Literature DB >> 10836146

The PAS superfamily: sensors of environmental and developmental signals.

Y Z Gu1, J B Hogenesch, C A Bradfield.   

Abstract

Over the past decade, PAS domains have been identified in dozens of signal transduction molecules and various forms have been found in animals, plants, and prokaryotes. In this review, we summarize this rapidly expanding research area by providing a detailed description of three signal transduction pathways that utilize PAS protein heterodimers to drive their transcriptional output. It is hoped that these model pathways can provide a framework for use in understanding the biology of the less well-understood members of this emerging superfamily, as well as of those to be characterized in the days to come. We use this review to develop the idea that most eukaryotic PAS proteins can be classified by functional similarities, as well as by predicted phylogenetic relationships. We focus on the alpha-class proteins, which often act as sensors of environmental signals, and the beta-class proteins, which typically act as broad-spectrum partners that target these heterodimers to their genomic targets.

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Year:  2000        PMID: 10836146     DOI: 10.1146/annurev.pharmtox.40.1.519

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  279 in total

1.  Circadian clock-specific roles for the light response protein WHITE COLLAR-2.

Authors:  M A Collett; J C Dunlap; J J Loros
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

2.  The hsp90 chaperone complex regulates intracellular localization of the dioxin receptor.

Authors:  A Kazlauskas; S Sundström; L Poellinger; I Pongratz
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

3.  Light and clock expression of the Neurospora clock gene frequency is differentially driven by but dependent on WHITE COLLAR-2.

Authors:  Michael A Collett; Norm Garceau; Jay C Dunlap; Jennifer J Loros
Journal:  Genetics       Date:  2002-01       Impact factor: 4.562

4.  Portosystemic shunting and persistent fetal vascular structures in aryl hydrocarbon receptor-deficient mice.

Authors:  G P Lahvis; S L Lindell; R S Thomas; R S McCuskey; C Murphy; E Glover; M Bentz; J Southard; C A Bradfield
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-12       Impact factor: 11.205

Review 5.  Two-component signal transduction in Enterococcus faecalis.

Authors:  Lynn Hancock; Marta Perego
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

6.  Activation of the aryl hydrocarbon receptor during pregnancy in the mouse alters mammary development through direct effects on stromal and epithelial tissues.

Authors:  Betina J Lew; Ravikumar Manickam; B Paige Lawrence
Journal:  Biol Reprod       Date:  2011-01-26       Impact factor: 4.285

7.  The transcription factor aryl hydrocarbon receptor nuclear translocator functions as an estrogen receptor beta-selective coactivator, and its recruitment to alternative pathways mediates antiestrogenic effects of dioxin.

Authors:  Joëlle Rüegg; Elin Swedenborg; David Wahlström; Aurelie Escande; Patrick Balaguer; Katarina Pettersson; Ingemar Pongratz
Journal:  Mol Endocrinol       Date:  2007-11-08

8.  Antioxidant responses and NRF2 in synergistic developmental toxicity of PAHs in zebrafish.

Authors:  Alicia R Timme-Laragy; Lindsey A Van Tiem; Elwood A Linney; Richard T Di Giulio
Journal:  Toxicol Sci       Date:  2009-02-20       Impact factor: 4.849

9.  Differential sensitivity to pro-oxidant exposure in two populations of killifish (Fundulus heteroclitus).

Authors:  Rachel C Harbeitner; Mark E Hahn; Alicia R Timme-Laragy
Journal:  Ecotoxicology       Date:  2013-01-18       Impact factor: 2.823

10.  Inhibition of pancreatic cancer Panc1 cell migration by omeprazole is dependent on aryl hydrocarbon receptor activation of JNK.

Authors:  Un-Ho Jin; Keshav Karki; Sang-Bae Kim; Stephen Safe
Journal:  Biochem Biophys Res Commun       Date:  2018-06-27       Impact factor: 3.575

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