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YAP charge patterning mediates signal integration through transcriptional co-condensates.
Meyer, Kirstin; Yserentant, Klaus; Cheloor-Kovilakam, Rasmi; Ruff, Kiersten M; Chung, Chan-I; Shu, Xiaokun; Huang, Bo; Weiner, Orion D.
Affiliation
  • Meyer K; Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Yserentant K; Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Cheloor-Kovilakam R; Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Ruff KM; Department of Pharmaceutical Chemistry, UCSF, San Francisco, 94143, CA, USA.
  • Chung CI; Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Shu X; Department of Pharmaceutical Chemistry, UCSF, San Francisco, 94143, CA, USA.
  • Huang B; Department of Biomedical Engineering and Center for Biomolecular Condensates, James McKelvey School of Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
  • Weiner OD; Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
bioRxiv ; 2024 Aug 10.
Article in En | MEDLINE | ID: mdl-39149273
ABSTRACT
Transcription factor dynamics are used to selectively engage gene regulatory programs. Biomolecular condensates have emerged as an attractive signaling substrate in this process, but the underlying mechanisms are not well-understood. Here, we probed the molecular basis of YAP signal integration through transcriptional condensates. Leveraging light-sheet single-molecule imaging and synthetic condensates, we demonstrate charge-mediated co-condensation of the transcriptional regulators YAP and Mediator into transcriptionally active condensates in stem cells. IDR sequence analysis and YAP protein engineering demonstrate that instead of the net charge, YAP signaling specificity is established through its negative charge patterning that interacts with Mediator's positive charge blocks. The mutual enhancement of YAP/Mediator co-condensation is counteracted by negative feedback from transcription, driving an adaptive transcriptional response that is well-suited for decoding dynamic inputs. Our work reveals a molecular framework for YAP condensate formation and sheds new light on the function of YAP condensates for emergent gene regulatory behavior.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article