1. Atf1-Pcr1-M26 complex links stress-activated MAPK and cAMP-dependent protein kinase pathways via chromatin remodeling of cgs2+.
- Author
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Davidson MK, Shandilya HK, Hirota K, Ohta K, and Wahls WP
- Subjects
- 3',5'-Cyclic-AMP Phosphodiesterases genetics, Activating Transcription Factor 1, Binding Sites, Cell Separation, Chromatin metabolism, Cyclic AMP metabolism, Cyclic AMP-Dependent Protein Kinases chemistry, DNA chemistry, Dimerization, Flow Cytometry, Genotype, Models, Genetic, Mutation, Nitrogen chemistry, Phosphoproteins metabolism, Promoter Regions, Genetic, Protein Binding, Reverse Transcriptase Polymerase Chain Reaction, Schizosaccharomyces pombe Proteins genetics, Schizosaccharomyces pombe Proteins metabolism, Signal Transduction, Transcriptional Activation, 3',5'-Cyclic-AMP Phosphodiesterases chemistry, Chromatin chemistry, Cyclic AMP-Dependent Protein Kinases metabolism, Gene Expression Regulation, Fungal, MAP Kinase Signaling System, Phosphoproteins physiology, Schizosaccharomyces enzymology, Schizosaccharomyces pombe Proteins chemistry, Schizosaccharomyces pombe Proteins physiology
- Abstract
Although co-ordinate interaction between different signal transduction pathways is essential for developmental decisions, interpathway connections are often obscured and difficult to identify due to cross-talk. Here signals from the fission yeast stress-activated MAPK Spc1 are shown to regulate Cgs2, a negative regulator of the cAMP-dependent protein kinase (protein kinase A) pathway. Pathway integration is achieved via Spc1-dependent binding of Atf1-Pcr1 heterodimer to an M26 DNA site in the cgs2+ promoter, which remodels chromatin to regulate expression of cgs2+ and targets downstream of protein kinase A. This direct interpathway connection co-ordinates signals of nitrogen and carbon source depletion to affect a G0 cell-cycle checkpoint and sexual differentiation. The Atf1-Pcr1-M26 complex-dependent chromatin remodeling provides a molecular mechanism whereby Atf1-Pcr1 heterodimer can function differentially as either a transcriptional activator, or as a transcriptional repressor, or as an inducer of meiotic recombination. We also show that the Atf1-Pcr1-M26 complex functions as both an inducer and repressor of chromatin remodeling, which provides a way for various chromatin remodeling-dependent effector functions to be regulated.
- Published
- 2004
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