Your browser doesn't support javascript.
loading
An activity-specificity trade-off encoded in human transcription factors.
Naderi, Julian; Magalhaes, Alexandre P; Kibar, Gözde; Stik, Gregoire; Zhang, Yaotian; Mackowiak, Sebastian D; Wieler, Hannah M; Rossi, Francesca; Buschow, Rene; Christou-Kent, Marie; Alcoverro-Bertran, Marc; Graf, Thomas; Vingron, Martin; Hnisz, Denes.
Afiliación
  • Naderi J; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Magalhaes AP; Institute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
  • Kibar G; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Stik G; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Zhang Y; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Mackowiak SD; Josep Carreras Leukaemia Research Institute, Badalona, Spain.
  • Wieler HM; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Rossi F; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Buschow R; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Christou-Kent M; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Alcoverro-Bertran M; Microscopy Core Facility, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Graf T; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Vingron M; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Hnisz D; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
Nat Cell Biol ; 26(8): 1309-1321, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38969762
ABSTRACT
Transcription factors (TFs) control specificity and activity of gene transcription, but whether a relationship between these two features exists is unclear. Here we provide evidence for an evolutionary trade-off between the activity and specificity in human TFs encoded as submaximal dispersion of aromatic residues in their intrinsically disordered protein regions. We identified approximately 500 human TFs that encode short periodic blocks of aromatic residues in their intrinsically disordered regions, resembling imperfect prion-like sequences. Mutation of periodic aromatic residues reduced transcriptional activity, whereas increasing the aromatic dispersion of multiple human TFs enhanced transcriptional activity and reprogramming efficiency, promoted liquid-liquid phase separation in vitro and more promiscuous DNA binding in cells. Together with recent work on enhancer elements, these results suggest an important evolutionary role of suboptimal features in transcriptional control. We propose that rational engineering of amino acid features that alter phase separation may be a strategy to optimize TF-dependent processes, including cellular reprogramming.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción Límite: Humans Idioma: En Revista: Nat Cell Biol Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción Límite: Humans Idioma: En Revista: Nat Cell Biol Año: 2024 Tipo del documento: Article País de afiliación: Alemania