Developmental Biology

(and irreducible complexity)



 
 
 

"The plain fact is that despite all the talk of "master-control" genes, biologists still have no causal account of morphogenesis".
Evelyn Fox Keller, Biology and Philosophy, 14: 325, 1999.
 
 
"Describing developmental processes as robust is just another way of saying that they are so designed as to be able to resist (or to buffer) the inevitable physical and chemical vicissitudes that a developing egg encounters.  Indeed, ever since Driesch's inital observation of the phenomenon of regulation in 1891, one of the primary concerns of embryologists has been to understand this capacity of the embryo's to compensate for disturbances, i.e. its capacity to 'self-regulate'.  How is it done?  Long ago, the classical embryologist Hans Spemann argued for a "synergetical principle of development", or, as engineers called it, a principle of "double assurance".  As Spemann explained in his Silliman Lectures,
"The cautious engineer makes a construction so strong and durable that it will be able to stand a load which in practice it will never have to bear"
Recent work in molecular biology confirms Spemann's early intuition, providing increasing evidence for the extensive use in development of a variety of design principles resembling those used in engineering - "checkpoints," "back-up" (or "fail-safe") mechanisms, genetic redundancy, and parallel metabolic pathways."
Evelyn Fox Keller, Biology and Philosophy, 14: 325, 1999.
 


Modern physics operates under the Cosmological Principle, which roughly states that the Universe is the same in every place and in every direction.  Evolutionary biologists have long implicitly operated under a similar principle, which roughly states that the nature of the evolutionary process is the same at all times and places.  Paleontologists have broadened the range of processes, and attendant tempos, encompassed by this principle but the principle itself has rarely been questioned.  But the very uniqueness of the developmental homologies underlying all complex animals is a powerful argument against such evolutionary uniformitarianism.  There is every indication that the range of morphological innovation possible in the early Cambrian is simply not possible today - that the creation of the developmental hierarchies which are now so pervasive itself constrained subsequent architectural repatterning.

Douglas Erwin, Amer. Zool., 39:617, 1999.

 
 
 
 
 
Goal:
 
Review basic facts about development that challenge Darwinian macroevolution

 
 
 
 
 
Two major issues:
 
 
 
 
 
 
I.  Origin of developmental trajectories
 
Irreducible complexity?

The origin of developmental trajectories poses a challenge to neo-Darwinism.  It would appear that developmental trajectories cannot be built step-by-step, because a complete trajectory must be in place in order to result in a viable reproducing organism.  In other words, natural selection cannot act unless oganisms are sufficiently developed that they are able to reproduce.  For complex multicellular animals, a very complex trajectory is required to acheive a reproducing adult.  Where do such complex programs come from?  In developmental time, the information is present at the start, put in by the mother.  In evolutionary time, such an abrupt front-loading of information would amount to intelligent design.


 
 

II.  Variation in developmental trajectories
 

To change body plans, mutations must occur at the point in development where body plans are put into place.  But this often occurs right at the beginning.   Changes in body plan cannot be accomplished through the accumulation of late-acting mutations.  Arthur points out that neo-Darwinism does not take into account the structure of development.  Microevolutionary changes, which involve mutations of genes that act rather late in developmental time, cannot be extrapolated to account for the origin of new phyla.



 

 Development-1

from Wallace Arthur, "The Origin of Animal Body Plans"
 
 
 
 


 

 Development-2

from Wallace Arthur, "The Origin of Animal Body Plans"


"This appoach has important consequences for the neo-Darwinian view that major morphological differences between organisms from different higher taxa have been produced through the gradual accumulation of very small changes.  Specifically, while in a non-developmental approach it seems plausible that many small changes can indeed accumulate to give a larger one, in a developmentally explicit approach it is clear that many late changes can not accumulate to give an early one.  Thus, if taxonomically distant organisms differ right back to their early embyogenesis, as is often the case, the mutations involved in their evolutionary divergence did not involve the same genes as those involved in the typical speciation event, where usually the early embryogeneses of the daughter species concerned are virtually identical."
Wallace Arthur, The Origin of Animal Body Plans, pg 22.
 
 
Yet mutations that act early in development are almost always lethal.  The only counter example cited by Arthur is a class of mutations that changes the direction of coiling in snails (chirality in gastropods).
 
"The variations we see are not the ones Darwin's theory needs, and the ones it needs we do not see."
Paul Nelson, lecture at the "Nature of nature" conference, Baylor University, 1999.
 


Those genes "that are obviously variable within natural populations do not seem to lie at the base of the many major adaptive changes", while those that "seemingly do constitute the foundation of many, if not most, major adaptive changes apparently are not variable within natural populations".

John F. McDonald, "The Molecular Basis of Adaptation:  A Critical Review of Relevant Ideas and Observations,"  Annual Review of Ecology and Systematics 14 (1983):
77-102; pp. 92-93.

 
 

 Development-3

from Wallace Arthur, "The Origin of Animal Body Plans"
 
 
 
 
 
 
 
 

Three views of the role of development in evolutionary change
 
 

Development-4

from Wallace Arthur, "The Origin of Animal Body Plans"



 
 
 
 
 
 

Arthur's view:
The more complex the organism is the harder for individual mutational changes to produce a coordinated effect that stands a chance of being beneficial.  This is consistent with the notion of big experiments early and then progressively more restricted modifications.
 
 


For more on this subject see the following paper by Paul Nelson:

     http://www.iscid.org/nelsonchat.pdf

and discussion surrounding it:

http://www.iscid.org/paul-nelson-chat.php


 

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