U.S. Gov't 2003/12/18 Cancer Res. 2003 Dec 1; 63(23):8145-52"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-11-2024