Thursday, September 20, 2007

Evo-Devo: Innovation and Robustness in Evolution

When I first read the paper by Ciliberti et al. (2007) I was disappointed. On the surface, the paper seems to be addressing an important issue in evolutionary theory; namely, how can you get significant innovation in light of the fact that most biological systems resist change? On closer reading, however, it seemed more complicated than that. The authors were actually dealing with a phenomenum called "robustness." This is a popular description of a simple fact—the fact that many mutations are neutral so that there can be many variants of a protein that all carry out the same function. This has been known for decades.

The people who use the word "robustness" tend to elevate it to a level of significance that makes me nervous. Furthermore, they rarely use the term "random genetic drift" or "accident" in their papers, giving the impression that "robustness" is an adaptation that favors evolution.

There's much to criticize in the field of evolutionary developmental biology or evo-devo. Some of the "theories" are little more than wide-eyed speculation. I'm thinking particularly of The Plausibility of Life by Marc Kirschner and John Gehart.
Animal Chauvinism
That's one of the problems I have with this paper. The other problem is that it's a modeling paper. The authors create a model of evolution and demonstrate that their model produces systems that evolve. I have a problem with these models. While a mathematical model is useful to show that a mechanism can work, it does not prove that it does work.

Let me give a quick example to show you why I'm skeptical of claims by modelers. It is possible to model a Lamarckian process where species inherit acquired characteristics. The result will be evolution but that does not mean that the inheritance of acquired characteristics is a real mechanism of evolution. This point is not always made clearly in papers that describe mathematical models of evolution. To often, the fact that the model produces evolution is taken as evidence that the assumptions in the model are correct and it is an accurate representation of real biological evolution. This is the same problem with just-so stories [Just-So Stories].

Let's see how Ciliberti et al. (2007) set up their experiments in the introduction to the paper.
Biologists increasingly realize that genetic systems need to be robust to both genetic and nongenetic change (7–14). Robustness means that a system keeps performing its function in the face of perturbations. For example, many proteins can continue to catalyze chemical reactions, regulate transcription, communicate signals, and serve other roles despite mutations changing many amino acids; regulatory gene networks continue to function despite noisy expression of their constituent genes; embryos continue to develop normally even when faced with substantial environmental variation. Mutational robustness means that a system produces little phenotypic variation when subjected to genotypic variation caused by mutations. At first sight, such robustness might pose a problem for evolutionary innovation, because a robust system cannot produce much of the variation that can become the basis for evolutionary innovation.
The language sounds a little strange to me but I soon realized that there were many other authors who talked about "robustness" in this way. To me, the fact that there's neutral genetic variation in a population is just a natural consequence of chance mutation and random genetic drift. I don't see why biologists think that systems "need" to be robust and I don't see why the presence of neutral variation poses a "problem" for innovative change. It's perfectly acceptable to have beneficial mutations occurring on a background of neutral variation.

The "problem" seems to be more serious for evolutionary developmental (evo-devo) biologists than for others. It has given rise to much speculation about the evolution of evolvability. If you are interested in that sort of thing you should read the book The Plausibility of Life by Marc Kirschner and John Gelhart. (Warning, the contents may not be suitable for pluralists.)

The authors of the paper (Ciliberti et al.) claim that far from being a "problem" the existence of neutral variation is actually required for innovative evolution to occur.
As we shall see, there is some truth to this appearance, but it is in other respects flawed. Robustness and the ability to innovate cannot only coexist, but the first may be a precondition for the second.
This is pretty much where I stopped reading the first time. However, Michael White over on Adaptive Complexity has highlighted this paper in a posting put up yesterday [Evolution's Balancing Act]. This suggest that the paper resonates with some evolutionary biologists and piques my interest.

The paper describes a model of an evolutionary system. It happens to be gene regulatory networks but it could be just about anything. Ciliberti et al. (2007) show that if you have a single system with no variation then the possibility for innovative change is limited. On the other hand, if you have a robust system where there are many different variants—in different species—then there are more pathways to innovative change. Seems like a pretty trivial conclusion to me. It's the sort of thing Sewell Wright was talking about (Wright, 1932).
The course of evolution through the general field [adaptive landscape-LAM] is not controlled by direction of mutation and not directly by selection, except as conditions change, but by a trial and error mechanism consisting of a largely nonadaptive differentiation of local races (due to inbreeding and by occasional crossbreeding) and a determination of long time trend by intergroup selection.
The paper doesn't mention Wright, random genetic drift, or neutral mutations; although it does talk about neutral networks.

Instead, the paper seems to be fitting in with the evo-devo concepts of evolvability and facilitated variation. In other words the idea here seems to be getting very close to the concept that the variations in different species are selected because they increase the long term potential for innovative evolution. This is very different from what Wright was saying. He said—and I agree with him—that the variation is strictly accidental and just happens to provide potential for future evolution. The distinction is important for our understanding of evolution. Does evolution see into the future? Is there a hidden purpose?

Is "robustness" selected? I doubt that any of the authors would answer yes if the question was put directly but the paper certainly gives the impression that there's something positive going on. So does the description offered by Michael White when he says thing like,
Evolution carries out an incredibly tricky balancing act: the genetic program of a species has to be resistant to small changes, yet also susceptible to the adaptive remodeling of natural selection ....

So how does evolution maintain both stability and the potential for innovation?
This could be just metaphoric. The personification of "evolution" as acting to creat robustness may be excusable on that grounds. Nevertheless, a lot of this sort of language is creeping into the evo-devo literature and I wonder if it doesn't mean something more.


S. Ciliberti, s., Martin, O.C. and Wagner, A. (2007) Innovation and robustness in complex regulatory gene networks. Proc. Natl. Acad. Sci. (USA) 104:13591-13596. Abstract

Wright, S. (1932) The roles of mutation, selection, inbreeding, crossbreeding, and selection in evolution. Proc. VI Intl. Cong. Genet. 1:356-366.

14 comments:

  1. Gerhart is an adaptationist. The kind of "genius" who finds it fit to ignore solid data to favor adaptationist speculation; for example, he questioned the dorso-ventral inversion of the body axis in deuterostomes (but new data quite unsriprisingly proved him worng and he has HAD to take back some of his "criticism").
    Why do adaptationists hit the pages of PNAS so often? Some of their articles there are truly ridiculous.

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  2. The problem of the adaptaionists with the d-v inversion is: why? since they cannot make an adaptationist story for this change without sounding silly, they doubt the change itself. Same thing with the "homeotic frameshift" of digital identity in birds. No matter how well documented a change is, adaptationists feel they can question it they can't figure an "adaptive value" for it. They will say it has no "truly evolutionary" explanation. Darlings.
    There are better and worse researchers in evo-devo, as in any field.

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  3. Thanks for spelling out so clearly the issues I've only been grumbling about.

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  4. Neutralism is the enabler and facilitator of adaptive evolution. For example, as I wrote on the "Genomics is dead" thread:

    "The same is true of drift of neutral genes, biomolecules, and traits - as someone pointed out on another thread, they permit random walks across the adaptive landscape, exploring new potentials for adaptations. In the long run, neutralism is, like systems phenomena, an enabler of adaptation through natural selection. ...

    Actually, all drift, not just drift in neutral entities, has that adaptation-facilitating property of random exploration of adaptive landscapes. It is also important to consider that the status of neutrality is often conditional on the organism and the environment, and so can become non-neutral."

    If there were no neutrality (or near-neutrality), populations would be more likely to be haplessly stuck to local optima, waiting around for powerful mutations to nudge them. Regulatory networks would have "little wiggle room" for change.

    I think the teleological language that Dr. Moran objects to refers to the consequences of higher level selection (clade selection). It only sounds teleological because of the associations of these terms.

    Tupaia

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  5. BTW, nice post larry; and I agree. It's no coincidence these people do not give drift it's proper due. They are taking an ultimately adaptationist stance

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  6. And how does deuterostome dorso-ventral inversion refute adaptationism? Because the origin of a developmental change (whatever the scale of its effect) is not itself adaptive? Where in Darwinism or the Modern Synthesis is written that it has to be? Mutations and phenocopies are not adaptive in origin. Selection that modifies and builds on mutations that alter traits or genetically assimilates induced changes does have adaptive consequences. This is very elementary evolutionary biology.

    Tupaia

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  7. However, let me add that a good deal of developmental plasticity which is material for genetic facilitation is often the adaption of past selection - the reaction norm is just another trait, and much of it is adaptive.

    However, a novel phenocopy of a macromutation is likely not adaptive in origin. Of course, once selection shapes it, it is adaptive.

    Tupaia

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  8. There you go. Yet despite this, some think taht not having an adatpaionist story is reason enough to QUESTION the veracity of well documented changes. See, tupaia? There IS such a thing as runaway adaptationism

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  9. Developmental modularity, robusticity, and deconstraint allow for the viability of macromutants (topological, homeotic, segment number etc.) and macro-phenocopies. Lineages with epigenetic programs that have high deconstraint - and hence more evolvable - are favored by clade selection.

    Think of Kimura, Fisher, and Goldschmidt as being on a continuum - many neutral and near-neutral mutations, few beneficial mutations, very rare beneficial macromutations. All are important in providing the material basis of evolution. Complex adaptations and phyletic traits arise from both gradual selective accumulation of mutations of small effect and selectively modified macromutations (and combinations of these). Baldwinian processes have a major role in directing the course of evolutionary change.

    Tupaia

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  10. Thanks, very instructive.

    First I didn't get what the problem with robustness vs structural change was. After all, in physical systems a robust local minima can topologically be moved to be aggregated with another or disappear in a "catastrophe" as René Thom so pictorially named it.

    But the complication here is of course the constraint of viability. I think I got a glimpse into what "higher level selection" is (selection by extinction on pool of species traits analogous to selection by death on pool of population traits (alleles) ?) and its connection to "evolution of evolvability".

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  11. All very interesting: Can evolution evolve systems that are more evolvable? This is one of those recognizable meta-questions similar to, for example; Can we write a program that writes programs? Always very ‘difficult’ such meta ‘problems’, I suspect, are not in the range of evolution as currently conceived; I doubt that it is vigorous enough in terms of its ‘change ringing processes’ (mutation) and ‘testing’ (selecting) to ‘solve’ them. (that’s an amateur’s opinion I hasten to add)

    The personification of evolution? There are, I believe, isomorphisms linking evolution, computation, and thinking that make such personifications difficult to avoid.

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  12. All and any use of facilitation in evolutionary biology seems to point to a muddle in thinking.

    Anyway, can anyone explain to me what 'genetic facilitation' might be?

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  13. Here's an interesting recent paper. It's not really saying anything particularly startling but it's interesting nonetheless and worth a read:

    Bloom, J.D. et al. (2007) Neutral genetic drift can alter promiscuous protein functions, potentially aiding functional evolution. Biology Direct, 2, Art 17.

    Background: Many of the mutations accumulated by naturally evolving proteins are neutral in the sense that they do not significantly alter a protein's ability to perform its primary biological function. However, new protein functions evolve when selection begins to favor other, "promiscuous" functions that are incidental to a protein's original biological role. If mutations that are neutral with respect to a protein's primary biological function cause substantial changes in promiscuous functions, these mutations could enable future functional evolution.

    Results: Here we investigate this possibility experimentally by examining how cytochrome P450 enzymes that have evolved neutrally with respect to activity on a single substrate have changed in their abilities to catalyze reactions on five other substrates. We find that the enzymes have sometimes changed as much as four-fold in the promiscuous activities. The changes in promiscuous activities tend to increase with the number of mutations, and can be largely rationalized in terms of the chemical structures of the substrates. The activities on chemically similar substrates tend to change in a coordinated fashion, potentially providing a route for systematically predicting the change in one activity based on the measurement of several others.

    Conclusion: Our work suggests that initially neutral genetic drift can lead to substantial changes in protein functions that are not currently under selection, in effect poising the proteins to more readily undergo functional evolution should selection favor new functions in the future.

    http://www.biology-direct.com/content/2/1/17

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  14. Whilst I remember, also check out another recent paper.

    Bazykin, G.A. et al. (2007) Extensive parallelism in protein evolution. Biology Direct, 2, 20.

    Background

    Independently evolving lineages mostly accumulate different changes, which leads to their gradual divergence. However, parallel accumulation of identical changes is also common, especially in traits with only a small number of possible states.
    Results

    We characterize parallelism in evolution of coding sequences in three four-species sets of genomes of mammals, Drosophila, and yeasts. Each such set contains two independent evolutionary paths, which we call paths I and II. An amino acid replacement which occurred along path I also occurs along path II with the probability 50-80% of that expected under selective neutrality. Thus, the per site rate of parallel evolution of proteins is several times higher than their average rate of evolution, but still lower than the rate of evolution of neutral sequences. This deficit may be caused by changes in the fitness landscape, leading to a replacement being possible along path I but not along path II. However, constant, weak selection assumed by the nearly neutral model of evolution appears to be a more likely explanation. Then, the average coefficient of selection associated with an amino acid replacement, in the units of the effective population size, must exceed ~0.4, and the fraction of effectively neutral replacements must be below ~30%. At a majority of evolvable amino acid sites, only a relatively small number of different amino acids is permitted.
    Conclusions

    High, but below-neutral, rates of parallel amino acid replacements suggest that a majority of amino acid replacements that occur in evolution are subject to weak, but non-trivial, selection, as predicted by Ohta's nearly-neutral theory.

    http://www.biology-direct.com/content/2/1/20/abstract

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