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Positional information and information flows in dynamic tissues.

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Summary
This summary is machine-generated.

This study introduces a new framework to quantify positional information (PI) in dynamic embryonic tissues. It reveals how cell movements influence pattern formation during development, offering insights into developmental processes.

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Area of Science:

  • Developmental Biology
  • Systems Biology
  • Information Theory

Background:

  • Embryonic development involves complex processes of information storage, transmission, and transformation to generate spatial patterns.
  • Positional information (PI) is crucial for understanding pattern formation, but its quantification has been limited to static tissues due to cell motion.

Purpose of the Study:

  • To develop a novel framework for quantifying PI in dynamic embryonic tissues.
  • To decompose mutual information into information flows representing PI preservation, loss, and generation.
  • To analyze information-theoretic signatures of developmental processes like cell sorting and mixing.

Main Methods:

  • Decomposition of mutual information between cell positions and properties over time into information flows.
  • Application of the framework to whole-embryo cell trajectory data from *Drosophila*, mouse, and zebrafish gastrulation.
  • Analysis of tissue flows as dynamical systems to understand pattern formation mechanisms.

Main Results:

  • The framework reveals information-theoretic signatures of developmental processes directly from data.
  • Quantification of cell mixing and derivation of bounds on PI preservation in dynamic tissues.
  • Demonstration that morphogenesis structures cell mixing, preferentially preserving specific patterns.

Conclusions:

  • The developed framework enables information-theoretic quantification of PI in dynamic tissues, overcoming limitations of previous methods.
  • The study provides insights into how tissue dynamics and morphogenesis influence pattern formation.
  • The framework offers tools for tracing generated PI to its sources and distinguishing between different pattern-formation mechanisms.