PAS Domains: Internal Sensors of Oxygen, Redox Potential, and Light
- 1 June 1999
- journal article
- research article
- Published by American Society for Microbiology in Microbiology and Molecular Biology Reviews
- Vol. 63 (2) , 479-506
- https://doi.org/10.1128/mmbr.63.2.479-506.1999
Abstract
SUMMARY PAS domains are newly recognized signaling domains that are widely distributed in proteins from members of the Archaea and Bacteria and from fungi, plants, insects, and vertebrates. They function as input modules in proteins that sense oxygen, redox potential, light, and some other stimuli. Specificity in sensing arises, in part, from different cofactors that may be associated with the PAS fold. Transduction of redox signals may be a common mechanistic theme in many different PAS domains. PAS proteins are always located intracellularly but may monitor the external as well as the internal environment. One way in which prokaryotic PAS proteins sense the environment is by detecting changes in the electron transport system. This serves as an early warning system for any reduction in cellular energy levels. Human PAS proteins include hypoxia-inducible factors and voltage-sensitive ion channels; other PAS proteins are integral components of circadian clocks. Although PAS domains were only recently identified, the signaling functions with which they are associated have long been recognized as fundamental properties of living cells.Keywords
This publication has 271 references indexed in Scilit:
- Synergistic Kinetic Interactions between Components of the Phosphorelay Controlling Sporulation in Bacillus subtilisBiochemistry, 1998
- cDNA Cloning and Tissue-Specific Expression of a Novel Basic Helix–Loop–Helix/PAS Protein (BMAL1) and Identification of Alternatively Spliced Variants with Alternative Translation Initiation Site UsageBiochemical and Biophysical Research Communications, 1997
- Molecular Evolution of the C-terminal Cytoplasmic Domain of a Superfamily of Bacterial Receptors Involved in TaxisJournal of Molecular Biology, 1996
- Characterization ofmsim,a Murine Homologue of theDrosophila simTranscription FactorGenomics, 1996
- A gene from the photosynthetic gene cluster ofRhodobacter sphaeroides inducestrans suppression of bacteriochlorophyll and carotenoid levels inR. sphaeroides andR. capsulatusCurrent Microbiology, 1991
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Chemotransduction in the Carotid Body: K + Current Modulated by P O 2 In Type I Chemoreceptor CellsScience, 1988
- Adaptation of the bacterial photosynthetic apparatus to different light intensitiesTrends in Biochemical Sciences, 1986
- Sensing of ΔμH+ in phototaxis of Halobacterium halobiumNature, 1981
- Reception of the energy level in bacterial taxisJournal of Theoretical Biology, 1980