Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
ARE- and TRE-mediated regulation of gene expression. Response to xenobiotics and antioxidants.
T Xie; M Belinsky; Y Xu; A K Jaiswal (Profiled Author: Anil K Jaiswal)
Department of Pharmacology, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
The Journal of biological chemistry 1995;270(12):6894-900.
Antioxidant response elements (AREs) containing 12-O-tetradecanoylphorbol-13-acetate response element (TRE) (perfect AP1) and TRE-like (imperfect AP1) elements mediate high basal transcription of the NAD(P)H:quinone oxidoreductase1 (NQO1) and glutathione S-transferase Ya genes in tumor cells and its induction in response to xenobiotics and antioxidants. Mutations in the human NQO1 gene ARE (hARE) revealed the requirement for two TRE or TRE-like elements arranged in inverse orientation at the interval of three base pairs and a GC box for optimal expression and beta-naphthoflavone induction of the NQO1 gene. A single TRE element from the human collagenase gene failed to respond to beta-naphthoflavone. These results demonstrate that ARE (2 x TRE or TRE-like elements)-containing detoxifying enzyme genes and not genes that contain 1 x TRE are responsive to xenobiotics and antioxidants. Bandshift assays showed shifting of a complex of more or less similar mobility with hARE and TRE that could be competed by each other. Mutations in the 3'-TRE of the NQO1 gene hARE eliminated binding of nuclear proteins to the hARE and resulted in the loss of basal and induced expression, indicating that 3'-TRE is the most important element within the hARE. 5'-TRE-like element within the NQO1 gene hARE is required for xenobiotic response but may not bind to the nuclear proteins by itself. The GC box located immediately following the 3'-TRE is required for optimal expression and induction of the NQO1 gene. The comparison of AREs from several different genes indicated the requirement for specific arrangement and spacing of two TRE and TRE-like elements within the AREs.
2 Originating Grant
-
1.
JAISWAL, ANIL KUMAR
Regulation of NAD(P)H:Quinone Oxidoreductases
1 July 1991 - 31 May 2015
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
-
2.
JAISWAL, ANIL K
REGULATION OF NAD(P)H--QUINONE OXIDOREDUCTASES
1 July 1991 - 30 November 1996
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Publications
-
1.
1992Y Li; A K Jaiswal
The Journal of biological chemistry 1992;267(21):15097-104. -
2.
1994Y Li; A K Jaiswal
European journal of biochemistry / FEBS 1994;226(1):31-9. -
3.
1998R Venugopal; A K Jaiswal
Oncogene 1998;17(24):3145-56.
Related Topics
Appears in this Publication
-
Antioxidant Response Element...
-
NAD(P)H Dehydrogenase (Quino...
-
-
-
-
-
-
Chloramphenicol O-Acetyltran...
-
-
-
-
-
-
-
-
-
Gene Expression Regulation, ...
-
-
-
Related Experts
Author of this Publication
-
Internal ExpertsPublications
-
135









-
19









-
172









-
195









-
67









-
29









