Systems Genome: Coordinated Gene Activity Networks, Recurring Coordination Modules, and Genome Homeostasis in Developing Neurons

  • Siddhartha Dhiman
  • , Namya Manoj
  • , Michal Liput
  • , Amit Sangwan
  • , Justin Diehl
  • , Anna Balcerak
  • , Sneha Sudhakar
  • , Justyna Augustyniak
  • , Josep M. Jornet
  • , Yongho Bae
  • , Ewa K. Stachowiak
  • , Anirban Dutta
  • , Michal K. Stachowiak*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Simple Summary: A synchronized global genome is a flexible, homeostatic system that underwrites ontogenic development and deprograming in disease.

Abstract: As human progenitor cells differentiate into neurons, the activities of many genes change; these changes are maintained within a narrow range, referred to as genome homeostasis. This process, which alters the synchronization of the entire expressed genome, is distorted in neurodevelopmental diseases such as schizophrenia. The coordinated gene activity networks formed by altering sets of genes comprise recurring coordination modules, governed by the entropy-controlling action of nuclear FGFR1, known to be associated with DNA topology. These modules can be modeled as energy-transferring circuits, revealing that genome homeostasis is maintained by reducing oscillations (noise) in gene activity while allowing gene activity changes to be transmitted across networks; this occurs more readily in neuronal committed cells than in neural progenitors. These findings advance a model of an “entangled” global genome acting as a flexible, coordinated homeostatic system that responds to developmental signals, is governed by nuclear FGFR1, and is reprogrammed in disease.
Original languageEnglish
Article number5647
Number of pages41
JournalInternational Journal of Molecular Sciences
Volume25
Issue number11
DOIs
Publication statusPublished - 22 May 2024

Keywords

  • entropy
  • schizophrenia
  • noise and information processing
  • genome integration
  • development

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