Skip to main content
Log in

The generality of Constructive Neutral Evolution

  • Published:
Biology & Philosophy Aims and scope Submit manuscript

Abstract

Constructive Neutral Evolution (CNE) is an evolutionary mechanism that can explain much molecular inter-dependence and organismal complexity without assuming positive selection favoring such dependency or complexity, either directly or as a byproduct of adaptation. It differs from but complements other non-selective explanations for complexity, such as genetic drift and the Zero Force Evolutionary Law, by being ratchet-like in character. With CNE, purifying selection maintains dependencies or complexities that were neutrally evolved. Preliminary treatments use it to explain specific genetic and molecular structures or processes, such as retained gene duplications, the spliceosome, and RNA editing. Here we aim to expand the scope of such explanation beyond the molecular level, integrating CNE with Multi-Level Selection theory, and arguing that several popular higher-level selection scenarios are in fact instances of CNE. Suitably contextualized, CNE occurs at any level in the biological hierarchy at which natural selection as normally construed occurs. As examples, we focus on modularity in protein–protein interaction networks or “interactomes,” the origin of eukaryotic cells and the evolution of co-dependence in microbial communities—a variant of the “Black Queen Hypothesis” which we call the “Gray Queen Hypothesis”.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Notes

  1. Complexity is of course an onerous notion, highly dependent on context. Increases or decreases in its value might nevertheless be assessed—in terms of the interdependency of component parts or some product of the number of parts compared to part-types—with less ambiguity than assigning definite values to particular entities.

  2. Indeed, Koonin (2016) describes subfunctionalization as the clearest cases of the “evolutionary modality” of CNE.

  3. Gene duplication is also, of course, a source of “new genes” as when one duplicate acquires a novel function (“neofunctionalization”; Lynch and Conery 2000; Lynch and Force 2000) or when each of the duplicate pairs retains a subset of the functions of a their multi-functional common ancestor. Such “subfunctionalization” (Lynch and Conery 2000) comprises CNE as we define it below (pre-suppression followed by ratcheting).

  4. In the case of bacterial cells, Golding and Cox (2006) report that on time scales longer than a second, “the motion of the RNA molecule is dominated by interactions with obstacles in the medium surrounding it”—interactions we expect only to be amplified in more complexly compartmentalized eukaryotes.

  5. That such proteins are functional can be verified biochemically or by amino acid sequence similarity to homologous proteins in closely related organisms that do not have RNA editing.

  6. The Black Queen gets its name from the game of Hearts, where the goal of the game is to avoid being stuck with the queen of spades; likewise the goal is to avoid being stuck with certain costly genes. We term the CNE variant of the BQH the Gray Queen Hypothesis, to emphasize the likeness of both views, the absence of an all-or-nothing approach to selection, and since gray is a neutral colour.

  7. Something important is neglected thereby, and accepting CNE as a co-equal force to selection might help us recognize this level. It is after all this level that is the focal point of contemporary “systems biology” (Ideker et al. 2001).

  8. One could also cite so-called “moonlighting proteins”. These have well-known and likely more ancient functions, but have been “recruited” to serve additional important roles in basic transcriptional or translational processes (or as crystallins in the vertebrate eye and as tumor suppressors). Presumably these associations (even if subsequently “improved by positive selection”) began as fortuitous interactions with pre-existing cellular entities (Jeffery 2003).

  9. Moreover, as discussed in the next section, it may be a multi-species microbial community rather than a single prokaryotic cell that is appropriately compared to a eukaryotic cell.

Abbreviations

CNE:

Constructive Neutral Evolution

PPI:

Protein–protein interaction networks

ZFEL:

Zero-force evolutionary law

BQH:

Black Queen Hypothesis

GQH:

Gray Queen Hypothesis

References

  • Archibald JM, Logsdon JM, Doolittle WF (1999) Recurrent paralogy in the evolution of archaeal chaperonins. Curr Biol 9(18):1053–S6

    Article  Google Scholar 

  • Archibald JM, Logsdon JM Jr, Doolittle WF (2000) Origin and evolution of eukaryotic chaperonins: phylogenetic evidence for ancient duplications in CCT genes. Mol Biol Evol 17(10):1456–1466

    Article  Google Scholar 

  • Atay O, Skotheim JM (2014) Modularity and predictability in cell signaling and decision making. Mol Biol of the Cell 25(22):3445–3450

    Article  Google Scholar 

  • Bell G (2001) Neutral macroecology. Science 293(5539):2413–2418

    Article  Google Scholar 

  • Ben-David E, Burga A, Krugkyak L (2017) A maternal-effect selfish element in Caenorhabditis elegans. Science 356(6342):1051–1055

    Article  Google Scholar 

  • Bernstein H, Byerly HC, Hopf FA, Michod RE (1984) Origin of sex. J Theor Biol 110(3):323–351

    Article  Google Scholar 

  • Booth A, Doolittle WF (2015) Eukaryogenesis, how special really? Proc Natl Acad Sci USA 112(33):10278–10285

    Article  Google Scholar 

  • Bridgham JT, Ortlund EA, Thornton JW (2009) An epistatic ratchet constrains the direction of glucocorticoid receptor evolution. Nature 461(7263):515–519

    Article  Google Scholar 

  • Brown CT, Hug LA, Thomas BC et al (2015) Unusual biology across a group comprising more than 15% of domain Bacteria. Nature 523:208–211

    Article  Google Scholar 

  • Brunet TDP, Doolittle WF (2015) Multi-Level Selection Theory and the evolutionary functions of transposable elements. Genome Biol Evol 7(8):2445–2457

    Article  Google Scholar 

  • Cafarelli TM, Desbuleux A, Wang Y et al (2017) Mapping, modeling, and characterization of protein-protein interactions on a proteomic scale. Curr Opin Struct Biol 44:201–210

    Article  Google Scholar 

  • Clarke E (2016) Levels of selection in biofilms: multispecies biofilms are not evolutionary individuals. Biol Philos 31(20):191–212

    Article  Google Scholar 

  • Cohen DM, Steger DJ (2017) Nuclear receptor function through genomics: lessons from the glucocorticoid receptor. Trends Endocrinol Metab 28(7):531–540

    Article  Google Scholar 

  • Covello P, Gray M (1993) On the evolution of RNA editing. Trends Genet 9(8):265–268

    Article  Google Scholar 

  • Doolittle WF (1998) You are what you eat: a gene transfer ratchet could account for bacterial genes in eukaryotic nuclear genomes. Trends Genet 14(8):307–311

    Article  Google Scholar 

  • Doolittle WF (2013) Is junk DNA bunk? A critique of ENCODE. Proc Natl Acad Sci USA 110(14):5294–5300

    Article  Google Scholar 

  • Doolittle WF (2017) Darwinizing Gaia. J Theor Biol 434:11–19

    Article  Google Scholar 

  • Doolittle WF, Booth A (2017) It’s the song, not the singer: an exploration of holobiosis and evolutionary theory. Biol Philos 32(1):5–24

    Article  Google Scholar 

  • Doolittle WF, Sapienza C (1980) Selfish genes, the phenotype paradigm and genome evolution. Nature 284(5757):601–603

    Article  Google Scholar 

  • Doolittle WF, Luke J, Archibald JM, Keeling PJ, Gray MW (2011) Comment on “Does constructive neutral evolution play an important role in the origin of cellular complexity?”. BioEssays 33(6):427–429

    Article  Google Scholar 

  • Embley TM, Williams TA (2015) Evolution: steps on the road to eukaryotes. Nature 521(7551):169–170

    Article  Google Scholar 

  • Fedoroff NV (2012) Transposable elements, epigenetics, and genome evolution. Science 338(6108):758–767

    Article  Google Scholar 

  • Fernandez A, Lynch M (2011) Non-adaptive origins of interactome complexity. Nature 474:502–505

    Article  Google Scholar 

  • Finnigan GC, Hanson-Smith V, Stevens TH, Thornton JW (2012) Evolution of increased complexity in a molecular machine. Nature 481(7381):360–364

    Article  Google Scholar 

  • Frey-Wyssling A (1978) Concerning the concept ‘organelle’. Experientia 34(4):547

    Article  Google Scholar 

  • Fullmer MS, Soucy SM, Gogarten JP (2015) The pan-genome as a shared genomic resource: mutual cheating, cooperation and the black queen hypothesis. Front Microbiol 6:728

    Article  Google Scholar 

  • Giovannoni SJ, Thrash JC, Temperton B (2014) Implications of streamlining theory for microbial ecology. ISME J 8:1553–1565

    Article  Google Scholar 

  • Godfrey-Smith P (1994) A modern history theory of functions. Nous 28(3):344–362

    Article  Google Scholar 

  • Golding I, Cox EC (2006) Physical nature of bacterial cytoplasm. Phys Rev Lett 96(9):09810

    Article  Google Scholar 

  • Gould SJ (1989) Wonderful life: the Burgess shale and the nature of life. Norton, New York

    Google Scholar 

  • Gould SJ, Lewontin RC (1979) The spandrels of San Marco and the Panglossian paradigm: a critique of the adaptationist programme. Proc R Soc Lond B Biol Sci 205(1161):581–598

    Article  Google Scholar 

  • Gould SJ, Vrba ES (1982) Exaptation—a missing term in the science of form. Paleobiol 8(01):4–15

    Article  Google Scholar 

  • Gray MW, Lukeš J, Archibald JM, Keeling PJ, Doolittle WF (2010) Irremediable complexity? Science 330(6006):920–921

    Article  Google Scholar 

  • Grosche C, Funk HT, Maier UG, Zauner S (2012) The chloroplast genome of Pellia endiviifolia: gene content, RNA-editing pattern, and the origin of chloroplast editing. Genome Biol Evol 4(12):1349–1357

    Article  Google Scholar 

  • Hagstrom GI, Levin SA (2017) Marine ecosystems as complex adaptive systems: emergent patterns, critical transitions, and public goods. Ecosystems 20(3):458–476

    Article  Google Scholar 

  • Hartl F (2017) Protein misfolding diseases. In press, Ann Rev Biochem

    Google Scholar 

  • Hartwell LH, Hopfield JJ, Leibler S, Murray AW (1999) From molecular to modular cell biology. Nature 402(6761 Suppl):C47–C52

    Article  Google Scholar 

  • Hughes T, Ekman D, Ardawatia H, Elofsson A, Liberles DA (2007) Evaluating dosage compensation as a cause of duplicate gene retention in Paramecium tetraurelia. Genome Biol 8(5):213

    Article  Google Scholar 

  • Hutchison CA, Chuang R-Y, Noskov VN et al (2016) Design and synthesis of a minimal bacterial genome. Science 351(6280):aad6253

    Article  Google Scholar 

  • Ideker T, Galitski T, Hood L (2001) A new approach to decoding life: systems biology. Ann Rev Genomics Hum Genet 2:343–372

    Article  Google Scholar 

  • Jablonski D (2008) Species selection: theory and data. Ann Rev Ecol Evol Syst 39:501–524

    Article  Google Scholar 

  • Jacob F (1977) Evolution and tinkering. Science 196(4295):1161–1166

    Article  Google Scholar 

  • Jeffery CJ (2003) Moonlighting proteins: old proteins learning new tricks. Trends Genet 19(8):415–417

    Article  Google Scholar 

  • Kapusta A, Feschotte C (2014) Volatile evolution of long noncoding RNA repertoires: mechanisms and biological implications. Trends Genet 30(10):439–452

    Article  Google Scholar 

  • Keeling PJ, McCutcheon JP, Doolittle WF (2015) Symbiosis becoming permanent: survival of the luckiest. Proc Natl Acad Sci 112(33):10101–10103

    Article  Google Scholar 

  • Kidwell MG (2002) Transposable elements and the evolution of genome size in eukaryotes. Genetica 115(1):49–63

    Article  Google Scholar 

  • Kimura M (1983) The neutral theory of molecular evolution. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Koonin EV (2016) Splendor and misery of adaptation, or the importance of neutral null for understanding evolution. BMC Biol 14(1):114

    Article  Google Scholar 

  • Kuo CH, Moran NA, Ochman H (2009) The consequences of genetic drift for bacterial genome complexity. Genome Res 19(8):1450–1454

    Article  Google Scholar 

  • Lamech LT, Mallam AL, Lambowitz AM (2014) Evolution of RNA-protein interactions: non-specific binding led to RNA splicing activity of fungal mitochondrial tyrosyl-tRNA sythetases. PLoS Biol 12(12):e1002028

    Article  Google Scholar 

  • Landry CR, Levy ED, Rabbo DA, Tarassov K, Michnick SW (2013) Extracting insight from noisy cellular networks. Cell 155(5):983–989

    Article  Google Scholar 

  • Lane N, Martin W (2010) The energetics of genome complexity. Nature 467(7318):929–934

    Article  Google Scholar 

  • Lane N, Martin WF (2015) Eukaryotes really are special, and mitochondria are why. Proc Natl Acad Sci 112(35):E4823

    Article  Google Scholar 

  • Launay G, Ceres N, Martin J (2017) Non-interacting proteins may resemble interacting proteins: prevalence and implications. Sci Rep 7:40419

    Article  Google Scholar 

  • Lukeš J, Archibald JM, Keeling PJ, Doolittle WF, Gray MW (2011) How a neutral evolutionary ratchet can build cellular complexity. IUBMB Life 63(7):528–537

    Article  Google Scholar 

  • Lynch M, Conery JS (2000) The evolutionary fate and consequence of duplicate genes. Science 290:1151–1155

    Article  Google Scholar 

  • Lynch M, Force A (2000) The probability of duplicate gene preservation by subfunctionalization. Genetics 154(1):459–473

    Google Scholar 

  • Lynch M, Marinov GK (2017) Membranes, energetics, and evolution across the prokaryote-eukaryote divide. eLife 6:e20437

    Article  Google Scholar 

  • Majumder S, DeMott CM, Reverdatto S, Burz DS, Shektman A (2016) Total cellular RNA modulates protein activity. Biochemistry 55(32):4568–4573

    Article  Google Scholar 

  • Martin WF, Koonin EV (2006) Introns and the origin of nucleus-cytosol compartmentalization. Nature 440:41–45

    Article  Google Scholar 

  • Martiny AC, Treseder K, Pusch G (2013) Phylogenetic conservation of functional traits in microorganisms. ISME J 7:830–838

    Article  Google Scholar 

  • McShea DW, Brandon RN (2010) Biology’s first law: the tendency for diversity and complexity to increase in evolutionary systems. University of Chicago Press, Chicago

    Book  Google Scholar 

  • McShea DW, Venit EP (2001) What is a part. In: Wagner GP (ed) The character concept in evolutionary biology. Academic Press, London, pp 259–284

    Chapter  Google Scholar 

  • Mendoza E (2013) Organelle and functional module resources. In: Dubitzky W, Wolkenhauer O, Yokota H, Cho K-H (eds) Encyclopedia of systems biology. Springer, New York, pp. 1609–1611

    Chapter  Google Scholar 

  • Michod RE (1997) Cooperation and conflict in the evolution of individuality. I. Multilevel selection of the organism. Am Nat 149(4):607–645

    Article  Google Scholar 

  • Morris JJ, Lenski RE, Zinser ER (2012) The Black Queen Hypothesis: evolution of dependencies through adaptive gene loss. MBio 3(2):e00036–12

    Article  Google Scholar 

  • Newman ME (2006) Modularity and community structure in networks. Proc Natl Acad Sci 103(23):8577–8582

    Article  Google Scholar 

  • Novichkov PS, Wolf YI, Dubchak I, Koonin EV (2009) Trends in prokaryotic evolution revealed by comparison of closely related bacterial and archaeal genomes. J Bacteriol 191(1):65–73

    Article  Google Scholar 

  • O’Malley MA, Wideman JG, Ruiz-Trillo I (2016) Losing Complexity: the Role of Simplification in Macroevolution. Trends Ecol Evol 31(8):608–621

    Article  Google Scholar 

  • Okasha S (2005) Multilevel selection and the major transitions in evolution. Philos Sci 72(5):1013–1025

    Article  Google Scholar 

  • Omer S, Harlow TJ, Gogarten JP (2017) Does sequence conservation provide evidence for biological function? Trends Microbiol 25(1):11–18

    Article  Google Scholar 

  • Orgel LE, Crick FHC (1980) Selfish DNA: the ultimate parasite. Nature 284:604–607

    Article  Google Scholar 

  • Pande S, Kost C (2017) Bacterial unculturability and the formation of intercellular metabolic networks. Trends Microbiol 25(5):349–361

    Article  Google Scholar 

  • Rutherford SL (2003) Between genotype and phenotype: protein chaperones and evolvability. Nat Rev Genet 4:263–274

    Article  Google Scholar 

  • Sancar A (2008) The intelligent clock and the Rube Goldberg clock. Nat Struct Mol Biol 15(1):23–24

    Article  Google Scholar 

  • Simpson L, Thiemabb OH, Savill NJ, Alfonzo JD, Maslov DA (2000) Evolution of RNA editing in trypanosome mitochondria. Proc Natl Acad Sci USA 97:6986–6993

    Article  Google Scholar 

  • Sorrells TR, Johnson AD (2015) Making sense of transcription networks. Cell 161(4):714–723

    Article  Google Scholar 

  • Stoltzfus A (1999) On the possibility of constructive neutral evolution. J Mol Evol 49(2):169–181

    Article  Google Scholar 

  • Szathmary E, Smith JM (1995) Major transitions in evolution. Oxford University Press, Oxford

    Google Scholar 

  • Van Melderen L (2010) Toxin-antitoxin systems: why so many, what for? Curr Opin Microbiol 13(6):781–785

    Article  Google Scholar 

  • Varzi A (2016) Mereology. The Stanford encyclopedia of philosophy. Zalta EN (ed). https://plato.stanford.edu/archives/win2016/entries/mereology/. Accessed 7 Nov 2017

  • Wang Z, Zhang J (2007) In search of the biological significance of modular structures in protein networks. PLoS Comput Biol 3(6):e107

    Article  Google Scholar 

  • Wolf YI, Koonin EV (2013) Genome reduction as the dominant mode of evolution. BioEssays 35(9):829–837

    Article  Google Scholar 

  • Yang JR, Liao BY, Zhuang SM, Zhang J (2012) Protein misinteraction avoidance causes highly expressed proteins to evolve slowly. Proc Natl Acad Sci 109(14):E831–E840

    Article  Google Scholar 

  • Zuckerkandl E (1992) Revisiting junk DNA. J Mol Evol 34(3):259–271

    Article  Google Scholar 

Download references

Acknowledgements

We thank Dr. S. A. Inkpen, and the Dalhousie-Kings STS reading group for helpful comments, and NSERC Discovery Grant GLDSU 447989 for support.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to T. D. P. Brunet.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Brunet, T.D.P., Doolittle, W.F. The generality of Constructive Neutral Evolution. Biol Philos 33, 2 (2018). https://doi.org/10.1007/s10539-018-9614-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s10539-018-9614-6

Keywords

Navigation