Evolutionary developmental biology

Short description: Comparison of organism developmental processes

Homologous Hox genes in such different animals as insects and vertebrates control embryonic development and hence the form of adult bodies. These genes have been highly conserved through hundreds of millions of years of evolution.[1]

Evolutionary developmental biology, informally known as evo-devo, is a field of biological research that compares the developmental processes of different organisms to infer how developmental processes evolved.

The field grew from 19th-century beginnings, where embryology faced a mystery: zoologists did not know how embryonic development was controlled at the molecular level. Charles Darwin noted that having similar embryos implied common ancestry, but little progress was made until the 1970s. Then, recombinant DNA technology at last brought embryology together with molecular genetics. A key early discovery was that of homeotic genes that regulate development in a wide range of eukaryotes.

The field is composed of multiple core evolutionary concepts. One is deep homology, the finding that dissimilar organs such as the eyes of insects, vertebrates and cephalopod molluscs, long thought to have evolved separately, are controlled by similar genes such as pax-6, from the evo-devo gene toolkit. These genes are ancient, being highly conserved even across phyla; they generate the patterns in time and space which shape the embryo, and ultimately form the body plan of the organism. Another is that species do not differ much in their structural genes, such as those coding for enzymes; what does differ is the way that gene expression is regulated by the toolkit genes. These genes are reused, unchanged, many times in different parts of the embryo and at different stages of development, forming a complex cascade of control, switching other regulatory genes as well as structural genes on and off in a precise pattern. This multiple pleiotropic reuse explains why these genes are highly conserved, as any change would have many adverse consequences which natural selection would oppose.

New morphological features and ultimately new species are produced by variations in the toolkit, either when genes are expressed in a new pattern, or when toolkit genes acquire additional functions. Another possibility is the neo-Lamarckian theory that epigenetic changes are later consolidated at gene level, something that may have been important early in the history of multicellular life.

## Contents

* 1 History
* 1.1 Early theories
* 1.2 Recapitulation
* 1.3 Evolutionary morphology
* 1.4 The modern synthesis of the early 20th century
* 1.5 The lac operon
* 1.6 The birth of evo-devo and a second synthesis
* 2 The control of body structure
* 2.1 Deep homology
* 2.2 Gene toolkit
* 2.3 The embryo's regulatory networks
* 3 The origins of novelty
* 3.1 Variations in the toolkit
* 3.2 Consolidation of epigenetic changes
* 3.3 Developmental bias
* 4 Ecological evolutionary developmental biology
* 5 See also
* 6 Notes
* 7 References
* 7.1 Citations
* 7.2 Sources
* 8 External links

## History

### Early theories

Philosophers began to think about how animals acquired form in the womb in classical antiquity. Aristotle asserts in his Physics treatise that according to Empedocles, order "spontaneously" appears in the developing embryo. In his The Parts of Animals treatise, he argues that Empedocles' theory was wrong. In Aristotle's account, Empedocles stated that the vertebral column is divided into vertebrae because, as it happens, the embryo twists about and snaps the column into pieces. Aristotle argues instead that the process has a predefined goal: that the "seed" that develops into the embryo began with an inbuilt "potential" to become specific body parts, such as vertebrae. Further, each sort of animal gives rise to animals of its own kind: humans only have human babies.[2]

### Recapitulation

Main article: Biology:Recapitulation theory

Embryology theories of Ernst Haeckel, who argued for recapitulation[3] of evolutionary development in the embryo, and Karl Ernst von Baer's epigenesis

A recapitulation theory of evolutionary development was proposed by Étienne Serres in 1824–26, echoing the 1808 ideas of Johann Friedrich Meckel. They argued that the embryos of 'higher' animals went through or recapitulated a series of stages, each of which resembled an animal lower down the great chain of being. For example, the brain of a human embryo looked first like that of a fish, then in turn like that of a reptile, bird, and mammal before becoming clearly human. The embryologist Karl Ernst von Baer opposed this, arguing in 1828 that there was no linear sequence as in the great chain of being, based on a single body plan, but a process of epigenesis in which structures differentiate. Von Baer instead recognized four distinct animal body plans: radiate, like starfish; molluscan, like clams; articulate, like lobsters; and vertebrate, like fish. Zoologists then largely abandoned recapitulation, though Ernst Haeckel revived it in 1866.[4][5][6][7][8]

### Evolutionary morphology

A. Lancelet (a chordate), B. Larval tunicate, C. Adult tunicate. Kowalevsky saw that the notochord (1) and gill slits (5) are shared by tunicates and vertebrates.

From the early 19th century through most of the 20th century, embryology faced a mystery. Animals were seen to develop into adults of widely differing body plan, often through similar stages, from the egg, but zoologists knew almost nothing about how embryonic development was controlled at the molecular level, and therefore equally little about how developmental processes had evolved.[9] Charles Darwin argued that a shared embryonic structure implied a common ancestor. For example, Darwin cited in his 1859 book On the Origin of Species the shrimp-like larva of the barnacle, whose sessile adults looked nothing like other arthropods; Linnaeus and Cuvier had classified them as molluscs.[10][11] Darwin also noted Alexander Kowalevsky's finding that the tunicate, too, was not a mollusc, but in its larval stage had a notochord and pharyngeal slits which developed from the same germ layers as the equivalent structures in vertebrates, and should therefore be grouped with them as chordates.[10][12]

19th century zoology thus converted embryology into an evolutionary science, connecting phylogeny with homologies between the germ layers of embryos. Zoologists including Fritz Müller proposed the use of embryology to discover phylogenetic relationships between taxa. Müller demonstrated that crustaceans shared the Nauplius larva, identifying several parasitic species that had not been recognized as crustaceans. Müller also recognized that natural selection must act on larvae, just as it does on adults, giving the lie to recapitulation, which would require larval forms to be shielded from natural selection.[10] Two of Haeckel's other ideas about the evolution of development have fared better than recapitulation: he argued in the 1870s that changes in the timing (heterochrony) and changes in the positioning within the body (heterotopy) of aspects of embryonic development would drive evolution by changing the shape of a descendant's body compared to an ancestor's. It took a century before these ideas were shown to be correct.[13][14][15]

Turing's 1952 paper explained mathematically how patterns such as stripes and spots, as in the giant pufferfish, may arise, without molecular evidence.[16]

In 1917, D'Arcy Thompson wrote a book on the shapes of animals, showing with simple mathematics how small changes to parameters, such as the angles of a gastropod's spiral shell, can radically alter an animal's form, though he preferred a mechanical to evolutionary explanation.[17][18] But without molecular evidence, progress stalled.[10]

In 1952, Alan Turing published his paper "The Chemical Basis of Morphogenesis", on the development of patterns in animals' bodies. He suggested that morphogenesis could be explained by a reaction–diffusion system, a system of reacting chemicals able to diffuse through the body.[16] He modelled catalysed chemical reactions using partial differential equations, showing that patterns emerged when the chemical reaction produced both a catalyst (A) and an inhibitor (B) that slowed down production of A. If A and B then diffused at different rates, A dominated in some places, and B in others. The Russian biochemist Boris Belousov had run experiments with similar results, but was unable to publish them because scientists thought at that time that creating visible order violated the second law of thermodynamics.[19]

### The modern synthesis of the early 20th century

Main article: Biology:Modern synthesis (20th century)

In the so-called modern synthesis of the early 20th century, between 1918 and 1930 Ronald Fisher brought together Darwin's theory of evolution, with its insistence on natural selection, heredity, and variation, and Gregor Mendel's laws of genetics into a coherent structure for evolutionary biology. Biologists assumed that an organism was a straightforward reflection of its component genes: the genes coded for proteins, which built the organism's body. Biochemical pathways (and, they supposed, new species) evolved through mutations in these genes. It was a simple, clear and nearly comprehensive picture: but it did not explain embryology.[10][20] Sean B. Carroll has commented that had evo-devo's insights been available, embryology would certainly have played a central role in the synthesis.[1]

The evolutionary embryologist Gavin de Beer anticipated evolutionary developmental biology in his 1930 book Embryos and Ancestors,[21] by showing that evolution could occur by heterochrony,[22] such as in the retention of juvenile features in the adult.[13] This, de Beer argued, could cause apparently sudden changes in the fossil record, since embryos fossilise poorly. As the gaps in the fossil record had been used as an argument against Darwin's gradualist evolution, de Beer's explanation supported the Darwinian position.[23] However, despite de Beer, the modern synthesis largely ignored embryonic development to explain the form of organisms, since population genetics appeared to be an adequate explanation of how forms evolved.[24][25][lower-alpha 1]

### The lac operon

Main article: Biology:Lac operon

The lac operon. Top: repressed. Bottom: active. (1) RNA Polymerase, (2) Repressor, (3) Promoter, (4) Operator, (5) Lactose, (6–8) protein-encoding genes, controlled by the switch, that cause lactose to be digested.

In 1961, Jacques Monod, Jean-Pierre Changeux and François Jacob discovered the lac operon in the bacterium Escherichia coli. It was a cluster of genes, arranged in a feedback control loop so that its products would only be made when "switched on" by an environmental stimulus. One of these products was an enzyme that splits a sugar, lactose; and lactose itself was the stimulus that switched the genes on. This was a revelation, as it showed for the first time that genes, even in organisms as small as a bacterium, are subject to precise control. The implication was that many other genes were also elaborately regulated.[27]

### The birth of evo-devo and a second synthesis

In 1977, a revolution in thinking about evolution and developmental biology began, with the arrival of recombinant DNA technology in genetics, the book Ontogeny and Phylogeny by Stephen J. Gould and the paper "Evolution and Tinkering"[28] by François Jacob. Gould laid to rest Haeckel's interpretation of evolutionary embryology, while Jacob set out an alternative theory.[10] This led to a second synthesis,[29][30] at last including embryology as well as molecular genetics, phylogeny, and evolutionary biology to form evo-devo.[31][32] In 1978, Edward B. Lewis discovered homeotic genes that regulate embryonic development in Drosophila fruit flies, which like all insects are arthropods, one of the major phyla of invertebrate animals.[33] Bill McGinnis quickly discovered homeotic gene sequences, homeoboxes, in animals in other phyla, in vertebrates such as frogs, birds, and mammals; they were later also found in fungi such as yeasts, and in plants.[34][35] There were evidently strong similarities in the genes that controlled development across all the eukaryotes.[36] In 1980, Christiane Nüsslein-Volhard and Eric Wieschaus described gap genes which help to create the segmentation pattern in fruit fly embryos;[37][38] they and Lewis won a Nobel Prize for their work in 1995.[34][39]

Later, more specific similarities were discovered: for example, the distal-less gene was found in 1989 to be involved in the development of appendages or limbs in fruit flies,[40] the fins of fish, the wings of chickens, the parapodia of marine annelid worms, the ampullae and siphons of tunicates, and the tube feet of sea urchins. It was evident that the gene must be ancient, dating back to the last common ancestor of bilateral animals (before the Ediacaran Period, which began some 635 million years ago). Evo-devo had started to uncover the ways that all animal bodies were built during development.[41][42]

## The control of body structure

### Deep homology

Roughly spherical eggs of different animals give rise to distinct morphologies, from jellyfish to lobsters, butterflies to elephants. Many of these organisms share the same structural genes for body-building proteins like collagen and enzymes, but biologists had expected that each group of animals would have its own rules of development. The surprise of evo-devo is that the shaping of bodies is controlled by a rather small percentage of genes, and that these regulatory genes are ancient, shared by all animals. The giraffe does not have a gene for a long neck, any more than the elephant has a gene for a big body. Their bodies are patterned by a system of switching which causes development of different features to begin earlier or later, to occur in this or that part of the embryo, and to continue for more or less time.[9]

The puzzle of how embryonic development was controlled began to be solved using the fruit fly Drosophila melanogaster as a model organism. The step-by-step control of its embryogenesis was visualized by attaching fluorescent dyes of different colours to specific types of protein made by genes expressed in the embryo.[9] A dye such as green fluorescent protein, originally from a jellyfish, was typically attached to an antibody specific to a fruit fly protein, forming a precise indicator of where and when that protein appeared in the living embryo.[43]

The pax-6 gene controls development of eyes of different types across the animal kingdom.

Using such a technique, in 1994 Walter Gehring found that the pax-6 gene, vital for forming the eyes of fruit flies, exactly matches an eye-forming gene in mice and humans. The same gene was quickly found in many other groups of animals, such as squid, a cephalopod mollusc. Biologists including Ernst Mayr had believed that eyes had arisen in the animal kingdom at least 40 times, as the anatomy of different types of eye varies widely.[9] For example, the fruit fly's compound eye is made of hundreds of small lensed structures (ommatidia); the human eye has a blind spot where the optic nerve enters the eye, and the nerve fibres run over the surface of the retina, so light has to pass through a layer of nerve fibres before reaching the detector cells in the retina, so the structure is effectively "upside-down"; in contrast, the cephalopod eye has the retina, then a layer of nerve fibres, then the wall of the eye "the right way around".[44] The evidence of pax-6, however, was that the same genes controlled the development of the eyes of all these animals, suggesting that they all evolved from a common ancestor.[9] Ancient genes had been conserved through millions of years of evolution to create dissimilar structures for similar functions, demonstrating deep homology between structures once thought to be purely analogous.[45][46] This notion was later extended to the evolution of embryogenesis[47] and has caused a radical revision of the meaning of homology in evolutionary biology.[45][46][1]

### Gene toolkit

Main article: Biology:Evo-devo gene toolkit

Expression of homeobox (Hox) genes in the fruit fly

A small fraction of the genes in an organism's genome control the organism's development. These genes are called the developmental-genetic toolkit. They are highly conserved among phyla, meaning that they are ancient and very similar in widely separated groups of animals. Differences in deployment of toolkit genes affect the body plan and the number, identity, and pattern of body parts. Most toolkit genes are parts of signalling pathways: they encode transcription factors, cell adhesion proteins, cell surface receptor proteins and signalling ligands that bind to them, and secreted morphogens that diffuse through the embryo. All of these help to define the fate of undifferentiated cells in the embryo. Together, they generate the patterns in time and space which shape the embryo, and ultimately form the body plan of the organism. Among the most important toolkit genes are the Hox genes. These transcription factors contain the homeobox protein-binding DNA motif, also found in other toolkit genes, and create the basic pattern of the body along its front-to-back axis.[1] Hox genes determine where repeating parts, such as the many vertebrae of snakes, will grow in a developing embryo or larva.[9] Pax-6, already mentioned, is a classic toolkit gene.[48] Although other toolkit genes are involved in establishing the plant bodyplan,[49] homeobox genes are also found in plants, implying they are common to all eukaryotes.[50][51][52]

### The embryo's regulatory networks

A gene regulatory network

The protein products of the regulatory toolkit are reused not by duplication and modification, but by a complex mosaic of pleiotropy, i.e., being applied unchanged in many independent developmental processes, giving pattern to many dissimilar body structures.[1] The loci of these pleiotropic toolkit genes have large, complicated and modular cis-regulatory elements. For example, while a non-pleiotropic rhodopsin gene in the fruit fly has a cis-regulatory element just a few hundred base pairs long, the pleiotropic eyeless cis-regulatory region contains 6 cis-regulatory elements in over 7000 base pairs.[1] The regulatory networks involved are often very large. Each regulatory protein controls "scores to hundreds" of cis-regulatory elements. For instance, 67 fruit fly transcription factors controlled on average 124 target genes each.[1] All this complexity enables genes involved in the development of the embryo to be switched on and off at exactly the right times and in exactly the right places. Some of these genes are structural, directly forming enzymes, tissues and organs of the embryo. But many others are themselves regulatory genes, so what is switched on is often a precisely-timed cascade of switching, involving turning on one developmental process after another in the developing embryo.[1]

Gene product distributions along the long axis of the early embryo of a fruit fly

Such a cascading regulatory network has been studied in detail in the development of the fruit fly embryo. The young embryo is oval in shape, like a rugby ball. A small number of genes produce messenger RNAs that set up concentration gradients along the long axis of the embryo. In the early embryo, the bicoid and hunchback genes are at high concentration near the anterior end, and give pattern to the future head and thorax; the caudal and nanos genes are at high concentration near the posterior end, and give pattern to the hindmost abdominal segments. The effects of these genes interact; for instance, the Bicoid protein blocks the translation of caudal's messenger RNA, so the Caudal protein concentration becomes low at the anterior end. Caudal later switches on genes which create the fly's hindmost segments, but only at the posterior end where it is most concentrated.[53][54]

Gap genes in the fruit fly are switched on by genes such as bicoid, setting up stripes across the embryo which start to pattern the body's segments.

The Bicoid, Hunchback and Caudal proteins in turn regulate the transcription of gap genes such as giant, knirps, Krüppel, and tailless in a striped pattern, creating the first level of structures that will become segments.[37] The proteins from these in turn control the pair-rule genes, which in the next stage set up 7 bands across the embryo's long axis. Finally, the segment polarity genes such as engrailed split each of the 7 bands into two, creating 14 future segments.[53][54]

This process explains the accurate conservation of toolkit gene sequences, which has resulted in deep homology and functional equivalence of toolkit proteins in dissimilar animals (seen, for example, when a mouse protein controls fruit fly development). The interactions of transcription factors and cis-regulatory elements, or of signalling proteins and receptors, become locked in through multiple usages, making almost any mutation deleterious and hence eliminated by natural selection.[1]

The mechanism that sets up every animal's front-back axis is the same, implying a common ancestor. There is a similar mechanism for the back-belly axis for bilaterian animals, but it is reversed between arthropods and vertebrates.[55] Another process, gastrulation of the embryo, is driven by Myosin II molecular motors, which are not conserved across species. The process may have been started by movements of sea water in the environment, later replaced by the evolution of tissue movements in the embryo.[56][57][58]

## The origins of novelty

Among the more surprising and, perhaps, counterintuitive (from a neo-Darwinian viewpoint) results of recent research in evolutionary developmental biology is that the diversity of body plans and morphology in organisms across many phyla are not necessarily reflected in diversity at the level of the sequences of genes, including those of the developmental genetic toolkit and other genes involved in development. Indeed, as John Gerhart and Marc Kirschner have noted, there is an apparent paradox: "where we most expect to find variation, we find conservation, a lack of change".[59] So, if the observed morphological novelty between different clades does not come from changes in gene sequences (such as by mutation), where does it come from? Novelty may arise by mutation-driven changes in gene regulation.[1][60][61][62]

### Variations in the toolkit

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Variations in the toolkit may have produced a large part of the morphological evolution of animals. The toolkit can drive evolution in two ways. A toolkit gene can be expressed in a different pattern, as when the beak of Darwin's large ground-finch was enlarged by the BMP gene,[63] or when snakes lost their legs as distal-less became under-expressed or not expressed at all in the places where other reptiles continued to form their limbs.[64] Or, a toolkit gene can acquire a new function, as seen in the many functions of that same gene, distal-less, which controls such diverse structures as the mandible in vertebrates,[65][66] legs and antennae in the fruit fly,[67] and eyespot pattern in butterfly wings.[68] Given that small changes in toolbox genes can cause significant changes in body structures, they have often enabled the same function convergently or in parallel. distal-less generates wing patterns in the butterflies Heliconius erato and Heliconius melpomene, which are Müllerian mimics. In so-called facilitated variation,[69] their wing patterns arose in different evolutionary events, but are controlled by the same genes.[70] Developmental changes can contribute directly to speciation.[71]

### Consolidation of epigenetic changes

Main articles: Biology:Genetic assimilation and Transgenerational epigenetic inheritance

Evolutionary innovation may sometimes begin in Lamarckian style with epigenetic alterations of gene regulation or phenotype generation, subsequently consolidated by changes at the gene level. Epigenetic changes include modification of DNA by reversible methylation,[72] as well as nonprogrammed remoulding of the organism by physical and other environmental effects due to the inherent plasticity of developmental mechanisms.[73] The biologists Stuart A. Newman and Gerd B. Müller have suggested that organisms early in the history of multicellular life were more susceptible to this second category of epigenetic determination than are modern organisms, providing a basis for early macroevolutionary changes.[74]

### Developmental bias

Main article: Biology:Developmental bias

Among the centipedes, all members of the Geophilomorpha are constrained by a developmental bias to have an odd number of segments, whether as few as 27 or as many as 191.

Development in specific lineages can be biased either positively, towards a given trajectory or phenotype,[lower-alpha 2] or negatively, away from producing certain types of change; either may be absolute (the change is always or never produced) or relative. Evidence for any such direction in evolution is however hard to acquire and can also result from developmental constraints that limit diversification.[47] For example, in the gastropods, the snail-type shell is always built as a tube that grows both in length and in diameter; selection has created a wide variety of shell shapes such as flat spirals, cowries and tall turret spirals within these constraints. Among the centipedes, the Lithobiomorpha always have 15 trunk segments as adults, probably the result of a developmental bias towards an odd number of trunk segments. Another centipede order, the Geophilomorpha, the number of segments varies in different species between 27 and 191, but the number is always odd, making this an absolute constraint; almost all the odd numbers in that range are occupied by one or another species.[75][76][77]

## Ecological evolutionary developmental biology

Ecological evolutionary developmental biology, informally known as eco-evo-devo, integrates research from developmental biology and ecology to examine their relationship with evolutionary theory.[78] Researchers study concepts and mechanisms such as developmental plasticity, epigenetic inheritance, genetic assimilation, niche construction and symbiosis.[79][80]

## See also

* Arthropod head problem
* Cell signaling
* Evolution & Development (journal)
* Human evolutionary developmental biology
* Just So Stories (as seen by evolutionary developmental biologists)
* Plant evolutionary developmental biology
* Recapitulation theory

## Notes

1. ↑ Though C. H. Waddington had called for embryology to be added to the synthesis in his 1953 paper "Epigenetics and Evolution".[26]
2. ↑ Positive bias is sometimes called developmental drive.[75]

## References

### Citations

1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 Carroll, Sean B. (2008). "Evo-Devo and an Expanding Evolutionary Synthesis: A Genetic Theory of Morphological Evolution". Cell 134 (1): 25–36. doi:10.1016/j.cell.2008.06.030. PMID 18614008.
2. ↑ Leroi, Armand Marie (2014). The Lagoon: How Aristotle Invented Science. Bloomsbury. pp. 181–182. ISBN 978-1-4088-3622-4.
3. ↑ Richardson & Keuck 2002, p. 516
4. ↑ O'Connell, Lindsey (10 July 2013). "The Meckel-Serres Conception of Recapitulation". https://embryo.asu.edu/pages/meckel-serres-conception-recapitulation.
5. ↑ Desmond, Adrian J. (1989). The politics of evolution: morphology, medicine, and reform in radical London. Chicago: University of Chicago Press. pp. 53–53, 86–88, 337–340, 490–491. ISBN 978-0-226-14374-3. https://archive.org/details/politicsofevolut00adri/page/53.
6. ↑ Secord 2003, pp. 252–253
7. ↑ Bowler, Peter J. (2003). Evolution: the history of an idea. Berkeley: University of California Press. pp. 120–128, 190–191, 208. ISBN 978-0-520-23693-6. https://archive.org/details/evolutionhistory0000bowl_n7y8/page/120.
8. ↑ Secord 2003, pp. 424, 512
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10. ↑ 10.0 10.1 10.2 10.3 10.4 10.5 Gilbert, Scott F. (2003). "The morphogenesis of evolutionary developmental biology". International Journal of Developmental Biology 47 (7–8): 467–477. PMID 14756322. http://www.chd.ucsd.edu/_files/fall2008/Gilbert.2003.IJDB.pdf.
11. ↑ Darwin, Charles (1859). On the Origin of Species. London: John Murray. pp. 439–440. ISBN 978-0-8014-1319-3. http://darwin-online.org.uk/content/frameset?viewtype=text&itemID=F373&pageseq=457. "Cirripedes afford a good instance of this: even the illustrious Cuvier did not perceive that a barnacle was, as it certainly is, a crustacean; but a glance at the larva shows this to be the case in an unmistakeable manner."
12. ↑ Richmond, Marsha (January 2007). "Darwin's Study of the Cirripedia". Darwin Online. http://darwin-online.org.uk/EditorialIntroductions/Richmond_cirripedia.html.
13. ↑ 13.0 13.1 Hall, B. K. (2003). "Evo-Devo: evolutionary developmental mechanisms". International Journal of Developmental Biology 47 (7–8): 491–495. PMID 14756324.
14. ↑ Ridley, Mark (2003). Evolution. Wiley-Blackwell. ISBN 978-1-4051-0345-9. http://www.blackwellpublishing.com/ridley/.
15. ↑ Gould 1977, pp. 221–222.
16. ↑ 16.0 16.1 Turing, Alan M. (14 August 1952). "The Chemical Basis of Morphogenesis". Philosophical Transactions of the Royal Society of London B 237 (641): 37–72. doi:10.1098/rstb.1952.0012. Bibcode: 1952RSPTB.237...37T.
17. ↑ Ball, Philip (7 February 2013). "In retrospect: On Growth and Form". Nature 494 (32–33): 32–33. doi:10.1038/494032a. Bibcode: 2013Natur.494...32B.
18. ↑ Shalizi, Cosma. "Review: The Self-Made Tapestry by Philip Ball". University of Michigan. http://bactra.org/reviews/self-made-tapestry/.
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21. ↑ Held, Lewis I. (2014). How the Snake Lost its Legs. Curious Tales from the Frontier of Evo-Devo. Cambridge University Press. p. 67. ISBN 978-1-107-62139-8.
22. ↑ Gould 1977, pp. 221–222
23. ↑ Brigandt, Ingo (2006). "Homology and heterochrony: the evolutionary embryologist Gavin Rylands de Beer (1899-1972)". Journal of Experimental Zoology 306B (4): 317–328. doi:10.1002/jez.b.21100. PMID 16506229. Bibcode: 2006JEZB..306..317B. https://www.ualberta.ca/~brigandt/de_Beer.pdf.
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25. ↑ Adams, M. (1991). "Through the looking glass: The evolution of Soviet Darwinism". in Warren, L.. New Perspectives in Evolution. Liss/Wiley. pp. 37–63.
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27. ↑ Monod, Jacques; Changeux, J.P.; Jacob, François (1963). "Allosteric proteins and cellular control systems". Journal of Molecular Biology 6 (4): 306–329. doi:10.1016/S0022-2836(63)80091-1. PMID 13936070. Bibcode: 1963JMBio...6..306M.
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31. ↑ Goodman, C. S.; Coughlin, B. C. (2000). "Special feature: The evolution of evo-devo biology". Proceedings of the National Academy of Sciences 97 (9): 4424–4456. doi:10.1073/pnas.97.9.4424. PMID 10781035. Bibcode: 2000PNAS...97.4424G.
32. ↑ Müller GB and Newman SA (Eds.) (2005). "Special issue: Evolutionary Innovation and Morphological Novelty". Journal of Experimental Zoology Part B 304B (6): 485–631. doi:10.1002/jez.b.21080. PMID 16252267. http://www3.interscience.wiley.com/cgi-bin/jissue/112149101.
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34. ↑ 34.0 34.1 Winchester, Guil (2004). "Edward B. Lewis 1918-2004". Current Biology 14 (18): R740–742. Sep 21, 2004. doi:10.1016/j.cub.2004.09.007. PMID 15380080. Bibcode: 2004CBio...14.R740W. http://www.cell.com/current-biology/pdf/S0960-9822(04)00683-9.pdf.
35. ↑ Bürglin, Thomas R.. "The Homeobox Page". Karolinska Institutet. http://homeobox.biosci.ki.se/.
36. ↑ Holland, P.W. (2013). "Evolution of homeobox genes". Wiley Interdiscip Rev Dev Biol 2 (1): 31–45. doi:10.1002/wdev.78. PMID 23799629. "Homeobox genes are found in almost all eukaryotes, and have diversified into 11 gene classes and over 100 gene families in animal evolution, and 10 to 14 gene classes in plants.".
37. ↑ 37.0 37.1 Nüsslein-Volhard, C.; Wieschaus, E. (October 1980). "Mutations affecting segment number and polarity in Drosophila". Nature 287 (5785): 795–801. doi:10.1038/287795a0. PMID 6776413. Bibcode: 1980Natur.287..795N.
38. ↑ Arthur, Wallace (14 February 2002). "The emerging conceptual framework of evolutionary developmental biology". Nature 415 (6873): 757–764. doi:10.1038/415757a. PMID 11845200. Bibcode: 2002Natur.415..757A.
39. ↑ "Eric Wieschaus and Christiane Nüsslein-Volhard: Collaborating to Find Developmental Genes". iBiology. https://www.ibiology.org/ibiomagazine/eric-wieschaus-and-christiane-nusselin-volhard.html.
40. ↑ Cohen, S. M.; Jurgens, G. (1989). "Proximal-distal pattern formation in Drosophila: cell autonomous requirement for Distal-less activity in limb development". EMBO J. 8 (7): 2045–2055. doi:10.1002/j.1460-2075.1989.tb03613.x. PMID 16453891.
41. ↑ Carroll, Sean B. (2006). Endless Forms Most Beautiful: The New Science of Evo Devo and the Making of the Animal Kingdom. Weidenfeld & Nicolson [Norton]. pp. 63–70. ISBN 978-0-297-85094-6.
42. ↑ Panganiban, G.; Irvine, S. M.; Lowe, C.; Roehl, H.; Corley, L. S.; Sherbon, B.; Grenier, J. K.; Fallon, J. F. et al. (1997). "The origin and evolution of animal appendages". Proceedings of the National Academy of Sciences of the United States of America 94 (10): 5162–5166. doi:10.1073/pnas.94.10.5162. PMID 9144208. Bibcode: 1997PNAS...94.5162P.
43. ↑ "Fluorescent Probes". ThermoFisher Scientific. 2015. https://www.thermofisher.com/uk/en/home/life-science/protein-biology/protein-biology-learning-center/protein-biology-resource-library/pierce-protein-methods/fluorescent-probes.html#.
44. ↑ Land, M. F.; Fernald, R. D. (1992). "The evolution of eyes". Annual Review of Neuroscience 15: 1–29. doi:10.1146/annurev.ne.15.030192.000245. PMID 1575438.
45. ↑ 45.0 45.1 Tomarev, Stanislav I.; Callaerts, Patrick; Kos, Lidia; Zinovieva, Rina; Halder, Georg; Gehring, Walter; Piatigorsky, Joram (1997). "Squid Pax-6 and eye development". Proceedings of the National Academy of Sciences 94 (6): 2421–2426. doi:10.1073/pnas.94.6.2421. PMID 9122210. Bibcode: 1997PNAS...94.2421T.
46. ↑ 46.0 46.1 Pichaud, Franck; Desplan, Claude (August 2002). "Pax genes and eye organogenesis". Current Opinion in Genetics & Development 12 (4): 430–434. doi:10.1016/S0959-437X(02)00321-0. PMID 12100888.
47. ↑ 47.0 47.1 Drost, Hajk-Georg; Janitza, Philipp; Grosse, Ivo; Quint, Marcel (2017). "Cross-kingdom comparison of the developmental hourglass". Current Opinion in Genetics & Development 45: 69–75. doi:10.1016/j.gde.2017.03.003. PMID 28347942.
48. ↑ Xu, P.X.; Woo, I.; Her, H.; Beier, D. R.; Maas, R. L. (1997). "Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode". Development 124 (1): 219–231. doi:10.1242/dev.124.1.219. PMID 9006082.
49. ↑ Quint, Marcel; Drost, Hajk-Georg; Gabel, Alexander; Ullrich, Kristian Karsten; Bönn, Markus; Grosse, Ivo (2012-10-04). "A transcriptomic hourglass in plant embryogenesis". Nature 490 (7418): 98–101. doi:10.1038/nature11394. ISSN 0028-0836. PMID 22951968. Bibcode: 2012Natur.490...98Q.
50. ↑ Mukherjee, K.; Brocchieri, L.; Bürglin, T.R. (December 2009). "A comprehensive classification and evolutionary analysis of plant homeobox genes". Molecular Biology and Evolution 26 (12): 2775–94. doi:10.1093/molbev/msp201. PMID 19734295.
51. ↑ Bürglin, T.R. (November 1997). "Analysis of TALE superclass homeobox genes (MEIS, PBC, KNOX, Iroquois, TGIF) reveals a novel domain conserved between plants and animals". Nucleic Acids Research 25 (21): 4173–80. doi:10.1093/nar/25.21.4173. PMID 9336443.
52. ↑ Derelle, R.; Lopez, P.; Le Guyader, H.; Manuel, M. (2007). "Homeodomain proteins belong to the ancestral molecular toolkit of eukaryotes". Evolution & Development 9 (3): 212–9. doi:10.1111/j.1525-142X.2007.00153.x. PMID 17501745.
53. ↑ 53.0 53.1 Russel, Peter (2010). iGenetics: a molecular approach. Pearson Education. pp. 564–571. ISBN 978-0-321-56976-9.
54. ↑ 54.0 54.1 Rivera-Pomar, Rolando; Jackle, Herbert (1996). "From gradients to stripes in Drosophila embryogenesis: Filling in the gaps". Trends in Genetics 12 (11): 478–483. doi:10.1016/0168-9525(96)10044-5. PMID 8973159.
55. ↑ De Robertis, Eddy; Sasai, Yoshiki (1996). "A common plan for dorsoventral patterning in Bilateria". Nature 380 (6569): 37–40. doi:10.1038/380037a0. PMID 8598900. Bibcode: 1996Natur.380...37D.
56. ↑ Farge, Emmanuel (2003). "Mechanical induction of twist in the Drosophila foregut/stomodeal primordium". Current Biology 13 (16): 1365–1377. doi:10.1016/s0960-9822(03)00576-1. PMID 1293230. Bibcode: 2003CBio...13.1365F.
57. ↑ Nguyen, Ngoc-Minh et al. (2022). "Mechano-biochemical marine stimulation of inversion, gastrulation, and endomesoderm specification in multicellular Eukaryota". Frontiers in Cell and Developmental Biology 10. doi:10.3389/fcell.2022.992371. PMID 36531949.
58. ↑ Nguyen, Ngoc-Minh et al. (2024). "Mechanical induction in metazoan development and evolution: from earliest multi-cellular organisms to modern animal embryos". Nature Communications 15 (1). doi:10.1038/s41467-024-55100-5. PMID 39702750. Bibcode: 2024NatCo..1510695N.
59. ↑ Gerhart, John; Kirschner, Marc (1997). Cells, Embryos and Evolution. Blackwell Science. ISBN 978-0-86542-574-3.
60. ↑ Carroll, Sean B.; Grenier, Jennifer K.; Weatherbee, Scott D. (2005). From DNA to Diversity: Molecular Genetics and the Evolution of Animal Design — Second Edition. Blackwell Publishing. ISBN 978-1-4051-1950-4.
61. ↑ Carroll, Sean B. (2000). "Endless forms: the evolution of gene regulation and morphological diversity". Cell 101 (6): 577–80. doi:10.1016/S0092-8674(00)80868-5. PMID 10892643.
62. ↑ Moczek, Armin P. (2015). "The Significance and Scope of Evolutionary Developmental Biology: A Vision for the 21st Century". Evolution & Development 17 (3): 198–219. doi:10.1111/ede.12125. PMID 25963198. Bibcode: 2015EvDev..17..198M. http://www.extavourlab.com/pdfs/papers/2015_Moczek_EvolDev.pdf. Retrieved 27 November 2015.
63. ↑ Abzhanov, A.; Protas, M.; Grant, B.R.; Grant, P.R.; Tabin, C.J. (2004). "Bmp4 and Morphological Variation of Beaks in Darwin's Finches". Science 305 (5689): 1462–1465. doi:10.1126/science.1098095. PMID 15353802. Bibcode: 2004Sci...305.1462A.
64. ↑ Cohn, M.J.; Tickle, C. (1999). "Developmental basis of limblessness and axial patterning in snakes". Nature 399 (6735): 474–479. doi:10.1038/20944. PMID 10365960. Bibcode: 1999Natur.399..474C.
65. ↑ Beverdam, A.; Merlo, G.R.; Paleari, L.; Mantero, S.; Genova, F.; Barbieri, O.; Janvier, P.; Levi, G. (August 2002). "Jaw Transformation With Gain of Symmetry After DLX5/DLX6 Inactivation: Mirror of the Past?". Genesis 34 (4): 221–227. doi:10.1002/gene.10156. PMID 12434331. https://iris.unito.it/bitstream/2318/87307/1/Beverdam_2002.pdf.
66. ↑ Depew, M.J.; Lufkin, T.; Rubenstein, J.L. (October 2002). "Specification of jaw subdivisions by DLX genes". Science 298 (5592): 381–385. doi:10.1126/science.1075703. PMID 12193642. Bibcode: 2002Sci...298..381D.
67. ↑ Panganiban, Grace; Rubenstein, John L. R. (2002). "Developmental functions of the Distal-less/Dlx homeobox genes". Development 129 (19): 4371–4386. doi:10.1242/dev.129.19.4371. PMID 12223397. http://dev.biologists.org/content/129/19/4371.
68. ↑ Beldade, P.; Brakefield, P.M.; Long, A.D. (2002). "Contribution of Distal-less to quantitative variation in butterfly eyespots". Nature 415 (6869): 315–318. doi:10.1038/415315a. PMID 11797007.
69. ↑ Gerhart, John; Kirschner, Marc (2007). "The theory of facilitated variation". Proceedings of the National Academy of Sciences 104 (suppl1): 8582–8589. doi:10.1073/pnas.0701035104. PMID 17494755. Bibcode: 2007PNAS..104.8582G.
70. ↑ Baxter, S.W.; Papa, R.; Chamberlain, N.; Humphray, S.J.; Joron, M.; Morrison, C.; ffrench-Constant, R.H.; McMillan, W.O. et al. (2008). "Convergent Evolution in the Genetic Basis of Mullerian Mimicry in Heliconius Butterflies". Genetics 180 (3): 1567–1577. doi:10.1534/genetics.107.082982. PMID 18791259. Bibcode: 2008Genet.180.1567B.
71. ↑ Pennisi, E. (2002). "Evolutionary Biology:Evo-Devo Enthusiasts Get Down to Details". Science 298 (5595): 953–955. doi:10.1126/science.298.5595.953. PMID 12411686.
72. ↑ Jablonka, Eva; Lamb, Marion (1995). Epigenetic Inheritance and Evolution: The Lamarckian Dimension. Oxford, New York: Oxford University Press. ISBN 978-0-19-854063-2.
73. ↑ West-Eberhard, Mary Jane (2003). Developmental plasticity and evolution. New York: Oxford University Press. ISBN 978-0-19-512235-0.
74. ↑ Müller, Gerd B., ed (2003). Origination of Organismal Form: Beyond the Gene in Developmental and Evolutionary Biology. MIT Press.
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### Sources

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* Smocovitis, Vassiliki Betty (1996). Unifying Biology: The Evolutionary Synthesis and Evolutionary Biology. Princeton, NJ: Princeton University Press. ISBN 978-0-691-03343-3. OCLC 34411399.
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