Expected Preparations:

  Metabolism:
Enzymatic catalysis and control; Reaction sequences and pathways; Catabolic- and anabolic pathways; Chemiosmotic coupling.
  Cell cycle:
Replication control and mechanism; Phases of the cell-cycle; Checkpoints and apoptosis.
  [FND-MAT]
Graphs_and_networks
 
  If you are not already familiar with the prior knowledge listed above, you need to prepare yourself from other information sources.   The units listed above are part of this course and contain important preparatory material.  

Keywords: Systems Models

Objectives:

This unit will …

  • … introduce a definition of biological systems;

  • … review facts and concepts of the yeast G1/S cell cycle switch to illustrate the building blocks of a functional architecture of this system;

  • … present examples of how this system is presented in different databases;

  • … teach how to apply reverse engineering principles, guided by the concept of a “system architecture”, to categorize system components, define their functional relationships, and illustrate categories and functions in an informative diagram;

Outcomes:

After working through this unit you …

  • … can identify key components of the yeast G1/S cell cycle switch by name and role;

  • … are familar with concepts of systems modelling;

  • … can abstract and organize factual knowledge to a sytems architecture diagram.


Deliverables:

Time management: Before you begin, estimate how long it will take you to complete this unit. Then, record in your course journal: the number of hours you estimated, the number of hours you worked on the unit, and the amount of time that passed between start and completion of this unit.

Journal: Document your progress in your Course Journal. Some tasks may ask you to include specific items in your journal. Don’t overlook these.

Insights: If you find something particularly noteworthy about this unit, make a note in your insights! page.


Evaluation:

NA: This unit is not evaluated for course marks.

Contents

The functional composition of individual biomolecules to “systems” faces challenges from incomplete data for “bottom up” approaches, and incomplete knowledge for “top down” approaches. This unit discusses the issues, explains the concept of reverse engineering higher order functions from basic components and demonstrates strategies for architectural modelling of systems.

 

A theory can be proved by an experiment; but no path leads from experiment to the birth of a theory. : (Variously attributed to Albert Einstein and Manfred Eigen)

 

Systems biology is about systems … but what is a system, anyway? Definitions abound, the recurring theme is that of connected “components” forming a complex “whole”. Complexity describes the phenomenon that properties of components can depend on the “context” of a component; the context is the entire system. That fact that it can be meaningful to treat such a set of components in isolation, dissociated from their other environment, tells us that not all components of biology are connected to the same degree. Some have many, strong, constant interactions (often these are what we refer to “systems”), others have few, weak, sporadic interactions and thus can often be dissociated in analysis. Given the fact that complex biological components can be perturbed by any number of generic environmental influences as well as specific modulating interactions, it is non-trivial to observe that we can in many cases isolate some components or sets of components and study them in a meaningful way. A useful mental image is that of clustering in datasets: even if we can clearly define a cluster as a number of elements that are strongly connected to each other, that usually still means some of these elements also have some connections with elements from other clusters. Moreover, our concepts of systems is often hierarchical, discussing biological phenomena in terms of entities or components, subsystems, systems, supersystems … as well, it often focusses on particular dimensions of connectedness, such as physical contact, in the study of complexes, material transformations, in the study of metabolic systems, or information flow, in the study of signalling systems and their higher-order assemblies in control and development.

At the end of the day, a biological system is a conceptual construct, a model we use to make sense of nature; nature however, ever pragmatical, knows nothing of systems.

In this sense systems biology could be dismissed as an artificial academic exercise, semantics, even molecular mysticism, if you will (and some experimentalists do take this position), IF systems biology were not curiously successful in its predictions. For example, we all know that metabolism is a network, crosslinked at every opportunity; still, the concept of pathways appears to correlate with real, observable properties of metabolite flux in living cells. Nature appears to prefer constructing components that interact locally, complexes, modules and systems, in a way that encapsulates their complex behaviour, rather than leaving them free to interact randomly with any other number of components in a large, disordered bag.

The mental construct of a “system” thus provides a framework for concepts that describe the functional organization of biological components.

 

Task…

 

Task…

Draw a system architecture diagram1 to represent the function of either * a water canister (cf. the image at the side); * a bicycle; * an anteater; * a hockey puck; * F1Fo-ATP Synthase; * a desk light; or * a cookbook.

Prepare your diagram by clearly defining and listing purpose, input, output and interfaces, feedback control and other structural and behavioural elements. Draw a draft on a separate piece of paper first, then prepare a legible sketch of your diagram. Don’t overcomplicate your diagram: 10 to 15 elements will be plenty.

A Google Doc with a systems architecture template is linked here. You can access it and make a copy for your own use.

(Water_canister.jpg)

 

Questions, comments

If in doubt, ask! If anything about this contents is not clear to you, do not proceed but ask for clarification. If you have ideas about how to make this material better, let’s hear them. We are aiming to compile a list of FAQs for all learning units, and your contributions will count towards your participation marks.

Improve this page! If you have questions or comments, please post them on the Quercus Discussion board with a subject line that includes the name of the unit.

References

Page ID: BIN-SYS-Concepts

Author:
Boris Steipe ( <boris.steipe@utoronto.ca> )
Created:
2017-08-05
Last modified:
2022-09-14
Version:
1.1
Version History:
–  1.1 Expanded
–  1.0 First live version
–  0.1 First stub
Tagged with:
–  Unit
–  Live
–  Has lecture slides
–  Contains images

 

[END]


  1. Some of these were the topic of an in-class quiz in 2016, with an alloted time of 15 minutes. Try hard not to take longer.↩︎