Fraile Beneitez, RodrigoSánchez Mir, LauraMurciano-Julià, GuillemAyté del Olmo, JoséHidalgo Hernando, Elena2022-09-142022-09-142022Fraile R, Sánchez-Mir L, Murciano-Julià G, Ayté J, Hidalgo E. A stress-blinded Atf1 can fully assemble heterochromatin in a RNAi-independent minimal mat locus but impairs directionality of mat2/3 switching. iScience. 2022 Aug 2;25(8):104820. DOI: 10.1016/j.isci.2022.1048202589-0042http://hdl.handle.net/10230/54061The MAP kinase Sty1 phosphorylates and activates the transcription factor Atf1 in response to several stress conditions, which then shifts from a transcriptional repressor to an activator. Atf1 also participates in heterochromatin assembly at the mat locus, in combination with the RNA interference (RNAi) machinery. Here, we study the role of signal-dependent phosphorylation of Atf1 in heterochromatin establishment at mat, using different Atf1 phospho mutants. Although a hypo-phosphorylation Atf1 mutant, Atf1.10M, mediates heterochromatin assembly, the phosphomimic Atf1.10D is unable to maintain silencing. In a minimal mat locus, lacking the RNAi-recruiting cis elements and displaying intermediate silencing, Atf1.10M restores full heterochromatin and silencing. However, evolution experiments with this stress-blinded Atf1.10M show that it is unable to facilitate switching between the donor site mat3 and mat1. We propose that the unphosphorylated, inactive Atf1 contributes to proper heterochromatin assembly by recruiting repressive complexes, but its stress-dependent phosphorylation is required for recombination/switching to occur.application/pdfeng© 2022 The Author(s). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).A stress-blinded Atf1 can fully assemble heterochromatin in a RNAi-independent minimal mat locus but impairs directionality of mat2/3 switchinginfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.isci.2022.104820EpigeneticsFunctional aspects of cell biologyMolecular biologyMolecular mechanism of gene regulationinfo:eu-repo/semantics/openAccess