Optimality In Biology

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'''Foraging strategy - Optimal Foraging: A Selective Review of Theory and Tests.''' <cite>Pyke-TheQuarterlyReviewofBiology-1977</cite>: Beginning with Emlen (1966) and MacArthur and Pianka (1966) and extending through the last ten years, several authors have sought to predict the foraging behavior of animals by means of mathematical models. These models are very similar,in that they all assume that the fitness of a foraging animal is a function of the efficiency of foraging measured in terms of some "currency" (Schoener, 1971) -usually energy- and that natural selection has resulted in animals that forage so as to maximize this fitness. As a result of these similarities, the models have become known as "optimal foraging models"; and the theory that embodies them, "optimal foraging theory." The situations to which optimal foraging theory has been applied, with the exception of a few recent studies, can be divided into the following four categories: (1) choice by an animal of which food types to eat (i.e., optimal diet); (2) choice of which patch type to feed in (i.e., optimal patch choice); (3) optimal allocation of time to different patches; and (4) optimal patterns and speed of movements. In this review we discuss each of these categories separately, dealing with both the theoretical developments and the data that permit tests of the predictions. The review is selective in the sense that we emphasize studies that either develop testable predictions or that attempt to test predictions in a precise quantitative manner. We also discuss what we see to be some of the future developments in the area of optimal foraging theory and how this theory can be related to other areas of biology. Our general conclusion is that the simple models so far formulated are supported are supported reasonably well by available data and that we are optimistic about the value both now and in the future of optimal foraging theory. We argue, however, that these simple models will requre much modification, espicially to deal with situations that either cannot easily be put into one or another of the above four categories or entail currencies more complicated that just energy.
'''Foraging strategy - Optimal Foraging: A Selective Review of Theory and Tests.''' <cite>Pyke-TheQuarterlyReviewofBiology-1977</cite>: Beginning with Emlen (1966) and MacArthur and Pianka (1966) and extending through the last ten years, several authors have sought to predict the foraging behavior of animals by means of mathematical models. These models are very similar,in that they all assume that the fitness of a foraging animal is a function of the efficiency of foraging measured in terms of some "currency" (Schoener, 1971) -usually energy- and that natural selection has resulted in animals that forage so as to maximize this fitness. As a result of these similarities, the models have become known as "optimal foraging models"; and the theory that embodies them, "optimal foraging theory." The situations to which optimal foraging theory has been applied, with the exception of a few recent studies, can be divided into the following four categories: (1) choice by an animal of which food types to eat (i.e., optimal diet); (2) choice of which patch type to feed in (i.e., optimal patch choice); (3) optimal allocation of time to different patches; and (4) optimal patterns and speed of movements. In this review we discuss each of these categories separately, dealing with both the theoretical developments and the data that permit tests of the predictions. The review is selective in the sense that we emphasize studies that either develop testable predictions or that attempt to test predictions in a precise quantitative manner. We also discuss what we see to be some of the future developments in the area of optimal foraging theory and how this theory can be related to other areas of biology. Our general conclusion is that the simple models so far formulated are supported are supported reasonably well by available data and that we are optimistic about the value both now and in the future of optimal foraging theory. We argue, however, that these simple models will requre much modification, espicially to deal with situations that either cannot easily be put into one or another of the above four categories or entail currencies more complicated that just energy.
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==chromosome loss rate==  
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==Chromosome loss rate==  
'''The optimal rate of chromosome loss in cancer'''
'''The optimal rate of chromosome loss in cancer'''
<cite>Komarova-PNAS-2004 Komarova-CellCycle-2004</cite>: Many cancers are characterized by a high degree of aneuploidy, which is believed to be a result of chromosomal instability (CIN). The precise role of CIN in cancer is still the matter of a heated debate. We present a quantitative framework for examining the selection pressures acting on populations of cells and weigh the "pluses" and "minuses" of CIN from the point of view of a selfish cell. We calculate the optimal rate of chromosome loss assuming that cancer is initiated by inactivation of a tumor suppressor gene followed by a clonal expansion. The resulting rate, p* = 10(-2)per cell division per chromosome, is similar to that obtained experimentally by Lengauer et al. (1997). Our analysis further suggests that CIN does not arise simply because it allows a faster accumulation of carcinogenic mutations. Instead, CIN must arise because of alternative reasons, such as environmental factors, epigenetic events, or as a direct consequence of a tumor suppressor gene inactivation. The increased variability alone is not a sufficient explanation for the presence of CIN in the majority of cancers.
<cite>Komarova-PNAS-2004 Komarova-CellCycle-2004</cite>: Many cancers are characterized by a high degree of aneuploidy, which is believed to be a result of chromosomal instability (CIN). The precise role of CIN in cancer is still the matter of a heated debate. We present a quantitative framework for examining the selection pressures acting on populations of cells and weigh the "pluses" and "minuses" of CIN from the point of view of a selfish cell. We calculate the optimal rate of chromosome loss assuming that cancer is initiated by inactivation of a tumor suppressor gene followed by a clonal expansion. The resulting rate, p* = 10(-2)per cell division per chromosome, is similar to that obtained experimentally by Lengauer et al. (1997). Our analysis further suggests that CIN does not arise simply because it allows a faster accumulation of carcinogenic mutations. Instead, CIN must arise because of alternative reasons, such as environmental factors, epigenetic events, or as a direct consequence of a tumor suppressor gene inactivation. The increased variability alone is not a sufficient explanation for the presence of CIN in the majority of cancers.

Revision as of 09:49, 21 December 2007

Contents

Optimality In Biology – a comprehensive collection of annotated examples

Motivation and definition

Optimality – the property of a system to maximize or minimize some function under given constraints – has been a central concept in many fields such as physics, computer science and engineering. In the realm of biology, natural selection leads to exquisite functional life forms all abiding to the laws of physics and chemistry yet show remarkable adaptation to the surrounding conditions. One manifestation of this process is that some characteristics of organisms can be shown to be close to optimally adapted to the constraints of their environment. This website and annotated collection aims to serve as a source of examples that will help discuss and disseminate this form of studying biological processes and inspire the analysis of other biological phenomena using these tools and perspectives.

In many respects the emphasis is on the constrains rather than on the issue of optimality per se, as eloquently framed by Parker and Maynard-Smith: “Optimization models help us to test our insight into the biological constraints that influence the outcome of evolution. They serve to improve our understanding about adaptations, rather than to demonstrate that natural selection produces optimal solutions.” [1]. We encourage everyone interested in this fascinating subject to add examples, comments and join the discussion either by directly editing these pages or by communicating them through email (ron_milo@hms.harvard.edu) and we will add them.

Examples

(we aim to have a concise description of what was achieved in each set of examples. Currently there is the abstract of the respective papers):

Level of protein expression

Level of protein expression – Optimality and evolutionary tuning of the expression level of a protein. [2, 3, 4]: Different proteins have different expression levels. It is unclear to what extent these expression levels are optimized to their environment. Evolutionary theories suggest that protein expression levels maximize fitness, but the fitness as a function of protein level has seldom been directly measured. To address this, we studied the lac system of Escherichia coli, which allows the cell to use the sugar lactose for growth. We experimentally measured the growth burden due to production and maintenance of the Lac proteins (cost), as well as the growth advantage (benefit) conferred by the Lac proteins when lactose is present. The fitness function, given by the difference between the benefit and the cost, predicts that for each lactose environment there exists an optimal Lac expression level that maximizes growth rate. We then performed serial dilution evolution experiments at different lactose concentrations. In a few hundred generations, cells evolved to reach the predicted optimal expression levels. Thus, protein expression from the lac operon seems to be a solution of a cost-benefit optimization problem, and can be rapidly tuned by evolution to function optimally in new environments.

Growth rate on different carbon sources

Growth rate on different carbon sources - Escherichia coli K-12 undergoes adaptive evolution to achieve in silico predicted optimal growth [5]: Annotated genome sequences can be used to reconstruct whole-cell metabolic networks. These metabolic networks can be modeled and analyzed (computed) to study complex biological functions. In particular, constraints-based in silico models have been used to calculate optimal growth rates on common carbon substrates, and the results were found to be consistent with experimental data under many but not all conditions. Optimal biological functions are acquired through an evolutionary process. Thus, incorrect predictions of in silico models based on optimal performance criteria may be due to incomplete adaptive evolution under the conditions examined. Escherichia coli K-12 MG1655 grows sub-optimally on glycerol as the sole carbon source. Here we show that when placed under growth selection pressure, the growth rate of E. coli on glycerol reproducibly evolved over 40 days, or about 700 generations, from a sub-optimal value to the optimal growth rate predicted from a whole-cell in silico model. These results open the possibility of using adaptive evolution of entire metabolic networks to realize metabolic states that have been determined a priori based on in silico analysis.

The genetic code

The genetic code - Evolution and multilevel optimization of the genetic code [6]: The discovery of the genetic code was one of the most important advances of modern biology. But there is more to a DNA code than protein sequence; DNA carries signals for splicing, localization, folding, and regulation that are often embedded within the protein-coding sequence. In this issue, Itzkovitz and Alon show that the specific 64-to-20 mapping found in the genetic code may have been optimized for permitting protein-coding regions to carry this extra information and suggest that this property may have evolved as a side benefit of selection to minimize the negative effects of frameshift errors.

Photosynthetic antenna

Photosynthetic antenna - Position and orientation of the chlorophyll pigments - Optimization and evolution of light harvesting in photosynthesis: the role of antenna chlorophyll conserved between photosystem II and photosystem I. [7]: The efficiency of oxygenic photosynthesis depends on the presence of core antenna chlorophyll closely associated with the photochemical reaction centers of both photosystem II (PSII) and photosystem I (PSI). Although the number and overall arrangement of these chlorophylls in PSII and PSI differ, structural comparison reveals a cluster of 26 conserved chlorophylls in nearly identical positions and orientations. To explore the role of these conserved chlorophylls within PSII and PSI we studied the influence of their orientation on the efficiency of photochemistry in computer simulations. We found that the native orientations of the conserved chlorophylls were not optimal for light harvesting in either photosystem. However, PSII and PSI each contain two highly orientationally optimized antenna chlorophylls, located close to their respective reaction centers, in positions unique to each photosystem. In both photosystems the orientation of these optimized bridging chlorophylls had a much larger impact on photochemical efficiency than the orientation of any of the conserved chlorophylls. The differential optimization of antenna chlorophyll is discussed in the context of competing selection pressures for the evolution of light harvesting in photosynthesis.

Chemotactic behavior

Chemotactic response function - The bacterial chemotactic response reflects a compromise between transient and steady-state behavior. [8, 9]: Swimming bacteria detect chemical gradients by performing temporal comparisons of recent measurements of chemical concentration. These comparisons are described quantitatively by the chemotactic response function, which we expect to optimize chemotactic behavioral performance. We identify two independent chemotactic performance criteria: In the short run, a favorable response function should move bacteria up chemoattractant gradients; in the long run, bacteria should aggregate at peaks of chemoattractant concentration. Surprisingly, these two criteria conflict, so that when one performance criterion is most favorable, the other is unfavorable. Because both types of behavior are biologically relevant, we include both behaviors in a composite optimization that yields a response function that closely resembles experimental measurements. Our work suggests that the bacterial chemotactic response function can be derived from simple behavioral considerations and sheds light on how the response function contributes to chemotactic performance.

Neuronal wiring

Neuronal wiring - Wiring optimization can relate neuronal structure and function. [10]: We pursue the hypothesis that neuronal placement in animals minimizes wiring costs for given functional constraints, as specified by synaptic connectivity. Using a newly compiled version of the Caenorhabditis elegans wiring diagram, we solve for the optimal layout of 279 nonpharyngeal neurons. In the optimal layout, most neurons are located close to their actual positions, suggesting that wiring minimization is an important factor. Yet some neurons exhibit strong deviations from "optimal" position. We propose that biological factors relating to axonal guidance and command neuron functions contribute to these deviations. We capture these factors by proposing a modified wiring cost function.

Foraging strategy

Foraging strategy - Optimal Foraging: A Selective Review of Theory and Tests. [11]: Beginning with Emlen (1966) and MacArthur and Pianka (1966) and extending through the last ten years, several authors have sought to predict the foraging behavior of animals by means of mathematical models. These models are very similar,in that they all assume that the fitness of a foraging animal is a function of the efficiency of foraging measured in terms of some "currency" (Schoener, 1971) -usually energy- and that natural selection has resulted in animals that forage so as to maximize this fitness. As a result of these similarities, the models have become known as "optimal foraging models"; and the theory that embodies them, "optimal foraging theory." The situations to which optimal foraging theory has been applied, with the exception of a few recent studies, can be divided into the following four categories: (1) choice by an animal of which food types to eat (i.e., optimal diet); (2) choice of which patch type to feed in (i.e., optimal patch choice); (3) optimal allocation of time to different patches; and (4) optimal patterns and speed of movements. In this review we discuss each of these categories separately, dealing with both the theoretical developments and the data that permit tests of the predictions. The review is selective in the sense that we emphasize studies that either develop testable predictions or that attempt to test predictions in a precise quantitative manner. We also discuss what we see to be some of the future developments in the area of optimal foraging theory and how this theory can be related to other areas of biology. Our general conclusion is that the simple models so far formulated are supported are supported reasonably well by available data and that we are optimistic about the value both now and in the future of optimal foraging theory. We argue, however, that these simple models will requre much modification, espicially to deal with situations that either cannot easily be put into one or another of the above four categories or entail currencies more complicated that just energy.

Chromosome loss rate

The optimal rate of chromosome loss in cancer [12, 13]: Many cancers are characterized by a high degree of aneuploidy, which is believed to be a result of chromosomal instability (CIN). The precise role of CIN in cancer is still the matter of a heated debate. We present a quantitative framework for examining the selection pressures acting on populations of cells and weigh the "pluses" and "minuses" of CIN from the point of view of a selfish cell. We calculate the optimal rate of chromosome loss assuming that cancer is initiated by inactivation of a tumor suppressor gene followed by a clonal expansion. The resulting rate, p* = 10(-2)per cell division per chromosome, is similar to that obtained experimentally by Lengauer et al. (1997). Our analysis further suggests that CIN does not arise simply because it allows a faster accumulation of carcinogenic mutations. Instead, CIN must arise because of alternative reasons, such as environmental factors, epigenetic events, or as a direct consequence of a tumor suppressor gene inactivation. The increased variability alone is not a sufficient explanation for the presence of CIN in the majority of cancers.

leaf size

Optimal Leaf Size in Relation to Environment [14]: The principle of optimal design (Rosen 1967) can be stated as follows. `Natural selection leads to organisms having a combination of form and function optimal for growth and reproduction in the environments in which they live.' This principle provides a general framework for the study of adaptation in plants and animals. The efficiency of water use by plants (Slatyer 1964) can be defined as grams of carbon dioxide assimilated per gram of water lost. Leaf temperatures, transpiration rates, and water-use efficiencies can be calculated for single leaves using well-established principles of heat and mass transfer. The calculations are complex, however, depending on seven independent variables such as air temperature, humidity and stomatal resistance. The calculations can be treated as artificial data in factorial design experiment. This technique is used to compare the sensitivity of the system response variables to changes in the independent variables, and to their interactions. The assumption is made (as a first approximation) that the optimal leaf size in a given environment is the size yielding the maximum water-use efficiency. This very simple assumption leads to predictions of trends in leaf size which agree well with the observed trends in diverse regions (tropical rainforest, desert, arctic, etc.). Specifically, the model predicts that large leaves should be selected for only in warm or hot environments with low radiation (e.g. forest floors in temperate and tropical regions). There are some plant forms and microhabitats for which observed leaf sizes disagree with the predictions of the simple model. Refinements are thus proposed to include more factors in the model, such as the temperature dependence of net photosynthesis. It is shown that these refinements explain much of the lack of agreement of the simpler model. One of the main roles of mathematical models in science is `to pose sharp questions' (Kac 1969). The present model suggests several speculative propositions, some of which would be difficult to prove experimentally. Others, whether true or not, can serve as a theoretical framework against which to compare experimental results. The propositions are as follows. (1) Every environment tends to select for leaf sizes increasing the efficiency of water utilization, that is, the ratio of CO_2 uptake to water loss. (2) Herbs are physiologically different from woody plants, in such a way that water-use efficiency has been more important in the evolution of the latter. (3) The stomatal resistance of a given leaf varies diurnally in such a way that the water-use efficiency of that leaf tends to be a maximum. (4) The larger the photosynthesizing surface of a desert succulent, the more likely it is to exhibit acid metabolism, with stomata open at night and closed during the day. (5) In arctic and alpine regions, the plant species whose carbohydrate metabolism is most severely limited by low temperatures are most likely to evolve a cushion form of growth. In addition to providing these testable hypotheses, the results of the model may be useful in other ways. For example, they should help plant breeders to alter water-use efficiencies, and they could help palaeobotanists interpret past climates from fossil floras.


More examples

  • Life history properties: Age of reproductive maturity, number of eggs in a clutch, etc. [15]
  • Codon usage and biases (Ref.)
  • Shapes that minimize drag (Ref. fish, fungi spores, birds?)
  • Prey interception strategy of bats (Ghose et al., PLOS Biology 2006)
  • Optimal virulence level (Jensen et al., PLOS Biology 2006)
  • Neural information transmission (Bialek 1997)
  • tRNA levels
  • morphogen gradients
  • photosynthesis wavelength
  • enzymes near the diffusion limit
  • Optimal metabolic network operation (“Systematic evaluation of objective functions for predicting intracellular fluxes in Escherichia coli” Robert Schuetz, Lars Kuepfer1 & Uwe Sauer Also Jens Nielsen, 2007)
  • Neuronal energetics - Simon Laughlin
  • Compound eye aperture size at the diffraction/resolution limit
  • Water usage efficiency - the opening of the stomata for maximal carbon fixation per water lost
  • Allocating leaf nitrogen - Allocating leaf nitrogen for the maximization of carbon gain: Leaf age as a control on the … C Field - Oecologia, 1983 - Springer; Maximizing daily canopy photosynthesis with respect to the leaf nitrogen allocation pattern in the,T Hirose, MJA Werger - Oecologia, 1987 - Springer; Trade-off Between Light-and Nitrogen-use Efficiency in Canopy Photosynthesis T HIROSE, FA BAZZAZ - Annals of Botany, 1998 - Annals Botany Co; Photosynthesis and nitrogen relationships in leaves of C 3 plants - JR Evans - Oecologia, 1989 - Springer; RESOURCE LIMITATION IN PLANTS AN ECONOMIC ANALOGY - AJ Bloom, FS Chapin III, HA Mooney - Ann. Rv. Ecol. Syst, 1985 - Annual Reviews
  • branching structure of the vascular tree - Optimal branching structure of the vascular tree, A Kamiya, T Togawa, Bulletin of Mathematical Biology, 1972
  • metabolism and fluxes - Principles of optimal metabolic network operation, Jens Nielsen; Schuetz R, Kuepfer L, Sauer U (2007) Systematic evaluation of objective functions for predicting intracellular fluxes in Escherichia coli. Mol Syst Biol 3: 119
  • other - A theory of optimal differential gene expression W Liebermeister, E Klipp, S Schuster, R Heinrich - BioSystems, 2004 - Elsevier


References

  1. Parker G.A. and Smith J.M. Optimality theory in evolutionary biology. Nature 1990 27-33. [Parker-Nature-1990]
  2. Dekel E and Alon U. . pmid:16049495. PubMed HubMed [Dekel-Nature-2005]
  3. Uri Alon. An introduction to systems biology. Boca Raton, FL: Chapman & Hall/CRC, 2007. isbn:9781584886426. [Alon-Introduction-Systems]
  4. Tomer Kalisky, Erez Dekel and Uri Alon Cost–benefit theory and optimal design of gene regulation functions Phys. Biol. 4 (2007) 229–245 [Kalisky-PhysicalBiology-2007]
  5. Ibarra RU, Edwards JS, and Palsson BO. . pmid:12432395. PubMed HubMed [Ibara-Nature-2002]
  6. Bollenbach T, Vetsigian K, and Kishony R. . pmid:17351130. PubMed HubMed [Bollenbach-GenomeResearch-2007]
  7. Vasil'ev S and Bruce D. . pmid:15486105. PubMed HubMed [Vasilev-PlantCell-2004]
  8. Clark DA and Grant LC. . pmid:15967993. PubMed HubMed [Clark-PNAS-2005]
  9. SP Strong, B Freedman, W Bialek, R Koberle Adaptation and optimal chemotactic strategy for E. coli. - Physical Review E, 1998 [Strong-PRE-1998]
  10. Chen BL, Hall DH, and Chklovskii DB. . pmid:16537428. PubMed HubMed [Chen-PNAS-2006]
  11. G. H. Pyke, H. R. Pulliam, E. L. Charnov Optimal Foraging: A Selective Review of Theory and Tests. The Quarterly Review of Biology, Vol. 52, No. 2 (1977), pp. 137-154 [Pyke-TheQuarterlyReviewofBiology-1977]
  12. Komarova NL and Wodarz D. . pmid:15105448. PubMed HubMed [Komarova-PNAS-2004]
  13. Komarova N. . pmid:15190212. PubMed HubMed [Komarova-CellCycle-2004]
  14. D. F. Parkhurst, O. L. Loucks Optimal Leaf Size in Relation to Environment The Journal of Ecology, Vol. 60, No. 2 (Jul., 1972), pp. 505-537 doi:10.2307/2258359 [Parkhurst-JournalEcology-1972]
  15. Stephen C. Stearns. The evolution of life histories. Oxford; Oxford University Press, 1992. isbn:0198577419. [Stearns-Evolution-Life]
All Medline abstracts: PubMed HubMed
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