Developmental Biology Concepts on Cyber Entities Evolution - PowerPoint PPT Presentation

1 / 23
About This Presentation
Title:

Developmental Biology Concepts on Cyber Entities Evolution

Description:

Developmental Biology Concepts on Cyber Entities Evolution. Kawai Chan. chankw_at_uci.edu. Introduction ... single fertilized egg divides to a huge number of cells ... – PowerPoint PPT presentation

Number of Views:31
Avg rating:3.0/5.0
Slides: 24
Provided by: P357
Category:

less

Transcript and Presenter's Notes

Title: Developmental Biology Concepts on Cyber Entities Evolution


1
Developmental Biology Concepts on Cyber Entities
Evolution
  • Kawai Chan
  • chankw_at_uci.edu

2
Introduction
  • All biological organisms are the product of the
    interplay of genetics, evolution (dynamic) and
    developmental processes (static)
  • We can apply these concepts on the Bionet to
    evolve the CEs to increase the behavioral
    diversity

3
Dynamic Diversity Development
  • Currently, we only use the dynamic scheme to
    generate CEs behavioral diversity
  • Mutation
  • Crossover
  • The disadvantage of this scheme is the CEs need a
    trial and error period to evolve to be fully
    functional

4
Static Diversity Development
  • We would like to shorten the trial and error
    period by implementing the static scheme
  • Developmental biology

5
What is Developmental biology?
  • Developmental biology is a biological research
    field that explores
  • how a single fertilized egg divides to a huge
    number of cells and how they autonomously
    specialize in structure and functionality.
  • e.g. A human body consists of 60 trillion cells
    (254 types), each of which has different
    structure and functionality.
  • how cells gradually form a complex pattern.
  • i.e. how they decide their position in an adult
    body
  • e.g. nail at the tip of a finger

6
Important Developmental Processes
  • Gene Regulation
  • Cell Differentiation
  • Cell Lineage
  • Cell Induction
  • Positional Information by Morphogenetic Gradients
  • Cell Division and Cell Death
  • Cell Adhesion and Cell Migration

7
Gene Regulation
  • Two cells are different if they have different
    subsets of active gene
  • The differences between cells are emergent and
    can be controlled
  • The activity of gene is regulated by the
    regulatory units
  • Regulatory units (cis-regulators)
  • Represent a specific DNA region
  • Transcription factors (trans-regulators)
  • Represent some soluble body fluid to bind with
    cis-regulators

8
Regulatory units
  • Regulatory units are like switches for the
    specific cells
  • The on and off states of the switches are
    influenced by
  • The affinity between cis- and trans-regulators
  • The concentration of trans-regulators
  • The interactions of all the proteins which are
    necessary the transcription of a gene by
    polymerases
  • Auto catalytic regulation of the gene once it is
    activated

9
Cell Differentiation
  • To create different cell types
  • Two cells are different if they have different
    subsets of active gene in genome
  • There are two types of differentiation
  • Cell Lineage
  • Affected by intracellular factors
  • Cell Induction
  • Affected by signals from other cells

10
Positional Information
  • During development, the positions of cell are
    informed by a concentration gradient of a
    morphogen
  • Morphogen is a substance that can influence the
    development of cells
  • The morphogen can have different effects on
    different cells depending on
  • The affinity with the cis-regulators
  • The concentration of the morphogen
  • Morphogen are placed in the egg from parents when
    the cell is created

11
Cell division and Cell death
  • Different cells have different lifetime, e.g.
    neuron cells are not dividing while blood cells
    do
  • These differences depend on the different
    regulatory mechanisms. To stop a cell from
    dividing
  • Contact inhibition restricted by space
  • Growth factors affected by hormones
  • Purposed cell death is common in evolution, e.g.
    to avoid distinction

12
Cell Adhesion
  • In neurons, axon and dendrites are connected if
    they have a high enough affinity
  • These connections work together as a group, e.g.
    to transmit signals from hand to brain

13
Implementation
  • Store a gene as a string of integer for each CE
  • Two classes of genes are needed
  • Regulatory - switches
  • Structural functions

14
Implementation
  • The activation of a structural gene depend on the
    regulatory gene adjacent to it. Also, several
    regulatory genes can control one or more
    structural gene

15
Implementation
  • The transcription factor is used to calculate the
    affinity with the regulatory genes. When the
    affinity for a cell is higher than a specific
    value, the function of the cell is turned on
  • TFs are generated from CEs. TFs should also be
    stored in platforms to distribute the populations
    (e.g. A CE doesnt want to reproduce in a crowded
    platform). This is done by manipulating the
    formulas

16
Formulas
17
Implementation
  • Depending on which structural gene is activated,
    one of the following can occur
  • A TF is produced to regulate the gene activities
  • A cell adhesion molecule (CAM) is produced to
    connect cells to each other, if the affinity is
    high enough
  • A receptor is produced to regulate the
    communication between the cells
  • A artificial function like cell division, cell
    death, or searching can occur

18
Implementation
  • Cell differentiation depends on the signals that
    a CE receives, which may or may not have any
    effect on it depending on the affinity and the
    concentration of the substance
  • For Bionet, we will only use the method c, i.e.
    communicating through receptors

19
Implementation
  • Positional information (morphogen) is implemented
    with a string of integers as the transcription
    factor. These information is stored in each CE
    and platform. It can diffuse to other CEs
  • Both cell division and cell death can be
    implemented as structural genes
  • CEs should try to stay close with friends or
    those who provide reliable services

20
Whats next?
  • Decide what structural genes (functions) we need?
  • Consider including more information from CEs,
    e.g. body executable code, data behavior
    factors and weights
  • Consider applying mutation and crossover in the
    gene itself, i.e. to apply dynamic development on
    the static one, this may create a more diverse
    behaviors in a given time

21
Whats next?
  • Consider to have some totally static development
    and lifetime control of certain CEs. For
    example, security CE.
  • Investigate the difference between goal-setting
    evolution and random evolution.

22
References
  • Evolving Morphologies of Simulated 3D Organisms
    Based on Differential Gene Expression Peter
    Eggenberger
  • Cell Interactions as a Control Tool of
    Developmental Processes for Evolutionary Robotics
    Peter Eggenberger
  • Developmental Process inBionet Evolution
    Simulation - Jun Suzuki

23
The EndThank You
Write a Comment
User Comments (0)
About PowerShow.com