4.5 Article

Epigenetic cell fate inCandida albicansis controlled by transcription factor condensates acting at super-enhancer-like elements

Journal

NATURE MICROBIOLOGY
Volume 5, Issue 11, Pages 1374-+

Publisher

NATURE RESEARCH
DOI: 10.1038/s41564-020-0760-7

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Funding

  1. National Institute of Allergy and Infectious Disease [AI081704, AI135228, AI141893, AI137975]
  2. Burroughs Wellcome Fund (PATH award)
  3. National Heart, Lung and Blood Institute [T32HL134625]
  4. National Institute of Dental and Craniofacial Research [F31DE02968001]
  5. National Institute of Mental Health [T32MH020068]
  6. National Institute of Neurological Disorders and Stroke [F31NS110301]
  7. Howard Hughes Medical Institute International Student Fellowship
  8. National Institute of General Medical Sciences [GM120554, GM118530]
  9. Welch Foundation [F-1808]
  10. National Science Foundation [1453358, 1845734]
  11. Div Of Molecular and Cellular Bioscience
  12. Direct For Biological Sciences [1845734] Funding Source: National Science Foundation
  13. Div Of Molecular and Cellular Bioscience
  14. Direct For Biological Sciences [1453358] Funding Source: National Science Foundation

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This study reveals that prion-like domains support the assembly of transcription factor complexes that control fungal cell identity and highlights parallels with the 'super-enhancers' that regulate mammalian cell fate. Cell identity in eukaryotes is controlled by transcriptional regulatory networks that define cell-type-specific gene expression. In the opportunistic fungal pathogenCandida albicans, transcriptional regulatory networks regulate epigenetic switching between two alternative cell states, 'white' and 'opaque', that exhibit distinct host interactions. In the present study, we reveal that the transcription factors (TFs) regulating cell identity contain prion-like domains (PrLDs) that enable liquid-liquid demixing and the formation of phase-separated condensates. Multiple white-opaque TFs can co-assemble into complex condensates as observed on single DNA molecules. Moreover, heterotypic interactions between PrLDs support the assembly of multifactorial condensates at a synthetic locus within live eukaryotic cells. Mutation of the Wor1 TF revealed that substitution of acidic residues in the PrLD blocked its ability to phase separate and co-recruit other TFs in live cells, as well as its function inC. albicanscell fate determination. Together, these studies reveal that PrLDs support the assembly of TF complexes that control fungal cell identity and highlight parallels with the 'super-enhancers' that regulate mammalian cell fate.

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